Abstract
The differential diagnosis of arthritis is exhaustive (see table of contents; Chapter 2). The 1988 edition of the Primer on the Rheumatic Diseases,1 prepared by a committee of the American College of Rheumatology (ACR), lists over 100 disorders in which arthritis may be a significant manifestation. A few of these conditions have not yet been reported in children. We have also found it necessary to add to this exhaustive list. Several additional disorders were recently first seen in children in our own clinic, and there continue to be new additions to this list each year.
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References
Schumacher HR Jr, Klippel JH, Robinson DR: Primer on the Rheumatic Diseases, 9th ed. Arthritis Foundation, Atlanta, GA, 1988, pp. 1–355.
Markowitz M, Gordis L: Rheumatic Fever, 2nd ed. Saunders, Philadelphia, 1972.
Pope RM: Rheumatic fever in the 1980’s. Bull Rheum Dis 38: 1–8, 1989.
Griffiths SP, Gersony WM: Acute rheumatic fever in New York City (1969 to 1988): A comparative study of two decades. J Pediatr 116: 882–887, 1990.
Zangwill KM, Wald ER, Londino AV Jr.: Acute rheumatic fever in western Pennsylvania: A persistent problem into the 1990’s. J Pediatr 118: 561–563, 1991.
Wallace MR, Garst PD, Papadimos TJ, Oldifeld EC III: The return of acute rheumatic fever in young adults. JAMA 262: 2557–2561, 1989.
Hicks R, Yim G: Post-Streptococcal Reactive Arthritis (PSRA)-A Manifestation of Acute Rheumatic Fever (ARF). Arthritis Rheum 33: 5145, 1990.
Kusala GA, Doshi H, Brick JE: Rheumatic fever and post-streptococcal glomerulonephritis: A case report. Arthritis Rheum 32: 236–239, 1989.
Raz I, Fisher J, Israeli A, et al.: An unusual case of rheumatic pneumonia. Arch Intern Med 145: 1130–1131, 1985.
De Cunto CL, Giannini EH, Fink CW, et al.: Prognosis of children with post-streptococcal reactive arthritis. Pediatr Infect Dis J 7: 683–686, 1988.
Wilson MG: Rheumatic Fever. The Commonwealth Fund, New York, 1940.
Crea MA, Mortimer EA Jr: The nature of scarlatinal arthritis. Pediatrics 23: 879–884, 1959.
Austin III HA, Balow JE, Henoch-Schonlein Nephritis: Prognostic features and the challenge of therapy. Am J Kid Dis 2: 512–520, 1983.
Olson JC, Kelly KJ, Pan CG, Wortmann DW. Pulmonary disease with hemorrhage in Henoch-Schonlein purpura. Pediatrics 89: 1177–1181, 1992.
Stewart M, Savage JM, Bell B, McCord B: Long term renal prognosis of Henoch-Schonlein purpura in an unselected childhood population. Eur J Pediatr 147: 113–115, 1988.
Blomgren SE: Erythema nodosum. Semin Arthritis Rheum 4: 1–24, 1974.
Spear JB, Kessler HA, Dworin A, Semel J: Erythema Nodosum Associated with Acute Cytomegalovirus Mononucleosis in an adult. Arch Intern Med 148: 323324, 1988.
Weston WL, Brice SL, Jester JD, Lane AT, et al.: Herpes Simplex virus in childhood erythema multiforme. Pediatrics 89: 32–4, 1992.
Kunnamo I, Kallio P, Pelkonen P, Viander M: Serum-sickness-like disease is a common cause of acute arthritis in children. Acta Paediatr Scand 75: 964–967, 1986.
Heckbert SR, Stryker WS, Coltin KL, et al.: Serum sickness in children after antibiotic exposure: Estimates of occurrence and morbidity in a health maintenance organization population. Am J Epidemiol 132: 336–342, 1990.
Rasmussen JE: Update on the Stevens Johnson syndrome. Clev Clin J Med 55:412–413, 1988 (see also pp. 467–469).
Levy M, Shear NH: Mycoplasma pneumoniae infections and Stevens Johnson syndrome. Report of eight cases and review of the literature. Clin Ped 30: 42–49, 1991.
Prendiville JS, Herbert AA, Greenwald MJ, Esterly NB: Management of Stevens Johnson syndrome and toxic epidermal necrolysis in children. J Pediatr 155: 881–887, 1989.
Gern JE, Yang E, Evrard HM, Sampson HA: Allergic reactions to milk-contaminated “nondairy” products. N Eng J Med 324: 976–979, 1991.
Olson JC, Esterly NB: Urticarial vasculitis and Lyme disease. J Am Acad Der-matol 22: 1114–1116, 1990.
b.Massarotti EM, Liu NY, Mier J, Atkins MB. Chronic inflammatory arthritis after treatment with high-dose Interleukin-2 for malignancy. Am J Med 92: 693–697, 1992.
Braverman IM: Skin Signs of Systemic Disease. Saunders, Philadelphia, 1981, pp. 444–452.
Longley J, Demar L, Feinstein RP, et al.: Clinical and histologic features of pityriasis lichenoides et varioliformis acuta in children. Arch Dermatol 123: 1335–1339, 1987.
Baron F, Sybert VP, Andrews RG: Cutaneous and extracutaneous neutrophilic infiltrates (Sweet Syndrome) in three patients with Fanconi anemia. J Pediatr 115: 726–729, 1989.
Moreland LW, Brick JE, Kovach RE, et al.: Acute febrile neutrophilic dermatosis (Sweet Syndrome): A review of the literature with emphasis on muscloskeletal manifestations. Semin Arthritis Rheum 17, 3: 143–155, 1988.
Jorizzo JL, Solomon AR, Zanolli MD, Leshin B: Neutrophilic vascular reactions. J Am Acad Dermatol 19: 983–1005, 1988.
Majeed HA, Kalaawi M, Mohanty D, et al.: Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children. J Pediatr 115: 730–734, 1989.
Yu L, Kasser JR, O’Rourke E, et al.: Chronic Recurrent Multifocal Osteomyelitis. J Bone Jt Surg 71-A: 105–112, 1989.
Cho KH, Shin KS, Sohn SJ: Behcet’s disease with Sweet’s syndrome-like presentation—A report of six cases. Clin Exp Dermatol 14: 20–24, 1989.
Webb JG, Butany J, Langer G, et al.: Myocarditis and myocardial hemorrhage associated with thrombotic thrombocytopenic purpura. Arch Intern Med 150: 1535–1537, 1990.
Onundarson PT, Rowe JM, Heal JM, Francis CW. Response to plasma exchange and splenectomy in thrombotic thrombocytopenic purpura. Arch Int Med 152: 791–796, 1992.
Bell WR, Braine HG, Ness PM, Kickler TS: Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical Experience in 108 Patients. N Eng J Med 325:398–403, 1991. (See also: Editorial pp. 426427).
Jacobs JC: Acute osteomyelitis; medical management in children NY State J Med 78: 910–912, 1978.
Shulman, ST, Ayoub EM: Severe staphylococcal sepsis in adolescents. Pediatrics 58: 59–66, 1976.
Hieber JP, Nelson AJ, McCracken GH: Acute disseminated staphylococcal disease in childhood. Am J Dis Child 131: 181–185, 1977.
Dich VD, Nelson JD, Haltalin KC: Osteomyelitis in infants and children. Am J Dis Child 129: 1273–1278, 1975.
Edwards MS, Baker CJ, Granberry WM, Barrent FF: Pelvic osteomyelitis in children Pediatrics 61: 63–67, 1978.
Nolla-Solé JM, Mateo-Soria L, Rozadilla-Sacanell A, et al.: Role of technetium-99m diphosphonate and gallium-67 citrate bone scanning in the early diagnosis of infectious spondylodiscitis. A comparative study. Ann Rheum Dis 51: 665667, 1992.
Lisbona R, Rosenthal) L: Observations on the sequential use of 99mTcphosphate complex and 67Ga imaging in osteomyelitis, cellulitis, and septic arthritis. Radiology 123: 123–129, 1977.
Sullivan DC, Rosenfield NS, Ogden J, et al.: Problems in the scintigraphic detection of osteomyelitis in children. Radiology 135: 731–736, 1980.
Handmaker H: Acute hematogenous osteomyelitis: Has the bone scan betrayed us? Radiology 135: 787–789, 1980.
Fleisher GR, Paradise JE, Plotkin SA, et al.: Falsely normal radiouclide scans for osteomyelitis. Am J Dis Child 134: 499–502, 1980.
Tetzlaff TR, McCracken GH, Nelson, JD: Oral antibiotic therapy for skeletal infections of children. II. Therapy of osteomyelitis and suppurative arthritis. J Pediatr 92: 485–490, 1978.
Nelson JD: A critical review of the role of oral antibiotics in the management of hematogenous osteomyelitis. In: Remington JS, Swartz MN (eds.) Current Clinical Topics in infectious diseases 4. McGraw-Hill, New York, pp. 64–74, 1983.
Blockey, NJ, Watson JT: Acute osteomyelitis in children. J Bone Joint Surg 52B: 77–87, 1970.
Kolyvas E, Ahronheim IG, Marks MI, et al.: Oral antibiotic therapy of skeletal infections in children. Pediatrics 65: 867–871, 1980.
Dangles CJ: Two unusual presentations of pyogenic sacroiliitis. Orthopaedic Review 16: 77–80, 1987.
Schaad UB, McCracken GH, Nelson JD: Pyogenic arthritis of the sacroiliac joint in pediatric patients. Pediatrics 66: 375–379, 1980.
Reilly JP, Gross RH, Emans JB, et al.: Disorders of the sacroiliac joint in children J Bone Joint Surg 70A: 31–40, 1988.
Milgrom C, Kaplan L, Fields S, et al.: Osteolytic osteogenic sarcoma of ilium in a 46 month old boy. Ortho Rev 16: 187–189, 1987.
Cabanela ME, Sim FH, Beabour JW, Dahlin DC: Osteomyelitis appearing as neoplasms; a diagnostic problem. Arch Surg 109: 68–72, 1974.
Fisher MC, Goldsmith JF, Gilligan PH: Sneakers as a source of Pseudomonas aeruginosa in children with osteomyelitis following puncture wounds. J Pediatr 106: 607–609, 1985.
Congeni BL, Weiner DS, Izsak E: Expanded spectrum of organisms causing osteomyelitis after puncture wounds of the foot. Orthopedics 4: 531–533, 1981.
Harrison CJ, Kiely L, Fowler SL: Puncture wounds of the foot. Pediatr Res 25S: 180A, 1989.
Subbarao EK, Tarpay MM, Marks MI: Soft-tissue infections caused by Mycobacterium fortuitum complex following penetrating injury. Am J Dis Child 141: 1018–1020, 1987.
Wadlington WB, Hatcher H, Turner DJ: Osteomyelitis of the patella. Clin Pediatr 10: 577–580, 1971.
Ho G, Tice AD, Kaplan SR: Septic bursitis in the prepatellar and olecranon bursae. Ann Int Med 89: 21–27, 1978.
Raddatz DA, Hoffman GS, Franck WA: Septic Bursitis: Presentation, treatment and prognosis. J Rheumatol 14: 1160–1163, 1987.
Pien FD, Ching D, Kim E: Septic Bursitis: Experience in a community practice. Orthopedics 14: 981–984, 1991.
March AW, Riley LH, Robinson RA: Retroperitoneal abscess and septic arthritis of the hip in children. J Bone Joint Surg 54A: 67–74, 1972.
Maull KI, Sachatello CR: Retroperitional iliac fossa abscess; a complication of suppurative iliac lymphadenitis. Am J Surg 127: 270–274, 1974.
Stefanich RJ, Moskowitz A: Hip flexion deformity secondary to acute pyogenic psoas abscess. Orthopaed Rev 16: 25–35, 1987.
Korobkin M, Callen PW, Filly RA, et al.: Comparison of computed tomography, ultrasonography, and gallium-67 scanning in the evaluation of suspected abdominal masses. Radiology 129: 89–93, 1978.
Taylor KJW, Sullivan DC, Wasson JFM, et al.: Ultrasound and gallium for the diagnosis of abdominal and pelvic abscesses. Gastrointest Radiol 3: 281–286, 1978.
Sirinavin S, McCracken GH Jr.: Primary suppurative myositis in children. Am J Dis Child 133: 263–265, 1979.
Beavers BR: Fusobacterium Nucleatum Pyomyositis. Orthopedics 15: 208–211, 1992.
