Abstract
Malformation denotes an abnormal structure that results from an aberration in embryologic development. Although the term malformation is conventionally used as a synonym for hamartoma, the two are different, because hamartoma refers to a potpourri of tissue elements normally present at a particular site. Vascular malformations can be either functional or anatomic. In the case of functional abnormalities, the changes are related mostly to physiologic changes, as is the case for nevus anemicus. In contrast, anatomic vascular malformations exhibit evident morphologic abnormalities of the involved vessels. Anatomic vascular malformations are subdivided into the following groups: capillary, venous, arterial, lymphatic, and combined anomalies (Table 1). Clinically, it is important to separate the vascular malformations into those of low flow and high flow. Low-flow abnormalities include malformations of capillary, venous, lymphatic, or combination, whereas high-flow abnormalities include arteriovenous malformations (1).
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References
Mulliken JB. Classification of vascular birthmarks. In: Mulliken JB, Young AE, eds. Vascular Birthmarks. Hemangiomas and Malformations. Philadelphia, WB Saunders, 1988;24–37.
Greaves MW, Birkett D, Johson C. Nevus anemicus: a unique catecholamine-dependent nevus. Arch Dermatol 1970;102:172–6.
Daniel RH, Hubler WR, Wolf JE, et al. Nevus anemicus: donor-dominant defect. Arch Dermatol 1977;113:53–6.
Mountcastle EA, Diestelmeier RM, Lupton GP. Nevus anemicus. J Am Acad Dermatol 1986;14:628–32.
Fleischer TL, Zeligman I. Nevus anemicus. Arch Dermatol 1969;100:750–5.
Ratz JL, Roenigk HH Jr. Multiple vascular anomalies: report of a case. J Dermatol Surg Oncol 1978;4:684–6.
Raff M. Die Bedeutung adrenerger Rezeptoren fur die Entstehung des naevus flammeus und des Naevus anaemicus. Wien Klin Wochenschr 1981;129(suppl):1–14.
Dupre A, Bonafe JL, Jouas H. Naevus anemique generalisé acquis. Dermatologica 1981;163:276–81.
Davies MG, Greaves MW, Coutss A, Black AK. Nevus oligemicus. A variant of nevus anemicus. Arch Dermatol 1981;117:111–3.
Hidano A, Arai Y. Hémihypertrophie congénitale associée à des anomalies cutanées pigmentovasculaires, cérébrales, viscèrales et squelettiques. Ann Dermatol Venereol 1987;114:665–9.
Happle R. Allelic somatic mutations may explain vascular twin nevi. Hum Genet 1991;86:321–3.
Mizutani H, Ohyanagi S, Umeda Y, Shimizu M, Kupper TS. Loss of cutaneous delayed hypersensitivity reactions in nevus anemicus. Evidence for close concordance of cutaneous delayed hypersensitivity and encdnthelial F-celertin exnrescion Arch Dermatol 1997:133:617–20.
Di Landro A, Tadini GL, Marchesi L, Cainelli T. Phakomatosis pigmentovascularis. a new case with renal angiomas and some considerations about the classification. Pediatr Dermatol 1999;16:25–30.
Ahkami RN, Schwartz RA. Nevus anemicus. Dermatology 1999;198:327–9.
Hasegawa Y, Yasuhara M. Phakomatosis pigmentovascularis type IVa. Arch Dermatol 1985;121:651–5.
Miura Y, Tajima S, Ishibashi A, Hata Y. Multiple anemic macules on the arms: a variant form of nevus anemicus? Dermatology 2000;201:180–3.
Plantin P, Schoenlaub P. Multiple anemic macules on the arms: not a variant form of nevus anemicus. Dermatology 2001;202:271–2.
van Lohuizen CHJ. Über eine seltene angeborene Hautanomalie (cutis marmorata telangiectatica congenita). Acta Derm Venereol 1922;3:202–11.
Brain RT. Naevus vascularis reticularis. Proc Soc Med 1954;47:172–3.
Andreev VC, Pramatarov K. Cutis mamorata telangiectatica congenita in two sisters. Br J Dermatol 1979;101:345–50.
Kurczinski TW. Hereditary cutis marmorata telangiectatica congenita. Pediatrics 1982;70:52–3.
Way BH, Herrmann, J, Gilbert EF, et al. Cutis marmorata telangiectatica congenita. J Cutan Pathol 1974;1:10–25.
Rogers M, Poyzer KG. Cutis marmorata telangiectatica congenita. Arch Dermatol 1982;118:895–9.
Suarez SM, Grossman ME. Localized cutis marmorata telangiectatica congenita. Pediatr Dermatol 1991;8:329–31.