Minor RL, Baum S, Schulze-Delrieu KS: Pyomyositis in a patient with progressive systemic sclerosis: case report and review of the literature. Arch Intern Med 148: 1453–1455, 1988.
Yuh WTC, Schreiber AE, Montgomery WJ, Ehara S: Magnetic resonance imaging of pyomyositis. Skeletal Radiol 17: 190–193, 1988.
Swarts RL, Martinez LA, Robson HG: Gonococcal pyomyositis. JAMA 246: 246, 1981.
Fleckenstein JL, Burns DK, Murphy FK, et al. Differential diagnosis of bacterial myositis in AIDS: evaluation with MR imaging. Radiology 179: 653–658, 1992.
Rotbart HA, Glode MP: Haemophilus influenzae type b septic arthritis in children: Report of 23 cases. Pediatrics 75: 254–259, 1985.
Taylor TKF, Bye WA: Role of antibiotics in inflammatory disc lesions in children. Lancet 2: 881–882, 1977.
Fischer GW, Popich GA, Sullivan DE, et al.: Diskitis: A prospective diagnostic analysis. Pediatrics 62: 543–548, 1978.
Bolivar R, Kohl S, Pickering LK: Vertebral osteomyelitis in children: Report of four cases. Pediatrics 62: 549–553, 1978.
Wenger DR, Bobechko WP, Gilday DL: The spectrum of intervertebral disc-space infection in children. J Bone Joint Surg 60A: 100–108, 1979.
Waldvogel FA, Vasey H: Osteomyelitis: The past decade. N Engl J Med 303: 360–370, 1980.
Boscamp JR, Steigbigel NH: Disk space infection. In: Orthopedic infection, Schlossberg D (ed.) Springer-Verlag, New York, pp. 49–68, 1988.
Meyers SP, Wiener SN: Diagnosis of hematogenous pyogenic vertebral osteomyelitis by Magnetic Resonance Imaging. Arch Intern Med 151: 683–687, 1991
Bjorksten B, Gustayson KH, Eriksson B, et al.: Chronic recurrent multifocal osteomyelitis and pustular palmoplantaris. J Pediatr 93: 227–231, 1978.
Van Howe RS, Starshak RJ, Chusid MJ: Chronic, recurrent multifocal osteomyelitis. Case report and review of the literature. Clin Pediatr 28: 54–59, 1989.
Mortensson W, Edeburn G, Fires M, Nilsson R: Chronic recurrent multifocal osteomyelitis in children. A roentgenologic and scintigraphic investigation. Acta Radiol 29: 565–570, 1988.
Yu L, Kasser JR, O’Rourke E, et al.: Chronic recurrent multifocal osteomyelitis. J Bone Jt Surg 71-A: 105–112, 1989.
Berney S, Goldstein M, Bishko F: Clinical and diagnostic features of tuberculous arthritis. Am J Med 53: 36–42, 1972.
Wallace R, Cohen AS: Tuberculous arthritis. Am J Med 61: 277–282, 1976.
Sutker WL, Lankford LL, Tompsett R: Granulomatous synovitis: The role of atypical mycobacteria. Rev Infect Dis 1: 729–735, 1979.
Jacobs, JC, Phillips PE, Johnston AD, Needle biopsy of the synovium of children. Pediatrics 57: 696–701, 1976.
Southwood RT, Hancock EJ, Petty RE, et. al: Tuberculous rheumatism (Poncet’s disease) in a child. Arthritis Rheum 31: 1311–1313, 1988.
Arnow PM, Smaron M, Ormiste V: Brucellosis in a group of travelers to Spain. JAMA 251: 505–508, 1984.
Lubani M, Sharda D, Helin I: Brucella arthritis in children. Infection 14: 233236, 1986.
Lubani MM, Dudin KI, Sharda DC, et al.: A multicenter therapeutic study of 1100 children with brucellosis. Pediatr Infect Dis J 8: 75–78, 1989.
Diggs LW: Bone and joint lesions in sickle-cell disease. Clin Orthop 52: 119143, 1967.
Collipp PJ, Koch R: Cat scratch fever associated with an osteolytic lesion. N Engl J Med 260: 278–280, 1959.
Margileth AM, Wear DJ, English CK: Systemic cat scratch disease: Report of 23 patients with prolonged or recurrent severe bacterial infection. J Infect Dis 155: 390–402, 1987.
Rizkallah MF, Meyer L, Ayour EM: Hepatic and splenic abscesses in cat-scratch disease. Pediatr Infect Dis 7: 191–195, 1986.
Case records of the Massachusetts General Hospital. Case 22–1992. NEJM 326: 1480–1489, 1992.
Bogue CW, Wise JD, Gray GF, Edwards KM: Antibiotic therapy for Cat-scratch disease? JAMA 262: 813–816, 1989.
Holley HP Jr.: Successful treatment of Cat-scratch disease with ciprofloxacin. JAMA 265: 1563–1565, 1991.
Nelson JD: The bacterial etiology and antibiotic management of septic arthritis in infants and children. Pediatrics 50: 437–440, 1972.
Goldenberg DL, Cohen AS: Acute infectious arthritis Am J Med 60: 369–377, 1976.
Barton LL, Dunkie LM, Habib FH: Septic arthritis in childhood: A 13 year review, Am J Dis Child 141: 898–900, 1987.
Chusid MJ, Jacobs WM, Sty JR: Pseudomonas arthritis following puncture wounds of the foot. J Pediatr 94: 429–431, 1979.
Nelson JD, Howard JB, Shelton S: Oral antibiotic therapy for skeletal infections of children. I. Antibiotic concentrations in suppurative synovial fluid. J Pediatr 92: 131–134, 1978.
Bryson YJ, Connor JD, LeClere M, et al.: High-dose oral dicloxacillin treatment of acute staphylococcal osteomyelitis in children. J Pediatr 94: 673–675, 1979.
Jafari h, Friedland I, Ehrett S et al. Effects of dexamethasone and anti-CD18 antibodies on H. Inftuenzae Type B induced joint destruction. Pediatr Res 31 (#4, Pt.2): 165A, 1992.
Rush PJ, Shore A, Inman R, et al.: Arthritis associated with Haemophilus influenzae meningitis: Septic or Reactive? J Pediatr 109: 412–415, 1986.
Likitnukui S, McCracken GH, Nelson JD: Arthritis in children with bacterial meningitis. Am J Dis Child 140: 424–427, 1986.
Goldenberg DL: Infectious arthritis complicating rheumatoid arthritis and other chronic rheumatic disorders. Arthritis Rheum 32: 4596–4502, 1989.
Britigan BE, Cohen MS, Sparling PF: Gonococcal infection: A model of molecular pathogenesis. N EngJ Med 312: 1683–1694, 1985.
Hook EW III, Holmes KK: Gonococcal infections. Ann Intern Med 102: 229243, 1985.
Kerr JM, LeBlanc W, Heagarty MC: Genitourinary Gonorrhea Presenting as Mild Arthritis. Clin Pediatr 30: 388–389, 1991.
Leibel RL, Fangman JJ, Ostrovsky MC: Chronic meningococcemia in childhood. Am J Dis Child 127: 94–98, 1974.
Rosen MS, Myers AR, Dickey B: Meningococcemia presenting as septic arthritis, pericarditis, and tenosynovitis. Arthritis Rheum 28: 576–578, 1985.
Schaad UB: Arthritis in disease due to Neisseria meningitidis. Rev Infect Dis 2: 880–887, 1980.
Reginato AJ, Ferreiro JL, O’Connor CR, et al.: Clinical and pathologic studies of twenty-six patients with penetrating foreign body injury to the joints, bursae, and tendon sheaths. Arthritis Rheum 33: 1753–1762, 1990.
Kelly JJ: Blackthorn inflammation. J Bone Joint Surg 48B: 474–477, 1966.
Sugarman M, Stobie DG, Quismorio FP, et al.: Plant thorn synovitis. Arthritis Rheum 20: 1125–1128, 1977.
Barton LL, Saied KR: Thorn-induced arthritis. J Pediatr 93: 322–323, 1978.
Kleiman MB, Elfenbein DS, Wolf EL, et al.: Periosteal reaction due to foreign body induced inflammation of soft tissue. Pediatrics 60: 638–641, 1978.
Swischuk LE, Jorgenson F, Jorgenson A, et al.: Wooden splinter induced “pseudotumors” and “osteomyelitis-like lesions” of bone and soft tissues. Am J Roentgenol Radium Ther Nucl Med 122: 176–179, 1974.
O’Connor CR, Reginato AJ, Delong WG: Foreign body reactions simulating acute septic arthritis. J Rheumatol 15: 1568–1571, 1988.
Cuellar ML, Silveira LH, Espinoza LR: Fungal arthritis. Ann Rheum Dis 51: 690–697, 1992.
Bayer AS, Choi C, Tillman D, et al.: Fungal arthritis I: Candida. Semin Arthritis Rheum 8:142–150, 1978 (see also 8:200–211; 9:66–74, 145–151; 10: 218–227 ).
Katzenstein D: Isolated Candidia arthritis: report of a case and definition of a distinct clinical syndrome. Arthritis Rheum 28: 1421–1424, 1985.
Rosenthal J, Brandt KD, Wheat LJ, Slama TG: Rheumatologic manifestations of histoplasmosis in the recent Indianapolis epidemic. Arthritis Rheum 26: 1065–1070, 1983.
Kafka JA, Catanzaro A: Disseminated coccidiodomycosis in children. J Pediatr 98: 355–361, 1981.
Bocanegra T, Espinoza LR, Bridgeford P et al.: Reactive arthritis induced by parasitic infection. Ann Int Med 94: 207–209, 1981.
Zaki MH: Selected tickborne infections: A review of Lyme disease, Rocky Mountain spotted fever, and babesiosis. NYS J Med 89: 320–335 1989.
Krause PJ, Telford SR III, Pollack RJ, et al. Babesiosis: An underdiagnosed disease of children. Pediatrics 89: 1045–1948, 1992.
Gunasekaran TS, Hassall E: Giardiasis mimicking inflammatory bowel disease. J Pediatr 120: 424–426, 1992.
Lakhanpal S, Cohen SB, Fleischmann RM: Reactive arthritis from Blastocystis hominis. Arthritis Rheum 34: 251–253, 1991.
Shaw RA, Stevens MB: The reactive arthritis of giardiasis: A case Report, JAMA 258: 2734–2735, 1987.
Borella L, Goobar JE, Clark GM: Synovitis of the knee joints in late congenital syphilis. JAMA 180: 190–192, 1962.
Chapel TA: Physician recognition of the signs and symptoms of secondary syphilis. JAMA 246: 250–251, 1981.
Reginato AJ, Schumacher HR, Jiminez S, et al.: Synovitis in secondary syphilis. Arthritis Rheum 22: 170–176, 1979.
Gould K: Clinical recognition of leptospirosis. Intern Med 2: 51–58, 1981.
Raffin BJ, Freemark M: Streptobacillary rat-bite fever: A pediatric problem. Pediatrics 64: 214–217, 1979.
Shanson DC, Gazzard BG, Midgley J, et al. Streptobaccilus moniliformis isolated from blood in four cases of Haverhill Fever. Lancet 2: 92–94, 1983.
Madden, M: Polyarthritis due to rate bite fever. IM: 16–19, 1991.
Gordon SC, Lauter CB: Mumps arthritis: unusual presentation as adult Still’s disease. Ann Intern Med 97: 45–47, 1982.
Cwajgenbaum M, Azem I, Weisbrod M, et al.: Arthritis in chickenpox. Am J Dis Child 140: 502, 1986.
Roberts-Thomson PJ, Ahern MJ, Southwood TR, et al.: Adult onset Still’s disease or Coxsackie polyarthritis? Aust NZ J Med 16: 509–511, 1986.
Hawkes RA, Boughton CR, Naim HM, Stallman ND: A major outbreak of epidemic polyarthritis in New South Wales during the summer of 1983/1984. Med J Aust 143: 330–333, 1985.
Remafedi G, Muldoon RL: Acute monarticular arthritis caused by Herpes Simplex Virus Type 1. Pediatrics 72: 882–883, 1983.
Sigal LH, Steere AC, Niederman JC: Symmetric polyarthritis associated with heterophile-negative infectious mononucleosis. Arthritis Rheum 26: 553–556, 1983.
Ray CG, Gall EP, Minnich LL, et al.: Acute polyarthritis associated with active Epstein-Barr virus infection. JAMA 248: 2990–2994, 1982.
Marshall GS, Starr SE, Witzleben CL, et al.: Protracted mononucleosis-like illness associated with acquired cytomegalovirus infection in a previously healthy child: Transient cellular immune defects and chronic hepatopathy. Pediatrics 87: 556–562, 1991.
Petty RE, Tingle AJ: Arthritis and viral infection. J Pediatr 113: 948–949, 1985.
Phillips PE: Evidence implicating infectious agents in rheumatoid arthritis and juvenile rheumatoid arthritis. Clin Exp Rheumatol 6: 87–94, 1988.
Vaughan JH: Infection and Rheumatic Diseases: A Review. Bulletin on the Rheumatic Diseases 39: #1 2, 1990; Arthritis Foundation.
Chantler JK, Tingle AJ, Petty RE: Persistant rubella virus infection associated with chronic arthritis in children. N Eng J Med 313: 1117–1123, 1985.
Niklasson B, Espmark A: Ockelbo disease: Arthralgia 3–4 years after infection with a sindbis virus related agent. Lancet 1: 1039–1040, 1986.
FraserJRE, Cunningham AL, Hayes K, et al.: Rubella arthritis in adults. Isolation of virus, cytology and other aspects of the synovial reaction. Clin Exp Rheumatol 1: 287–293, 1983.
Spruance SL, Metcalf R, Smith CB, et al.: Chronic arthropathy associated with rubella vaccination. Arthritis Rheum 20: 741–747, 1977.
Jacobs, JC: Childhood arthritis following rubella booster immunizations: Is arthritis more frequent in immune individuals? Pediatr Res. 29 (#4.Pt2): 175A, 1991.
Utsinger PD: Immunopathogenesis of chronic post-rubella vaccination arthritis. Arthritis Rheum 22: 667–668, 1979.
Grahame R, Armstrong R, Simmons N, et al.: Chronic arthritis associated with the presence of intrasynovial rubella virus. Ann Rheum Dis 42: 2–13, 1983.
Wands JR, Mann E, Alpert E, et al.: The pathogenesis of arthritis associated with acute hepatitis-B surface antigen-positive hepatitis. Complement activation and characterization of circulating immune complexes. J Clin Invest 55: 930–936, 1975.
Perrillo RP, Pohl DA, Roodman ST, et al.: Acute non-A, non-B hepatitis with serum-sickness-like syndrome and aplastic anemia. JAMA 245: 494–496, 1981.
Dan M, Yaniv R: Cholestatic hepatitis, cutaneous vasculitis, and vascular deposits of immunoglobulin M and complement associated with hepatitis A virus infection. Am J Med 89: 103–104, 1990.
Woolf AD, Campion GV, Chishick A, et al.: Clinical manifestation of human parvovirus B19 in adults. Arch Intern Med 149: 1153–1156, 1989.
Naides SJ, Scharosch LL, Foto F, Howard EJ: Rheumatologic manifestations of human parvovirus B19 infection in adults. Initial two-year clinical experience. Arthritis Rheum 33: 1297–1309, 1990.
NoctonJJ, Miller LC, Tucker LB, Schaller JG. Human parvovirus B19 arthritis in children. Pediatr Res 31 (#4,Pt.2): 172A, 1992.
Bruchoff SE, Woda BA, Pihan GA, et al.: Parvovirus B 19-Associated hemophagocytic syndrome. Arch Intern Med 150: 897–899, 1990.
Dinerman JL, Corman LC: Human parvovirus B19 arthropathy associated with desquamation. Am J Med 89: 826–828, 1990.
Finkel TH, Gelfand EW, Harbeck R, et al.: Chronic parvovirus infection presenting as juvenile polyarteritis nodosum. Arthritis Rheum 33: 5132, 1990.
Kaplan MM: The spectrum of chronic active liver disease. Hosp Practice pp. 67–75, October 1983.
Vergani D, Larcher VF, Davies ET, et al.: Genetically determined low C4: a predisposing factor to autoimmune chronic active hepatitis. Lancet 2: 294–297, 1985.
Fitz JG, Petri M, Hellmann D: Chronic active hepatitis presenting with rheumatoid nodules and arthritis. J Rheumatol 14: 595–598, 1987.
Maggiore G, Porta G, Bernard O, et al.: Autoimmune hepatitis with initial presentation as acute hepatic failure in young children. J Pediatr 116: 280–282, 1990.
Ponka A: Arthritis associated with Mycoplasma pneumoniae infection. Scand J Rheum 8: 27–32, 1979.
Davis CP, Cochran S, Lisse J, et al.: Isolation of Mycoplasma pneumoniae from synovial fluid samples in a patient with pneumonia and polyarthritis. Arch Intern Med 148: 969–970, 1988.
Bhopal RS, Thomas GO: Psittacosis presenting with Reiter’s syndrome. Br Med J 284: 1606, 1982.
Helmick CG, Bernard KW, D’Angelo LJ: Rocky Mountain spotted fever: Clinical, laboratory, and epidemiological features of 262 cases. J Infect Dis 150: 480–488, 1984.
Massarotti EM, Luger SW, Rahn DW et al. Treatment of early Lyme disease. Am J Med 92: 396–403, 1992.
Steere AC: Lyme disease. N Eng J Med 321: 566–596, 1989.
White DJ, Chang Hwa-Gan, Benach JL, et al.: The geographic spread and temporal increase of the Lyme disease epidemic. JAMA 266: 1230–1236, 1991.
Alpert B, Esin J, Sivak SL, Wormser GP: Incidence and prevalence of Lyme Disease in a suburban Westchester County community. NYS J Med 92:5–8, 1992. ( See also: Editorial pp 2–4 )
Williams CL, Strobino B, Lee A, et al.: Lyme disease in childhood: clinical epidemiologic features of ninety cases. Pediatr Infect Dis J 9: 10–14, 1990.
Eichenfield AH, Goldsmith DP, Benach JL, et al.: Childhood Lyme arthritis in an endemic area. J Pediatr 109: 753–758, 1986.
Benach JL, Bosler EM: Lyme disease and related disorders. Ann NY Acad Sci 539: 1–150, 1988.
Piesman J, Mather TN, Sinskey RJ, Spielman A: Duration of tick attachment and Borrelia burgdorferi transmission. J Clin Microbiol 25: 557–558, 1987.
Nadelman RB, Pavia CS, Magnarelli LA, Wormser GP: Isolation of Borrella burgdorferi from the blood of seven patients with Lyme disease. Am J Med 88: 21–26, 1990.
Johnston YE, Duray PH, Steere AC, et al.: Lyme arthrtis: Spirochetes found in synovial microangiopathic lesions. Am J Pathol 118: 26–34, 1985.
Jacobs JC, Stevens M, Duray PH: Lyme disease simulating septic arthritis. JAMA 256: 1138–1139, 1986.
Kay J, Eichenfield AH, Atheya BH, et al.: Synovial fluid eosinophilia in Lyme disease. Arthritis Rheum 31: 1384–1389, 1988.
Farris BK, Webb RM: Lyme disease and optic neuritis. J Clin Neuroophthalmol 8: 73–78, 1988.
Meier C, Grahmann F, Englehardt, Dumas M: Peripheral nerve disorders in Lyme-Borreliosis: Nerve biopsy studies from eight cases. Acta Neuropathol 79: 271–278, 1989.
May EF, Jabbari B: Stroke in Neuroborreliosis. Stroke 21: 1232–1235, 1990.
Pachner AR, Duray P, Steere AC: Central nervous system manifestations of Lyme disease. Arch Neurol 46: 790–795, 1989.
Feder HM, Zalneraitis EL, Reik L Jr: Lyme disease: acute focal meningoencephalitis in a child. Pediatrics 82: 931–934, 1988.
Luft BJ, Steinman CR, Neimark HC et al. Invasion of the central nervous system by borrelia burgdorferi in acute disseminated infection. JAMA 267: 1364–1367, 1992.
Logigian EL, Kaplan RF, Steere AC: Chronic neurologic manifestations of Lyme disease. N Eng J Med 323: 1438–1444, 1990.
Jacobs JC, Rosen JM, Szer IS: Lyme myocarditis diagnosed by gallium scan. J Pediatr 105: 950–952, 1984.
Rienzo RJ, Morel DE, Prager D, et al.: Gallium avid Lyme myocarditis. Clin Nucl Med 12: 475–476, 1987.
Olson LJ, Okafor EC, Clements IP: Cardiac involvement in Lyme disease: Manifestations and management. Mayo Clin Proc 61: 745–749, 1986.
Marcus LC, Steere AC, Duray PH, et al.: Fatal pancarditis in a patient with coexistent Lyme disease and babesiosis: demonstration of spirochetes in the myocardium. Ann Intern Med 103: 374–376, 1985.
Reznick JW, Braunstein DB, Walsh RL, et al.: Lyme carditis: electrophysiologic and histopathologic study. Am J Med 81: 923–927, 1986.
Stanek G, Klein J, Bittner R, Glogar D: Isolation of Borrelia burgdorferi from the mycardium of a patient with longstanding cardiomyopathy. N Eng J Med 322: 249–252, 1990.
Kishaba RG, Weinhouse E, Chusid MJ, Nudel DB: Lyme disease presenting as heart block. Clin Pediatr 27: 291–293, 1988.
McAlister HF, Klementowicz PT, Andrews C, et al.: Lyme carditis: an important cause of reversible heart block. Ann Intern Med 110: 339–345, 1989.
van der Linde MR, Crijns JGM, de Koning J, et al.: Range of atrioventricular conduction distrubances in Lyme borreliosis: A report of four cases and review of other published reports. Br Heart J 63: 162–168, 1990.
Kimball SA, Janson PA, LaRaia PJ: Complete heart block as the sole presentation of Lyme disease. Arch Intern Med 149: 1897–1898, 1989.
Baylac-Domengetroy F, Vieyres C, Barraine R: Complete heart block as the sole presentation of Lyme disease. Arch Intern Med 151: 1240, 1991.
Artigao R, Torres G, Guerrero A, et al.: Irreversible complete heart block in Lyme disease. Am J Med 90: 531–533, 1991.
Atlas E, Novak SN, Duray PH, Steere AC: Lyme myositis: muscle invasion by Borrelia burgdorferi. Ann Intern Med 103: 245–246, 1988.
Reimers CD, Pongratz DE, Neubert U, et al.: Myositis caused by Borrelia burgdorferi: report of four cases. J Neurol Sci 91: 215–226, 1989.
Szer IS, Taylor E, Steere AC: The clinical course and long-term follow-up of children with lyme arthritis. N Eng J Med 325: 159–163, 1991.
Logigian EL, Kaplan RF, Steere AC: Chronic neurologic manifestations of Lyme disease. N Eng J Med 323: 1438–1444, 1990.
Arnett FC: The Lyme spirochete: another cause of Reiter’s syndrome? Arthritis Rheum 32: 1182–1184, 1989.
Kaell AT, Volkman DJ, Gorevic PD, Dattwyler RJ: Positive Lyme serology in subacute bacterial endocarditis. A study of four patients. JAMA 2916–2918, 1990.
Feder HM Jr, Shapiro ED, Gerber MA, Hunt M: Common problems in the diagnosis and management of Lyme disease. Pediatr Res 31 (#4,Pt.2): 122A, 1992.
Gerber MA, Shapiro ED: Diagnosis of Lyme disease in children. J Pediatr 121: 157–162, 1992.
Schutzer SS, Coyle PK, Belman AL, et al.: Sequestration of antibody to Borrelia burgdorferi in immune complexes in serongegative Lyme disease. Lancet 1: 312–315, 1990.
Hardin JA, Steere AC, Malawista SE: Immune complexes and the evolution of Lyme arthritis N Engl J Med 301: 1358–1363, 1979.
Hedberg CW, Osterholm MT: Serologic tests for antibody to Borrelia burgdorferi: Another Pandora’s box for medicine? Arch Intern Med 150: 732–733, 1990.
Rose CD, Fawcett PT, Singsen BH, et al.: Use of western blot and enzyme-linked immunosorbent assays to assist in the diagnosis of lyme disease. Pediatrics 33: 465–70, 1991.
Krause A, Brade V, Schoerner C, et al.: T cell proliferation induced by Borrelia burgdorferi in patients with Lyme borreliosis. Arthritis Rheum 34: 393–402, 1991.
Salazar J, Gerber M, Goff C. Long-term outcome of children with early Lyme disease. Pediatr Res 31 (#4,Pt.2): 178A, 1992.
Rahn DW, Malawista SE: Clinical judgment in Lyme disease. Hospital Practice pp. 39–56, March 30, 1990.
Sigal LH: Summary of the first 100 patients seen at a Lyme disease referral center. Am J Med 88: 577–581, 1990.
Cooper JD, Schoen RT: Epidemiology, clinical features, and diagnosis of Lyme disease. Curr Opin Rheum 4: 520–528, 1992.
Wrenn K: Ceftriazone versus cefuroxime for meningitis in children. N Eng J Med 322: 1821, 1990.
Snydman DR, Schenkein DP, Berardi VP, et al.: Borrelia burgdorferi in joint fluid in chronic lyme arthritis. Ann Intern Med 104: 798–800, 1986.
Schoen RT, Aversa JM, Rahn DW, Steere AC: Treatment of refractory chronic lyme arthritis with arthroscopic synovectomy. Arthritis Rheum 34: 1056–60, 1991.
Steere AC, Dwyer E, Winchester R: Association of chronic Lyme arthritis with HLA-DR2 alleles. N Eng J Med 323: 219–223, 1990.
Yoshinari NH, Reinhardt BN, Steere AC: T cell responses to polypeptide Fractions of Borrelia burgdorferi in patients with Lyme arthritis. Arthritis Rheum 34: 707–713, 1991.
Schlesinger PA, Burke BA, Stillman T: Maternal-fetal transmission of the Lyme disease spirochete, Borrelia burgdorferi. Ann Intern Med 103: 67–68, 1985.
MacDonald AB, Benach JL, Burgodorfer W: Stillbirth following maternal Lyme disease. NYS J Med 87: 615–616, 1987.
Levo Y, Nashif M: Musculosekeletal manifestations of bacterial endocarditis. Clin Exp Rheumatol 1: 49–52, 1983.
Pinals RS, Tunnessen WW: Shunt arthritis. J Pediatr 91: 681, 1977.
ter Bory EJ, Van Rijswijk MH, Kallenberg CGM: Transient arthritis with positive tests for rheumatoid factor as presenting sign of shunt nephritis. Ann Rheum Dis 50: 182–183, 1991.
Knitzer PH, Needleman BW: Musculoskeletal syndromes associated with acne. Semin Arthritis Rheum 20: 247–255, 1991.
Rosner IA, Richter DE, Huettner TL, et al.: Spondyloarthropathy associated with hidradenitis suppurative and acne conglobata. Annals Intern Med 97: 520525, 1982.
Wands JR, Lamont JT, Mann E, et al.: Arthritis associated with intestinal bypass procedure for morbid obesity. N Engl J Med 294: 121–124, 1976.
Utsinger PD: Bypass disease: A bacterial antigen-antibody systemic immune complex disease. Arthritis Rheum 23: 758, 1980.
Jorizzo JL, Apisarnthanarax P, Subrt P, et al.: Bowel-bypass syndrome without bowel bypass. Arch Intern Med 143: 457–461, 1983.
LeVine ME, Dobbins WO III: Joint changes in Whipple’s disease. Semin Arthritis Rheum 3: 79–93, 1973.
Fleming JL, Wiesner RH, Shorter RG: Whipple’s disease: Clinical, biochemical and histopathologic features and assessment of treatment in 29 patients. Mayo Clin Proc 63: 539–551, 1988.
Southern JF, Moscicki RA, Magro C, et al.: Lymphedema, lymphocytic myocarditis, and sarcoidlike granulomatosis: Manifestations of Whipple’s disease. JAMA 261: 1467–1470, 1989.
MacCarthy J, O’Brien N: Phalangeal microgeodic syndrome of infancy. Arch Dis Child 51: 472–474, 1976.
Kaibara N, Masuda S, Katsuki I, et al.: Phalangeal microgeodic syndrome in childhood: report of seven cases and review of the literature. Eur J Pediatr 136: 41–46, 1981.
Winchester R: AIDS and the rheumatic diseases. Bull Rheum Dis (Arthritis Foundation) Vol. 39, No. 5, pp. 1–10, 1990.
Nordstrom DM, Petropolis AA, Giorno R, et al.: Inflammatory myopathy and acquired immunodeficiency syndrome. Arthritis Rheum 32:475–479, 1989 (see also correspondence 33: 298, 1990 ).
Walter EB, Drucker RP, McKinney RE, Wilfert CM: Myopathy in human immunodeficiency virus-infected children receiving long-term Zidovudine therapy. J Pediatr 119: 152–155, 1991.
D’Agati V, Seigle R: Coexistence of AIDS and lupus nephritis: a case report. Am J Nephrol 10: 243–247, 1990.
Sculerati N, Borkowsky W: Pediatric human immunodeficiency virus infection: an otolaryngologist’s perspective. J Otolaryngol 19: 182–188, 1990.
Soberman N, Leonidas JC, Berdon WE, et al.: Sonographic observations of parotid enlargement in 10 HIV positive children. AJR 157: 553–556, 1991.
Yancey WB Jr, Dolson LH, Oblon D, et al.: HTLV-1-associated adult T-cell leukemia/lymphoma presenting with nodular synovial masses. Am J Med 89: 676–683, 1990.
Lohr KM: Rheumatic manifestations of diseases associated with substance abuse. Semin Arthritis Rheum 17: 90–111, 1987.
Kaye BR, Fainstat M: Cerebral vasculitis associated with Cocaine abuse. JAMA 258: 2104–2106, 1987.
Daggett RB, Haghighi P, Terkeltaub RA: Nasal cocaine abuse causing an aggressive midline intranasal and pharyngeal destructive process mimicking midline reticulosis and limited Wegener’s Granulomatosis. J Rheumatol 17: 838–840, 1990.
b.Lam M, Ballou SP. Reversible scleroderma renal crisis after cocaine use. NEJM 326: 1435, 1992.
Haueisen DC, Weiner DS, Weiner SD: The characterization of “transient synovitis of the hip” in children. J Pediatr Orthop 6: 11–17, 1986.
Bickerstaff DR, Neal LM, Brennan PO, Bell MJ: An investigation into etiology of irritable hip. Clin Pediatr 30: 353–356, 1991.
Lindsley CB. SchallerJG: Arthritis associated with inflammatory bowel disease in children. J Pediatr 84: 16–20, 1974.
Burbige EJ, Huang SS, Bayless TM: Clinical manifestations of Crohn’s disease in children and adolescents. Pediatrics 55: 866–871, 1975.
Passo MH, Fitzgerald JF, Brandt KD: Arthritis associated with inflammatory bowel disease. Dig Dis Cl 31: 492–497, 1986.
Orholm M, Munkholm P, Langholz E, et al.: Familial occurrence of inflammatory bowel disease. N Eng J Med 324: 84–88, 1991.
Heyman MB, Perman JA, Ferrell LD, Thaler MM: Chronic nonspecific inflammatory bowel disease of the cecum and proximal colon in children with grossly normal-appearing colonic mucosa: diagnosis by colonoscopic biopsies. Pediatrics 80: 255–261, 1987.
Al-Hadidi, Khatib G, Chhatwal P, Khatib R: Granulomatous arthritis in Crohn’s disease. Arthritis Rheum 27: 1061–1062, 1984.
Dyer NH, Dawson AM, Verbov JL., et al.: Cutaneous polyarteritis nodosa associated with Crohn’s disease. Lancet 1: 648–650, 1970.
Thompson DG, Lennard-Jones JE, Swarbrick ET, et al.: Pericarditis and inflammatory bowel disease. Q J Med 189: 93–97, 1979.
Dawes PT, Atherton ST: Coeliac disease presenting as recurrent pericarditis. Lancet 1: 1021–1022, 1981.
Sohar E, Gafni J, Pras M, Heller H: Familial Mediterranean fever. Am J Med 43: 227–253, 1967.
Lehman TJA, Peters RS, Hanson V, Schwabe AD: Long-term colchicine therapy of familial Mediterranean fever. J Pediatr 93: 876–878, 1978.
Majeed HA, Carroll JE, Khuffash FA, Hijazi Z: Long-term colchicine prophylaxis in children with familial Mediterranean fever (recurrent hereditary polyserositis). J Pediatr 116: 997–999, 1990.
Matzner Y, Ayesh SK, Hochner-Celniker D, et al.: Proposed mechanism of the inflammatory attacks in familial Mediterranean fever. Arch Intern Med 150: 1289–1291, 1990.
Ozyilkan E, Simsek H, Telatar H. Tumor necrosis factor in familial Mediterranean fever. Am J Med 92: 579–580, 1992.
Pras E, Aksentijevich I, Gruberg L, et al. Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. NEJM 326: 1509 1513, 1992.
Majeed HA, Baraket M: Familial Mediterranean fever (recurrent hereditary polyserositis) in children: analysis of 88 cases. Eur J Pediatr 148: 636–641, 1989.
Zemer D, Pras M, Sohar E, et al.: Colchicine in the prevention and treatment of the amyloidosis of familial Mediterreanean fever. N Eng J Med 314: 1001–1005, 1986.
Schwabe AD, Monroe JB: Meningitis in familial Mediterranean fever. Am J Med 85: 715–717, 1988.
Majeed HA, Quabazard Z, Hijazi Z, et al.: The Cutaneous manifestations in children with familial Mediterranean fever (Recurrent hereditary polyserositis). A six-year study. Q J Med 278: 607–616, 1990.
Heller H, Gafni J, Michaeli D, et al.: The arthritis of familial Mediterranean fever. Arthritis Rheum 9: 1–17, 1966.
Simon G, Marbach JJ: Familial Mediterranean fever with temporomandibular joint arthritis. Pediatrics 57: 801–812, 1976.
Lehman TJA, Hanson V, Kornreich H, et al.: HLA-B27 negative sacroilitis: A manifestation of familial Mediterranean fever in childhood. Pediatrics 61: 423426, 1978.
Cohen AS: Amyloidosis. Bull Rheum Dis (Arthritis Foundation) 40: No. 2 pp. 1–12, 1991.
Bakir F, Murtadha M, Issa N: Amyloidosis and periodic peritonitis (familial Mediterranean fever). West J Med 131: 193–195, 1979.
Pras M, Gafni J, Jacob ET, et al.: Recent advances in familial Mediterranean fever. In Yearbook of Medicine. Year Book Medical Publishers, pp. 261–270, 1984.
Wallace SL: Colchicine. Semin Arthritis Rheum 3: 369–381, 1974.
Kund RW, Duncan G, Watson D, et al. Colchicine myopathy and neuropathy. N Engl J Med 316: 1562–1568, 1987.
Chang Yi Han: Mechanism of action of colchicine. Arthritis Rheum 18: 493496, 1975.
Kilburn HL: Solitary mastocytoma of infancy. Clin Pediatr 13: 60–62, 1974.
Marshall J, Walker J, Lurie HI, et al.: Solitary mastocytoma and the mastocytoses. S Afr Med J 31: 867–876, 1957.
Demis DJ: The mastocytosis syndrome: Clinical and biological studies. Ann Intern Med 59: 194–206, 1963.
Lindsley CB, Miner PB Jr: Seronegativejuvenile rheumatoid arthritis and mast cell-associated gastritis. Arthritis Rheum 34: 106–109, 1991.
Melamed I, Feanny SJ, Sherman PM, Roifman CM: Benefit of Ketotifen in patients with eosinophilic gastroenteritis. Am J Med 90: 310–314, 1991.
McAdam LP, O’Hanlan MA, Bluestone R, Pearson CM: Relapsing polychondritis. Medicine 55: 193–215, 1976.
Isaak BL, Liesegang TJ, Michet CJ: Ocular and systemic findings in relapsing polychondritis. Ophthalmology 93: 681–689, 1986.
O’Hanlon M, McAdam LP, Bluestone R, Pearson CM: The arthropathy of relapsing polychondritis. Arthritis Rheum 19: 191–194, 1976.
Hashimoto K, Arkin CR, Kang HA: Relapsing polychondritis: An ultrastructural study. Arthritis Rheum 20: 91–97, 1977.
Arundell FW, HaserickJR: Familial chronic atrophic polychondritis. Arch Dermatol 82: 439–440, 1960.
Blau EB: Relapsing polychondritis and retropertioneal fibrosis in an 8-year-old boy. Am J Dis Child 130: 1149–1152, 1976.
Muckle TJ: The `Muckle-Wells’ syndrome. J Dermatol 100: 87–92, 1979.
Darranco VP, Minor DB, Solomon H: Treatment of relapsing polychondritis with dapsone. Arch Dermatol 112: 1286–1288, 1976.
Bowness P, Hawley IC, Morris T, et al.: Complete heart block and severe aortic incompetence in relapsing polychondritis: clinicopathologic findings. Arthritis Rheum 34: 97–100, 1991.
Goldbloom RB, Stein PB, Eisen A, et al.: Idiopathic periosteal hyperostosis with dysproteinemia. A new clinical entity. N Engl J Med 274:873–878, 1966 (see also Goldbloom RB: Commentary. In: Gellis SS (ed.) Yearbook of Prediatrics, Yearbook Medical Pub., Chicago, 1977, p. 308 ).
Cameron BJ, Laxer RM, Wilmot DM, et al.: Idiopathic periosteal hyperostosis with dysproteinema (Goldbloom’s syndrome): case report and review of the literature. Arthritis Rheum 30: 1307–1312, 1987.
Goldsmith DP, Rose CD, Sharrar WC, et al.: Idiopathic multifocal periostitis (IMP)—a rare entity simulating JRA. Arthritis Rheum 33: S89, 1990.
Gerscovich EO, Greenspan A, Lehman WB: Idiopathic periosteal hyperostosis with dysproteinemia-Goldbloom’s syndrome. Pediatr Radiol 20: 208–211, 1990.
Ringel RE, Haney PJ, Brenner JI, et al.: Periosteal changes secondary to prostaglandin administration. J Pediatr 103: 251–253, 1983.
Dupont AG, Verbeelen DL, Six RO: Weber-Christian panniculitis with mem-branous glomerulonephritis. Am J Med 75: 527–528, 1983.
Case records of the Massachusetts General Hospital. Case 21–1984. N Eng J Med 310: 1374–1381, 1984.
Sorenson RU, Abramowsky CR, Stern RC: Ten-year course of early-onset Weber-Christian syndrome with recurrent pneumonia: a suggestion for pathogenesis. Pediatrics 78: 115–120, 1986.
Lemley DE, Chun B, Cupps TR: Sterile splenic abscesses in systemic Weber-Christian disease. Unique source of abdominal pain. Am J Med 83: 567–570, 1987.
Buck BE, Yang LC, Caleb MH, et al.: Measles virus panniculitis subsequent to vaccine administration. J Pediatr 101: 366–373, 1982.
Ilowite, N. Personal Communication.
Marhaug G, Havidsten D: Arthritis complicating acute pancreatitis—a rare but important condition to be distinguished from juvenile rheumatoid arthritis. Scand J Rheumatol 17: 397–399, 1988.
Jakobiec FA, Mottow L: Pediatric orbital pseudotumor. In: Jakobiec FA (ed.) Ocular and Adnexal Tumors. Aesculapius Press, Birmingham, AL, 1978, pp. 644–658.
Saul RA, Lee WH, Stevenson RE: Caffey’s disease revisited: further evidence for autosomal dominant inheritance with incomplete penetrance. Am J Dis Child 136: 56–60, 1982.
Heyman E, Laver J, Beer S: Prostaglandin synthetase inhibitor in Gaffey disease. (Letter) J Pediatr 101: 314, 1982.
Parker S, Griffiths HJ: Prostaglandin induced cortical hyperostosis. Orthopedics 13: 243–244, 1990.
Younge D, Drummond D, Herring J, Cruess RL: Melorheostosis in children: clinical features and natural history. J Bone Joint Surg 61-B: 415, 1979.
Dimar JR, Campion TS: Melorheostosis: Two case presentations and review of the literature. Orthop Rev 16: 615–621, 1987.
Abdul-Karim FW, Carter JR, Makley JT, et al.: Intramedullary osteosclerosis. A report of the clinicopathologic features a five cases. Orthopedics 11: 1667 1676, 1988.
Furia JP, Schwartz HS: Hereditary multiple diaphyseal sclerosis: A tumor simulator. Orthopedics 13: 1267–1274, 1990.
Hoover DL, Khan JA, Giangiacomo J: Pediatric ocular sarcoidosis. Sury Ophthalmol 30: 215–228, 1986.
Pattishall EN, Strope GL, Spinola SM, Denny FW: Childhood sarcoidosis. J Pediatr 108: 169–177, 1986.
Lindsley CB, Godfrey WA: Childhood sarcoidosis manifesting as juvenile rheumatoid arthritis. Pediatrics 76: 765–768, 1985.
Sahn EE, Hampton MT, Garen PD, et al.: Preschool sarcoidosis masquerading as juvenile rheumatoid arthritis: Two case reports and a review of the literature. Pediatr Dermatol 7: 208–13, 1990.
Gross KR, Malleson PN, Culham G, et al.: Vasculopathy with renal artery stenosis in a child with sarcoidosis. J Pediatr 109: 387, 1986.
Jabs DA, Houk JL, Bias WB, Arnett FC: Familial granulomatous synovitis, uveitis, and cranial neuropathies. Am J Med 78: 801–804, 1985.
Miller JJ: Early-onset “sarcoidosis” and “familial granulomatous arthritis (arteritis)”: The same disease. J Pediatr 109: 387, 1986.
Pastores GM, Michels VV, Stickler GB, et al.: Autosomal dominant granulomatous arthritis, uveitis, skin rash, and synovial cysts. J Pediatr 117: 403–408, 1990.
Rose CD, Eichenfield AH, Goldsmith DP, Athreya BH: Early onset sarcoidosis with aortitis—“juvenile systemic granulomatosis? ” J Rheumatol 17: 102–106, 1990.
Shaikh S, Soubani AO, Rumore P et al.: Lytic osseous destruction in vertebral sarcoidosis. NYS J Med 92:213–218, 1992 (Also see Editorial, pp. 177–178).
Simons FER, Schaller JG: Benign rheumatoid nodules. Pediatrics 56: 29–33, 1975.
Rao NA, Font RL: Pseudorheumatoid nodules of the ocular adnexa. Am J Ophthalmol 79: 471–478, 1975.
Knigh PJ, Reiner CB: Superficial lumps in children. Pediatrics 72: 147–153, 1983.
Rush PJ, Bernstein BH, Smith CR, Shore A: Chronic arthritis following benign rheumatoid nodules of childhood. Arthritis Rheum 28: 1175–1178, 1985.
Kaye BR, Kaye RL, Bobrove A: Rheumatoid nodules: Review of the spectrum of associated conditions and proposal of a new classification, with a report of four seronegative cases. Am J Med 76: 279–292, 1984.
Jacobs JC: JRA and hyperphosphatasemia. J Pediatr 107: 828–829, 1985.
Schonau E, Herzog KH, Bohles HJ: Transient hyperphosphatasaemia of infancy. Eur J Pediatr 148: 264–266, 1988.
Kurzrock R, Cohen PR: Erythromelalgia: Review of clinical characteristics and pathophysiology. Am J Med 91:416–422, 1991 (See also 93: 111–114, 1992 ).
Rush PJ, Shore A, Coblentz C, Wilmot D, Corey M, Levison H: The musculoskeletal manifestations of cystic fibrosis. Semin Arthritis Rheum 15: 213–225, 1986.
Petty RE, Cassidy JT, Heyn R, et al.: Secondary hypertrophic osteoarthropathy. An unusual cause of arthritis in childhood. Arthritis Rheum 19: 902–906, 1976.
Schaller J: Arthritis as a presenting manifestation of malignancy in children. J Pediatr 81: 793–797, 1972.
Fink CW, Windmiller J, Sartain P: Arthritis as the presenting feature of childhood leukemia. Arthritis Rheum 15: 347–349, 1972.
Lopez-Enriquez E, Morales AP, Robert F: Effect of atropine sulfate in pulmonary hypertrophic osteoarthropathy. Arthritis Rheum 23: 822–824, 1980.
Sagransky DM, Greenwald JD: Seropositive rheumatoid arthritis in a patient with cystic fibrosis. Am J Dis Child 134: 318–319, 1980.
Schidlow DV, Goldsmith DP, Palmer J, Huang NN: Arthritis in cystic fibrosis. Dis Child 59: 377–379, 1984.
Dixey J, Redington AN, Butler RC, et al.: The arthropathy of cystic fibrosis. Ann Rheum Dis 47: 218–233, 1988.
Cohen AM, Yulish BS, Wasser KB, et al.: Evaluation of pulmonary hypertrophie osteoarthropathy in cystic fibrosis. Am J Dis Child 140: 74–77, 1986.
Maki M, Hallstrom O, Verronen P, et al.: Reticulin antibody, arthritis, and coeliac disease in children. Lancet 1: 479–480, 1988.
Riely CA: Familial intrahepatic cholestasis: an overview. In: Walker WA, Durk PR, Hamilton JR, et al. (eds.) Pediatric Gastrointestinal Disease. B.C. Decker, Philadelphia, 1990, pp. 1025–1332.
Baker DH, Harris RC: Congenital absence of the intrahepatic bile ducts. Am J Roent 91: 875–884, 1964.
Rogalsky RJ, Black GB, Reed MH: Orthopaedic manifestations of leukemia in children. J Bone Joint Surg 68A: 494–501, 1986.
Musiej-Nowakowska E, Rostropowicz-Denisiewicz K: Differential diagnosis of neoplastic and rheumatic diseases in children. Scand J Rheum 15: 124–128, 1986.
Berkelbach JW, Sprenkel VD, Timmermans AJM, et al.: Polyarthritis as the presenting symptom of a malignant fibrous histiocytoma of the heart. Arthritis Rheum 28: 944–947, 1985.
Jonsson OG, Sartain P, Ducore JM, Buchanan GR: Bone pain as an initial symptom of childhood acute lymphoblastic leukemia: association with nearly normal hematologic indexes. J Pediatr 117: 233–237, 1990.
Case records of the Massachusetts General Hospital: Case 14–1986. N Eng J Med 314: 973–981, 1986.
Ruzal-Shapiro C, Berdon WE, Cohen MD, Abramson SJ: MR imaging of diffuse bone marrow replacement in pediatric patients with cancer. Radiology 181: 587–589, 1991.
Boumpas DT, Wheby MS, Jaffe ES, et al.: Synovitis in angioimmunoblastic lymphadenopathy with dysproteinemia simulating rheumatoid arthritis. Arthritis Rheum 33: 578–582, 1990.
Kaiser BA, Mochon M, Chadarevian, J-P de: Eleven-year-old girl with acute renal failure, arthritis, hyperuricemia, and family history of rheumatic disorders. J Pediatr 121: 317–322, 1992.
Martinez-Lavin M, Pineda C, Valdez T, et al.: Primary hypertrophic osteoarthropathy. Semin J Arthritis Rheum 17: 156–162, 1988.
Cooper RG, Freemont AJ, Riley M, et al.: Bone abnormalities and severe arthritis in pachydermoperiostosis. Ann Rheum Dis 51: 416–419, 1992.
Rosen PR, Micheli LJ, Treves S: Early scintigraphic diagnosis of bone stress and fractures in athletic adolesecents. Pediatrics 70: 11–15, 1982.
Engh CA, Robinson RA, Milgram J: Stress fractures in children. Trauma 10: 532–541, 1970.
Devas M: Stress Fractures. Churchill Livingstone, Edinburgh, 1975.
Beals RK, Cook RD: Stress Fractures of the Anterior Tibial Diaphysis. Orthopedics 14: 869–875, 1991.
Cruess RI: The pathology of acute necrosis of cartilage in slipping of the capital femoral epiphysis. J Bone Joint Surg 45A: 1013–1024, 1963.
Bleck EE: Idiopathic chondrolysis of the hip. J Bone Joint Surg 65A: 1266–1275, 1983.
Taillard W, Grasset E: La coxite laminaire juvenile. Revue Chir Orthop 50: 159–181. 1964.
Bernstein B, Forrester D, Singsen B, King KK, Kornreich H, Hanson V: Hip joint restoration in juvenile rheumatoid arthritis. Arthritis Rheum 20: 1099 1104, 1977.
Ippolito E, Bellocci, Santori FS, Ghera S: Idiopathic chondrolysis of the hip: An ultrastructural study of the articular cartilage of the femoral head. Orthopedics 9: 1383–1387, 1986.
Valenzuela F, Aris H, Jacobelli S: Transient osteoporosis of the hip. J Rheum 4: 59–64. 1977.
Hongladarom T, Anderson DW: Transient painful osteoporosis of the hip. Con-temp Orthop 2: 148–154, 1980.
Goldenstein-Shainberg, Cossermelli W, Chu L et al. Arthritis as a manifestation of self-mutilation. J Rheum 19: 174–176, 1992.
Nellhaus G: Neurogenic arthropathies (Charcot’s joints) in children. Clin Pediatr 14: 647–653, 1975.
Dreyfuss JR, Glimcher MJ: Epiphyseal injury following frostbite. N Engl J Med 253: 1065–1068, 1955.
Carrera GF, Kozin F, McCarty DJ: Arthritis after frostbite injury in children Arthritis Rheum 22: 1082–1087, 1979.
Brown JP, Rola-Pleszczynski M, Menard H-A: Eosinophilic synovitis: clinical observations on a newly recognized subset of patients with dermatographism. Arthritis Rheum 29: 1147–1151, 1986.
Campbell AN, Freedman MH, McClure PD: Autoerythrocyte sensitization. J Pediatr 103: 157–160, 1983.
Clark GD, Key JD, Rutherford P, Bithoney WG: Munchausen’s syndrome by proxy (child abuse) presenting as apparent autoerythrocyte sensitization syndrome: An unusual presentation of Polle syndrome. Pediatrics 74: 1100–1102, 1984.
Sugai S, Yasuda Y, Shimizu S, et al.: DNA autosensitivity in two Japanese sisters. Arthritis Rheum 33: 287–292, 1990.
Ficat RP, Arlet J, Hungerford DS (eds.) Ischemia and Necrosis of Bone. Williams Wilkins, Baltimore, 1980, pp. 1–196.
Roy DR: Perthes-like changes caused by acquired hypothyroidism. Orthopedics 14: 901–904, 1991.
Editorial: Perthe’s disease. Lancet 1: 895–896, 1986.
Lowe TG: Scheuermann Disease. J Bone Joint Surg 72A: 940–945, 1990.
Siemsen JK, Brook J, Meister L: Lupus erythematosus and avascular bone necrosis. Arthritis Rheum 5: 492–501, 1962.
Fisher DE, Bickel WH: Corticosteroid-induced avascular necrosis. J Bone Joint Surg 53A: 813–859, 1971.
Editorial: crackling joints. Lancet 2:649, 1971.
Chondromalacia patellae. Lancet 1: 558–559, 1985.
Bourne MH, Hazel WA Jr, Scott SG, Sim FH: Anterior knee pain. Mayo Clin Proc 63: 482–491, 1988.
Arcoman JP, Kamhi E, Karas S, Moriarty VJ: Transchondral fracture and osteochonditis dessicans of talas. NYS J Med 78: 2183–2189, 1978.
Robinson RP, Franck WA, Carey EJ, Goldberg EB: Familial polyarticular osteochondritis dessicans masquerading as JRA. J Rheum 5: 190–194, 1978.
Ledwith CA, Fleisher GR: Slipped capital femoral epiphysis without hip pain leads to missed diagnosis, Pediatrics 89: 660–662, 1992.
Knowlton RG, Katzenstein PL, Moskowitz RW, et al.: Genetic linkage of a osteoarthritis associated with mild chondrodyplasia. N Eng J Med 322: 526530, 1990.
Brink SJ: Limited joint mobility as a risk factor for complications in youngsters with insulin-dependent diabetes mellitus. In: Pediatric and Adolescent Diabetes Mellitus. Chicago, Year Book, 1987, pp. 305–312.
Kapoor A, Sibbitt WL: Contractures in diabetes millitus: The syndrome of limited joint mobility. Semin Arthritis Rheum 18: 168–180, 1989.
Sherry DD, Rothstein RRL, Petty RE: Joint contractures preceding insulin-dependent diabetes mellitus. Arthritis Rheum 25: 1362–1364, 1982.
Costello PB, Tambar PK, Green FA: The prevalence and possible prognostic importance of arthropathy in childhood diabetes. J Rheumatol 11: 62–65, 1984.
Rosenbloom AL, Silverstein JH, Lezotte DC, et al.: Limited joint mobility in childhood diabetes mellitus indicates increased risk for microvascular disease. N Engl J Med 305:191–194, 1981 (see also editorial, pp. 217–219).
Rudolf MJC, Genel M, Tamborlane WV, et al.: Juvenile rheumatoid arthritis in children with diabetes mellitus. J Pediatr 99: 519–524, 1981.
Avioli LV, Krane SM: Metabolic Bone Disease. Vols. 1 and 2. Academic Press, New York, 1978.
Brenton DP, Dent CE: Idiopathic juvenile osteoporosis. In: Bickel H, Stern J (eds.) Inborn Errors of Calcium and Bone Metabolism University Park Press, Baltimore, 1976, pp. 222–238.
Smith R: Idiopathic juvenile osteoporosis. Am J Dis Child 133: 889–891, 1979.
Teotia M, Teotia SPS, Singh RK: Idiopathic juvenile osteoporosis. Am J Dis Child 133: 894–900, 1979.
Hoekman K, Papapoulos SE, Peters ACB, et al.: Characteristics and biphosphonate treatment of a patient with juvenile osteoporosis. J Clin Endocrinol Metab 61: 952–956, 1985.
Marder HK, Tsang RC, Hug G, Crawford AC: Calcitriol deficiency in idiopathic juvenile osteoporosis. Am J Dis Child 136: 914–917, 1982.
Cornelis F, Bardin T, Faller B, et al.; Rheumatic syndromes and /32 microglobulid amyloidosis in patients receiving long-term peritioneal dialysis. Arthritis Rheum 32: 785–788, 1989.
Bywaters EGL, Dixon ASTJ, Scott JT: Joint lesions of hyperparathyroidism. Ann Rheum Dis 22: 171–187, 1963.
Hunt PA, Wu-Chen ML, Handal NJ, et al.: Bone disease induced by anticonvulsant therapy and treatment with calcitriol (1,25-dihydroxyvitamin D3) Am J Dis Child 140: 715–718, 1986.
Siris ES, Clemens TL, Dempster DW, et al.: Tumor-induced osteomalacia. Kinetics of calcium, phosphorus, and vitamin D metabolism and characteristics of bone histomorphometry. Am J Med 82: 307–312, 1987.
Pollack JA, Schiller AL, Crawford JD: Rickets and myopathy cured by removal of a non-ossifying fibroma of bone. Pediatrics 52: 364–371, 1973.
Ryan EA, Reiss E: Oncogenous osteomalacia: review of the world literature of 42 cases and report of two new cases. Am J Med 77: 501–512, 1984.
Asnes RS, Berdon WE, Bassett CA: Hypophosphatemic rickets in an adolescent cured by excision of a non-ossifying fibroma. Clin Pediatr 20: 646–648, 1981.
Carey DE, Drezner MK, Hamdan JA, et al.: Hypophosphatemic rickets/ osteomalacia in linear sebaceous nevus syndrome: A variant of tumor induced osteomalacia. J Pediatr 109: 944–1000, 1986.
Silverton SF, Hadded JG: Medical reversal of acquired hypophosphatemic osteomalacia. Am J Med 82: 1077–1081, 1987.
Bland JH, Frymoyer JW: Rheumatic syndromes of myxedema. N Engl J Med 282: 1171–1173, 1970.
Hunter T, Chalmers IM, Dube WJ, et al.: Episodic polyarthralgia associated with Hashimoto’s thryroiditis. Arthritis Rheum 31: 303, 1988.
LeRiche NGH, Bell DA; Hashimoto’s thyroiditis and polyarthritis: A possible subset of seronegative polyarthritis. Ann Rheum Dis 43: 594–598, 1984.
Farbman K, Wheeler MF, Glick SR: Arthritis induced by antithyroid medica-tion. NY State J Med 69: 826–831, 1969.
Thomas J, Collipp PJ, Sharma RK: Thyroid acropachy. Am J Dis Child 125: 745–746, 1973.
Kingsley GH, Hickling P: Polyarthropathy associated with Cushing disease. Br Med J 292: 1363, 1986.
Calabrese, LH, White, CS: Musculoskeletal manifestations of Addison’s disease. Arthritis Rheum 22: 558, 1979.
Levy EN, Ramsey-Goldman R, Kahl LE: Adrenal insufficiency in two women with anticardiolipin antibodies. Cause and Effect? Arthritis Rheum 33: 1842 1846, 1990.
Pittsley RA, Yoder FW: Retinoid hyperostosis: skeletal toxicity associated with long-term administration of 13-cis-Retinoic acid for refractory ichthyosis. N Eng J Med 308:1012–1017, 1983 (see also editorial pp. 1024–1025).
Lippe B, Hensen L, Mendoza G, et al.: Chronic vitamin A intoxication. Am J Dis Child 125: 634–636, 1981.
DiGiovanna JJ, Helfgott RK, Gerber LH, Peck GL: Extraspinal tendon and ligament calcification associated with long-term therapy with etretinate. N Eng J Med 315: 1177–1182, 1986.
James MB, Leonard JC, Fraser JJ, Stuemky JH: Hypervitaminosis A: A Case Report. Pediatrics 69: 112–115, 1982.
Teotia M, Teotia SPS, Kunwar KB: Endemic skeletal fluorosis. Arch Dis Child 46: 686–691, 1971.
Bhussry BR, et al.: Toxic effects of larger doses of fluoride. in: Fluorides and Human Health. World Health Organization, Geneva, 1970, pp. 225–271.
Waldbott GL: Fluoride intoxication. JAMA 244: 331, 1980.
Christie DP: The spectrum of radiographic bone changes in children with fluorosis. Radiology 136: 85–90, 1980.
Fisher RL: Medcalf TW, Henderson MC: Endemic fluorosis with spinal cord compression. A case report and review. Arch Intern Med 149: 697–700, 1989.
Mason JO: A message to health professionals about fluorosis. JAMA 265: 2939, 1991.
Shapiro JR, Fallat RW, Tsang RC: Achilles tendinitis and tenosynovitis: a diagnostic manifestation of familial type II hyperlipoproteinemia in children. Am J Dis Child 128: 486–490, 1974.
Buckingham RB, Bde GG, Bassett DR: Polyarthritis associated with type IV hyper-lipoproteinemia. Arch Intern Med 135: 286–290, 1975.
Bjorkhem I, Skrede S: Familial diseases with more storage of sterols than cholesterol: cerebrotendinous xanthomatosis and phytosterolemia. In Scriver CR, Beaudet AL, Sly WS, Valle D (eds.) The Metabolic Basis of Inherited Disease, 6th ed. McGraw-Hill, 1989, pp. 724–730.
Belamarich PF, Deckelbaum RJ, Starc TJ, et al.: Response to diet and cholestyramine in a boy with sitosterolemia. Pediatrics 86: 977–981, 1990.
Stapleton FB, Nyhan WL, Borden M, Kaufman IA: Renal pathogenesis of familial hyperuricemia: studies in two kindreds. Pediatr Res 15: 1447–1453, 1981.
Middlemiss JH, Braband H: Juvenile gout. Clin Radio! 13: 149–152, 1962.
Decker JL, Vandeman PR: Renal calculi preceding gouty arthritis in a child. Am J Med 32: 805–810, 1962.
Vora S: Isozymes of phosphofructokinase. Isozymes: current topics in biological and medical research. 6: 119–167, 1982.
Liberman UA, Samuel R, Halabe A, el al.: Juvenile metabolic gout caused by chronic compensated hemolytic syndrome. Arthritis Rheum 25: 1264–1266, 1982.
Harlan WR, Cornoni-Huntley J, Leaverton PE: Physiologic determinants of serum urate levels in adolescence. Pediatrics 63: 569–575, 1979.
Boss GR, SeegmillerJE: Hyperuricemia and gout: Classification, complications and management. N Engl Med 300: 1459–1468, 1979.
Kelley WN: Hyperuricemia. In Kelley WN, Harris ED Jr, Ruddy S, Sledge CB (eds.) Textbook of Rheumatology. Saunders, Philadelphia, 1989, pp. 13951436.
Rosenblatt D, Homes LB: Development of arthritis in Lowe’s syndrome. J Pediatr 85: 924–925, 1974.
Athreya BH, Schumacher HR, Getz HD, et al.: Arthropathy of Lowe’s (oculocerebrorenal) syndrome. Arthritis Rheum 26: 728–736, 1983.
Kaplan P, Kitschner M, Watters G, Costa MT: Contractures in patients with Williams syndrome. Pediatrics 84: 895–899, 1989.
Bensen WG, Laskin CA, Little HA, et al.: Hemochromatoric arthropathy mimicking rheumatoid arthritis. Arthritis Rheum 21: 844–848, 1978.
Goldschmidt H, Spiera H, Schumacher HR, Zaroulis CG: Idiopathic hemochromatosis presenting as amenorrhea and arthritis. Am J Med 82: 1057 1059, 1987.
Kidd KK: Genetic linkage and hemochromatosis. New Engl J Med 301: 209210, 1979.
Nesterov AI: The clinical course of Kashin-Beck disease. Arthritis Rheum 7: 2940, 1964.
Takamori T: Kaschin-Beck’s disease. The Professor Tokio Takamori Foundation, Gifu University School of Medicine, Japan, 1968 (2 vols).
Sokoloff L: The history of Kashin-Beck disease. NYS J Med 89: 343–351, 1989.
Mseleni Joint Disease. Editorial. Lancet 2: 483–484, 1985.
Reginato AJ: Articular chondrocalcinosis in the Chiloe Islanders. Arthritis Rheum 19: 395–404, 1976.
Mirahmadi KS, Coburn JW, Bluestone R: Calcific periarthritis and hemodialysis. JAMA 223: 548–549, 1973.
Diggs LW: Bone and joint lesions in sickle cell disease. Clin Orthop 52: 119–143, 1976.
Duthie RB, Rizza CR: Rheumatologic manifestations of the hemophilias. Clin Rheum Dis 1: 53–93, 1975.
Johnson CR, Corrigan JJ, Gall EP: Treatment of hemophilia arthritis with D-penicillamine. Arthritis Rheum 33: 5111, 1990.
Klofkorn RW, Lightsey AL: Hemarthrosis associated with Glanzmann’s thrombastenia. Arthritis Rheum 22: 1390–1393, 1979.
Wilfert CM, Buckley RH, Mohanakumar T, et al.: Persistent and fatal central nervous system echovirus infections in patients with agammaglobulinemia. N Engl J Med 296: 1485–1489, 1977.
Ammann AJ, Wara DW, Pillarisetty RJ, Talai N: The prevalence of autoantibodies in T-cell, B-cell, and phagocytic immunodeficiency disorders. Clin Immunol Immunopathol 14: 456–466, 1979.
Fraser KJ, Clarris BJ, Muirden KD, et al.: A persistent adenovirus type 1 infection in synovial tissue from an immunodeficient patient with chronic, rheumatoid-like polyarthritis. Arthritis Rheum 28: 455–458, 1985.
Case records of the Massachusetts General Hospital: Case 34–1988. N Eng J Med 319: 495–509, 1988.
Cassidy JT, Petty RE, Sullivan DB: Occurrence of selective IgA deficiency in children with JRA. Arthritis Rheum 20: 181–183, 1977.
Pelkonen P, Savilahti E, Makela A-L: Persistent and transient IgA deficiency in juvenile rheumatoid arthritis. Scand J Rheumatol 12: 273–279, 1983.
Levitt D, Cooper M: Immunoregulatory defects in a family with selective IgA deficiency. J Pediatr 98: 52–58, 1981.
Schopfer K, Feldges A, Baerlocher K, et al.: Systemic lupus erythematosus in Staphylococcus aureus hyperimmunoglobulinemia E syndrome. Br Med J 287: 524–526, 1983.
Rodney GE, Park BH, Ford D, et al.: Defective bactericidal activity of peripheral blood leukocytes in lipochrome histiocytosis. Am J Med 49: 322–327, 1970.
Schaller JG: Arthritis and immunodeficiency. Arthritis Rheum 20: 443–445, 1979.
Manzi S, Urbach AH, McCune AB, et al.: Systemic lupus erythematosus in a boy with chronic granulomatosus disease: case report and review of the literature. Arthritis Rheum 34: 101–105, 1991.
Jacobs JC, Goetzl EJ: “Streaking leukocyte factor,” arthritis and pyoderma gangrenosum. Pediatrics 56: 570–578, 1975.
Abu-Elmagd K, Jegasothy BV, Ackerman CD, et al.: Efficacy of FK 506 in the treatment of recalcitrant pyoderma gangrenosum. Transplant Proc 23: 33283329, 1991.
Elgart G, Stover P, Larson K et al. Treatment of pyoderma gangrenosum with cyclosporine: Results in seven patients. J Am Acad Dermatol 24: 83–86, 1991.
Jacobs JC: Hypergammaglobulinemic purpura in a child. J Pediatr 87: 91–93, 1975.
Ferreiro JE, Pasarin G, Quesada R, Gould E: Benign hypergammaglobulinemic purpura of Waldenstrom associated with Sjogren’s syndrome. Am J Med 81: 734–740, 1986.
Sim TC, Grant JA: Hereditary angioedema: its diagnostic and management perspectives. Am J Med 88: 656–664, 1990.
Stoppa-Lyonnet D, Tosi M, Laurent J, et al.: Altered Cl inhibitor genes in type 1 hereditary angioedema. N Eng J Med 317:1–6, 1987 (see also pp. 43–44: editorials).
Ley SJ, Williams RC Jr: A family with hereditary angioedema and multiple immunologic disorders. Am J Med 82: 1046–1051, 1987.
Pan CC, Ward MK, Spitzer R, et al.: Non-SLE glomerulonephritis associated with hereditary angioedema: long-term follow-up. Pediatr Res 27 # 2: 335A, 1990.
Frigas E: Angiedema with acquired deficiency of the C 1 inhibitor: a constellation of syndromes. Mayo Clin Proc 64: 1269–1275, 1989.
Alsenz J, Bork K Loos M: Autoantibody-mediated acquired deficiency of Cl Inhibitor. N EngJ Med 316: 1360–1366, 1987.
Brown JP, Rola-Pleszczynski M, Menard H-A: Eosinophilic synovitis: clinical observations on a newly recognized subset of patients with dermatographism. Arthritis Rheum 29: 1147–1151, 1986.
Grandel KE, Farr RS, Wanderer AA, et al.: Association of platelet-activating factor with primary acquired cold urticaria. N Eng J Med 313: 405–409, 1985.
Ireland TA, Werner DA, Rietschel RL, et al.: Cutaneous lesins in cryofibrinogenemia. J Pediatr 105: 67–70, 1984.
Ratner D, Eshel E, Vigder K: Juvenile rheumatoid arthritis and milk allergy. J R Soc Med 78: 410–413, 1985.
Brady JE: Rheumatoid arthritis and food allergy: a review of the scientific literature. Food Allergy Update Newsletter 6: 1–8, 1989.
Panush RS: Food induced (“allergic”) arthritis: clinical and serologic studies. 17: 291–294, 1990.
Beni D, Malaviya AN, Shandilya R, Singh RR: Effect of dietary restrictions on disease activity in rheumatoid arthritis. Ann Intern Med 47: 69–72, 1988.
Bowen J, Boudoulas H, Wooley CF: Cardiovascular disease of connective tissue origin. Am J Med 82: 481–488, 1990.
Boucek RJ, Noble NL, Gunj a-Smith Z, et al.: The Marfan syndrome: A deficiency in chemically stable collagen cross-links. N Engl J Med 305: 988–991, 1981.
Gott VL, Pyertiz RE, Magovern GJ, et al.: Surgical treatment of aneursyms of the ascending aorta in the Marfan syndrome. N Eng J Med 314: 1070–1074, 1986.
Brody JE: Personal health. The New York Times. March 12, 1986.
McKusick VM: Heritable Disorders of Connective Tissue, 4th ed. Mosby, St. Louis, 1972.
Byers PH, Holbrook KA: Molecular basis of clinical heterogeneity in the Ehlers-Danlos Syndrome. Ann NY Acad Sci 460: 298–310, 1985.
Hollister D: Heritable disorders of connective tissue: Ehlers-Danlos syndrome. Pediatr Clin North Am 25: 575–591, 1978.
Bertin PH, Treves R, Julia A, et al.: Ehlers-Danlos syndrome, clotting disorder and muscular dystrophy. Ann Rheum Dis 48: 953–956, 1989.
Wenstrup RJ, Murad S, Pinnell SR: Ehlers-Danlos syndrome type VI: Clinical manifestations of collagen lysyl hydroxylase deficiency. J Pediatr 115: 405–409, 1989.
Beighton P, Grahama R, Bird H: Hypermobility of joints. Springer-Velag, Berlin, Heidelberg, pp. 1–178, 1983.
Byers PH, Siegel RC, Holbrook KA, et al.: X-linked cutis laxa. Defective cross-link formation in collagen due to decreased lysyl oxidase activity. New Engl J Med 303: 61–65, 1980.
Bowen J, Boudulas H, Wooley CF: Cardiovascular disease of connective tissue origin. Am J Med 82: 481–488, 1990.
Glesby MJ, Pyeritz RE: Association of mitral valve prolapse and systemic abnormalities of connective tissue. A phenotypic continuum. JAMA 262: 523528, 1989.
Harinstein D, Buckingham RB, Braun T, et al.: Systemic joint laxity (the hypermobile joint syndrome) is associated with temporomandibular joint dysfunction. Ann Rheum Dis 47: 254, 1988.
Lewkonia RM, Ansell BM: Articular hypermobility simulating chronic rheumatic disease. Arch Dis Child 58: 988–992, 1983.
Biro F, Gewanter HL, Baum J: The hypermobility syndrome. Pediatrics 72: 701–706, 1983.
Holzberg M, Hewan-Lowe KO, Olansky AJ: The Ehlers-Danlos syndrome: Recognition, characterization, and importance of a milder variant of the classic form. J Ma Acad Dermatol 19: 656–666, 1988.
Arroyo IL, Brewer EJ, Giannini EH: Arthritis/arthralgia and hypermobility of the joints in school children. J Rheumatol 15: 978–980, 1988.
Gedalia A, Press J. Articular symptoms in hypermobile schoolchildren: A prospective study. J Pediatr 119: 944–946, 1991.
Grana WA, Moretz JA: Ligamentous laxity in secondary school athletes. JAMA 240: 1975–1976, 1978.
Jessee EF, Owen DS Jr., Sagar KB: The benign hypermobile joint syndrome. Arthritis Rheum 23: 1053–1056, 1980.
Dacre JE, Huskisson EC: Arthritis in Down’s syndrome. Ann Rheum Dis 47: 254–255, 1988.
Yancey CL, Smijewski C, Athreya BH, Doughty RA: Arthropathy of Down’s syndrome. Arthritis Rheum 27: 929–934, 1984.
Olson JC, Bender JC, Levinson JE, et al.: Arthropathy of Down syndrome. Pediatrics 86: 931–936, 1990.
Petty RE, Malleson P, Kalousek DK: Chronic arthritis in two children with partial deletion of chromosome 18. J Rheumatol 14: 586–587, 1987.
Balestrazzi P, Gerraccioli GF, Ambanelli U, Giovannelli G: Juvenile rheumatoid arthritis in Turner’s syndrome. Clin Exp Rheumatol 4: 61–62, 1986.
Beighton P: Inherited Disorders of the Skeleton. Churchill Livingstone, New York, 1978.
Beighton P, De Paepe A, Dawks D, et al.: International nosology of heritable conditions of connective tissue. Am J Med Genet 29: 581–594, 1988.
Valduea AF: The nail-patella syndrome. J Bone Joint Surg 55B: 145–162, 1973.
Letts M: Hereditary onycho-osteodysplasia (nail-patella syndrome). A three-generation familial study. Orthopaed Rev 20: 267–272, 1991.
Petajan JH, Momberger GL, Aase J, et al.: Arthrogryposis syndrome (Kuskokwim disease) in the eskimo. JAMA 209: 1481–1486, 1969.
Jones KL: The fetal alcohol syndrome. Addictive Diseases 2: 79–88, 1975.
Mirise RT, Shear S: Congenital contractual arachnodactyly. Arthritis Rheum 22: 542–546, 1979.
Ardinger HH, Hanson JW, Harrod MJE, et al.: Further delineation of Weaver Syndrome. J Pediatr 108: 228–235, 1986.
Abe K, Niikawa N, Sasaki H: Zollinger-Ellison syndrome with Marden-Walker syndrome. Am J Dis Child 133: 735–738, 1979.
Esterly NB, McKusick VA: Stiff skin syndrome. Pediatrics 47: 360–369, 1971.
Solimena M, Folli F, Denis-Donino S, et al.: Autoantibodies to glutamic acid decardoxylase in a patient with stiff-man syndrome, epilepsy, and type 1 diabetes mellitus. N Eng J Med 318:1012–1220, 1988 (see also editorial pp. 1060–1061).
Liberfarb RM, Hirose T, Holmes LB: The Wagner-Stickler syndrome: a study of 22 families. J Pediatr 99: 394–399, 1981.
Omdal R, Laerdal A, Kjellwvold KH: Milticentric reticulohistiocytosis in a 9-year-old boy. Arthritis Rheum 31: 1588–1590, 1988.
Raphael SA, Cowdery SL, Faerber EN, et al.: Multicentric reticulohistiocytosis in a child. J Pediatr 266–269, 1989.
Zayid I, Farraj J: Familial histocytic dermatoarthritis. Am J Med 54: 793–800, 1973.
Stowens DW, Teitelbaum SL, Kahn AJ, Barranger JA: Skeletal complications of Gaucher disease. Medicine 64: 310–322, 1985.
Nightingale SL: Alglucerase approved for Gaucher’s disease. JAMA 265: 2934, 1991
Katz K, Cohen JI, Zib N, et al.: Fractures in children who have Gaucher disease. J Bone Joint Surg 69A: 1361–1370, 1987.
Sheth KJ, Bernhard GC: The arthropathy of Fabry disease. Arthritis Rheum 22: 781–783, 1979.
von Scheidt W, Eng CM, Fitzmaurice TF, et al.: An atypical variant of Fabry’s disease with manifestations confined to the myocardium. N Eng J Med 324: 395–399, 1991.
Abul-Haj SK, Martz DG, Douglas WF, et al.: Farber’s disease: Report of a case with observations on its histogenesis and notes on the nature of the stored material. J Pediatr 61: 221–232, 1962.
Moser HW: Ceramidase deficiency: Farber’s lipogranulomatosis. In Stanbury JB, Wyngaarden JB, Frederickson DS (eds.) The Metabolic Basis Inherited Disease, 4th ed. McGraw Hill, New York, 1989, pp. 1645–1653.
Ben-Yoseph Y, Gagne R, Parvathy MR, et al.: Diagnosis and carrier detection of Farber disease (ceramidase deficiency) in plasma and leukocytes. Pediatr Res 255: 139A, 1989.
Katzenstein PL, Malemud CJ, Pathria M, et al.: Early-onset primary osteoarthritis and mild chondrodysplasia: radiographic and pathologic studies with an analysis of cartilage proteoglycans. Arthritis Rheum 33: 674–684, 1990.
Spranger JW, Langer LO, Wiedermann MD: Bone Dysplasias. Saunders, Philadelphia, 1974.
Spranger J, Albert C, Schilling F et al. Progressive pseudorheumatoid arthritis of childhood. Eur J Pediatr 140: 34–40, 1983.
Wynne-Davis R, Gormley J: the prevalence of skeletal dysplasias: an estimate of the minimum frequency and the number of patients requiring orthopedic care. J Bone Joint Surg 67B: 133–137, 1985.
Patrone NA, Kredich DW: Arthritis in children with multiple epiphyseal dysplasia. J Rheumatol 12: 145–149, 1985.
Knowlton RG, Katzenstein PL, Moskowitz RW, et al.: Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodyplasia. N Eng J Med 322: 526–530, 1990.
Morris L, Kozlowski K, McNaught P, Silink M: Tricho-rhino-phalangeal syndrome I. Australas Radiol 29: 167–173, 1985.
Stearns ZR, Lacassie Y, MacEwen GD: Perthes-like disease and the trichorhino-phalangeal syndromes: The first black patient. Orthopedics 13: 468–473, 1990.
McGuire RA Jr., Reinert CM: Hereditary multiple exostosis. Orthop Rev 16: 29–34, 1985.
Lackman RS, Cohen A, Hollister D, et al.: Metachrondromatosis. In: Skeletal Dysplasias. Birth Defects 10:171–178, 1974.
Gorham LW, Stout AP: Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone). Its relation to hemangiomatosis. J Bone Joint Surg 37A: 985–1004, 1955.
Erickson CM, Hirschbever M, Stickler GB: Carpal-tarsal osteolysis. J Pediatr 93: 779–782, 1978.
Udell J, Schumacher HR, Kaplan F, Fallon MD: Idiopathic familial acroosteolysis: Histomorphometric study of bone and literature review of the HajduCheney Syndrome. Arthritis Rheum 29: 1032–1038, 1986.
Shurtieff DB, Sparkes RS, Clawson K, et al.: Hereditary osteolysis with hypertension and nephropathy. JAMA 188: 363–368, 1964.
Hollister DW, Rimoin DL, Lachman RS, et al.: The Winchester syndrome: A non-lysosomal connective tissue disease. J Pediatr 84: 701–709, 1974.
Prieur AM, Griscelli C, Lampert F, et al.: A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. J Rheumatol 66: 57–68, 1987.
Brueton LA, Sanderson IR, Jadresic L, et al.: An infant with chronic articular and cutaneous manifestations: a new syndrome? Proc Roy Soc 82: 223–225, 1989.
Glover MT, Lake BD, Atherton DJ: Infantile systemic hyalinosis: Newly recognized disorder of collagen? Pediatrics 87: 228–234, 1991.
Jacobs JC, Downey JA: Juvenile rheumatoid arthritis. In: Downey JA, Low NL (eds.) The Child with Disabling Illness. Saunders, Philadelphia, 1974, pp. 524.
Jacobs JC, Phillips PE, Johnston AD: Needle biopsy of the synovium of children. Pediatrics 57: 696–701, 1976.
Athreya BH, Schumacher HR: Pathologic features of a familial arthropathy associated with congential flexion contractures of fingers. Arthritis Rheum 21: 429–437, 1978.
Schubiner JM, Simon MA: Primary bone tumors in children. Ortho Cl NA 18: 577–595, 1987.
Aprin H: Benign Chondroblastoma. Orthopedics 4: 1134–1140, 1981.
Altman B, Ruby LK: Plexiform neurofibroma presenting as wrist synovitis. A case report. Orthopedics 5: 1333–1335, 1982.
Orlowski JP, Mercer RD: Osteoid osteoma in children and young adults. Pediatrics 59: 526–532, 1977.
Saville PD: A medical option for the treatment of osteoid osteoma. J Pediatr 66: 1409–1411, 1980.
Cohen MD, Harrington TM, Ginsburg WW: Osteoid osteoma: 95 cases and a review of the literature. Semin Arthritis Rheum 12: 265–281, 1983.
Haueisen DC, Weiner DS, Weiner SD: The characterization of “transient synovitis of the hip” in children. J Pediatr Orthop 6: 11–17, 1986.
Osteoid osteoma: elements of diagnosis and treatment. Contemp Orthopaed 18:461–467, 1989.
Voto SJ, Cook AJ, Ewing JW, Weiner DS: CT-guided excision as a treatment for osteoid osteoma. Surg Rounds Orthopaed, pp. 31–36, February 1990.
Gerber NJ, Dixon St J: Synovial cysts and juxta-articular bone cysts (geodes). Semin Arthritis Rheum 3: 323–348, 1974.
Medical World News, February 11, 1972, p. 50E.
O’Dell JR, Andersen PA, Hollister JR, West SG: Anterior tibial mass: an unusual complication of popliteal cysts. Arthritis Rheum 27: 113–115, 1984.
Lewis RC, Coventry MB, Soule EH: Hemangioma of the synovial membrane. J Bone Joint Surg 41A: 264–271, 1959.
Moon NF: Synovial hemangioma of the knee joint. Clin Orthop 90: 183–190, 1973.
Linsons MA: Synovial hemangioma as a cause of recurrent knee effusions. JAMA 242: 2214–2215, 1979.
Visuri T: Recurrent spontaneous haemarthrosis of the knee associated with a synovial and juxta-articular haemangiohamartoma. Ann Rheum Dis 49: 554556, 1990.
Docken WP: Pigmented villonodular synovitis: A review with illustrative case reports. Semin Arthritis Rheum 9: 1–22, 1979.
Flandry F, Hughston JC: Pigmented villonodular synovitis. J Bone Joint Surg 69A: 942–949, 1987.
Hajdu SI: Differential diagnosis of soft tissue and bone tumors. Philadelphia, Lea Febiger, 1986.
Ladisch S, Jaffe ES. The histiocytoses. In Pizzo P, Poplack DG (eds) Pediatric Oncology. Philadelphia: J. B. Lippincott, 1988, pp. 491–504.
Israels SJ, Chan HL, Daneman A, Weitzman SS: Synovial sarcoma in childhood. AJR 142: 803–806, 1984.
Case records of the Massachusetts General Hospital: Case 10–1990. N Eng J Med 683–690, 1990.
Menendez LR, Brien E, Brien WW. Synovial sarcoma. Orthop Rev 21: 465471, 1992.
Rosenberg AM: Analysis of a pediatric rheumatology clinic population. J Rheumatol 17: 827–830, 1990.
Ehrlich EL, Fisher RL: Orthopedic conversion reactions in children and adolescents. Conn Med 41: 681–683, 1977.
Maisami M, Freeman JM. Conversion reactions as body language. Pediatrics 80: 46–52, 1987.
Sills EM: “Rheumatic” syndromes of obscure origin. (Editorial.) J Pediatr 120:675, 1988.
Sherry DD, McGuire T, Mellins E, et al.: Psychosomatic musculoskeletal pain in childhood: Clinical and psychological analyses of 100 children. Pediatrics 88: 1093–1099, 1991.
Maisami M, Freeman JM: Conversion reactions in children as body language: a combined child psychiatry/neurology team approach to the management of functional neurologic disorders in children. Pediatrics 80: 46–52, 1987.
Libow JA, Schreier HA: Three forms of factitious illness in children: When is it Munchausen syndrome by proxy? Am J Orthopsychiat 56: 602–611, 1986.
Block SR: Fibrositis and the concept of generalized rheumatism: the confessions of an unrepentant lumper. Occupational Problems in Medical Practice 5 (#3): 1–6, 1990.
Thompson JM: Tension myalgia as a diagnosis at the Mayo Clinic and its relationship to fibrositis, fibromyalgia, and myofascial pain syndrome. Mayo Clin Proc 65: 1237–1248, 1990.
Wolfe F, Smythe HA, Yunus MB, et al.: The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee. Arthritis Rheum 33: 160–171, 1990.
Hadler NM: A critical reappraisal of the fibrositis concept. In Bennett RM (ed.) The fibrositis/fibromyalgia syndrome. Current issues and perspectives. Am J Med 81: Suppl. 3A:1–115, 1986.
Hadler NM: The plight of the patient whose illness is labeled as fibrositis or a related paralogism. Occupational Problems in Medical Practice 5 (#3): 6–8, 1990.
Bernstein BH, Singsen BH, Kent JT, et al.: Reflex neurovascular dystrophy in childhood. J Pediatr 93: 211–215, 1978.
Gold S: Diagnosis and management of hysterical contracture in children. Br Med J 1: 21–23, 1965.
Goldsmith DP, Vivino FB, Eichenfield AH, et al.: Nuclear imaging and clinical features of childhood reflex neurovascular dystrophy: Comparison with adults. Arthritis Rheum 32: 480–485, 1989.
Sherry DD, Weisman R: Psychologie aspects of childhood reflex neurovascular dystrophy. Pediatrics 81: 572–578, 1988.
Hyler SE, Sussman N: Chronic factitious disorder with physical symptoms (the Munchausen syndrome). Psychiatric Clin North Am 4: 365–377, 1981.
Batshaw ML, Wachtel RC, Deckel AW, et al.: Munchausen’s syndrome simulating torsion dystonia. N EngJ Med 312: 1437–1439, 1985.
Lane TJ, Manu P, Matthews DA: Depression and somatization in the chronic fatigue syndrome. Am J Med 91: 335–344, 1991.
Katz BZ, Andiman WA: Chronic fatigue syndrome. Current literature and clinical issues. J Pediatr 113: 944–947, 1988.
Gold R, Sixbey J, et al.: Chronic fatigue: a prospective clinical and virologie study. JAMA 264: 48–53, 1990.
Shafran SD: The chronic fatigue syndrome. Am J Med 90: 730–739, 1991.
Paperny D, Hicks R, Hammar SL: Munchausen’s syndrome. Am J Dis Child 134: 794–795, 1980.
Aduan RP, Fauci AS, Dale DC, et al.: Factitious fever and self-induced infection. Ann Intern Med 90: 230–242, 1979.
Reich P, Gottfried LA: Factitious disorders in a teaching hospital. Ann Intern Med 99: 240–247, 1983.
Meadow R: Factitious illness—the hinterland of child abuse. In Recent Advances in Pediatrics, No. 7, Churchill Livingston, New York, 1984, pp. 217232.
Zitelli BJ, Seltman MF, Shannon RM: Munchausen’s syndrome by proxy and its professional participants. Am J Dis Child 141: 1099–1102, 1987.
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Jacobs, J.C. (1993). The Differential Diagnosis of Arthritis in Childhood. In: Pediatric Rheumatology for the Practitioner. Springer, New York, NY. https://doi.org/10.1007/978-1-4757-6150-4_2
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