Devillers AC, de Waard-van der Spek FB, Oranje AP. Cutis marmorata telangiectatica congenita: clinical features in 35 cases. Arch Dermatol 1999;135:34–8
Amitai DB, Fichman S, Merlob P, Morad Y, Lapidoth M, Metzker A. Cutis marmorata telangiectatica congenita: clinical findings in 85 patients. Pediatr Dermatol 2000;17:100–4.
Enjolras O. Cutis marmorata telangiectatica congenita. Ann Dermatol Venereol 2001;128:161–6
Sanchez P, Bosch RJ, Herrera E. Cutis marmorata telangiectatica congenita: forme dimelique croisée. Ann Dermatol Venereol 1992;119:647–50.
Picascia DD, Esterly NB. Cutis marmorata telangiectatica congenita: report of 22 cases. J Am Acad Dermatol 1989;20:1098–104.
Petrozzi WJ, Rahn EK, Mofenson H, et al. Cutis marmorata telangiectatica congenita. Arch Dermatol 1970;101:74–7.
Lee S, Lee JB, Kim JH, et al. Cutis marmorata congenita with multiple congenital abnormalities (van Lohuizen’ s syndrome). Dermatologica 1981:163:408–12.
Lopez-Herce Cid J, Roche Herrero MC, Pascual Castroviejo I. Cutis marmorata telangiectatica congenita. Anomalias asociadas. An Estp Pediatr 1985:22:585–90.
Gerritsen MJ, Steijlen PM, Brunner HG, Rieu P. Cutis marmorata telangiectatica congenita: report of 18 cases. Br J Dermatol 2000;142:366–9.
Sato SE, Herschler J, Lynch PJ, et al. Congenital glaucoma associated with cutis marmorata congenita telangiectatica: two case reports. J Pediatr Ophthalmol Strabismus 1988;25:13–7.
Vazquez F, Lopez B, Requena L, Garcia Perez A. Congenital glaucoma and cutis marmorata telangiectasia: report of the second case. Dermatologica 1989;177:193–4.
Lynch PJ. Cutis marmorata telangiectatica congenita associated with congenital glaucoma. J Am Acad Dermatol 1990;22:857.
Miranda I, Alonso MJ, Jimenez M, Tomas-Barberan S, Ferro M, Ruiz R. Cutis marmorata telangiectatica congenita and glaucoma. Ophthalmic Paediatr Genet 1990;11:129–32.
Kremer I, Metzker A, Yassur Y. Intraoperative suprachoroidal hemorrhage in congenital glaucoma associated with cutis marmorata telangiectatica congenita. Arch Ophthalmol 1991;109:1199–200.
Weilepp AE, Eichenfield LF. Association of glaucoma with cutis marmorata telangiectatica congenita: a localized anatomic malformation. J Am Acad Dermatol 1996;35:276–8.
South DA, Jacobs AH. Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia). J Pediatr 1978:93:944–9.
Wong V. Cutis marmorata telangiectatica congenita: an unusual presentation with monoatrophy in two Chinese children. J Paediatr Child Health 1997;33:71–3.
Stephan MJ, Hall BD, Smith DW, Cohen MM Jr. Macrocephaly in association with unusual cutaneous angiomatosis. J Pediatr 1975;87:353–9.
Moore CA, Torriello HV, Abuelo DN, et al. Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities. Am J Med Genet 1997;2:67–73.
Wroblewski I, Joannard A, Francois P, Baudain P, Beani JC, Beaudoing A. Cutis marmorata telangiectatica congenita avec asymétrie corporalle. Pediatrie 1988;43:117–20
Clayton-Smith J, Kerr B, Brunner H, et al. Macrocephaly with cutis marmorata, haemangioma and syndactyly-a distinctive overgrowth syndrome. Clin Dysmorphol 1997;6:291–302.
Carcao M, Blaser SI, Grant RM, Weksberg R, Siegel-Bartelt J. MRI findings in macrocephaly-cutis marmorata telangiectatica congenita. Am J Med Genet 1998;76:165–7.
Vogels A, Devriendt K, Legius E, et al. The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-un data in 4 children adolescents. Genet Couns 1998;9: 245–53
Robertson SP, Gattas M, Rogers M, Ades LC. Macrocephaly-cutis marmorata telangiectatica congenita: report of five patients and a review of the literature. Clin Dysmorphol 2000;9:1–9.
Franceschini P, Licata D, Di Cara G, Gaula A, Franceschini D, Genitori L. Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata? Am J Med Genet 2000;14:265–9.
Yano S, Watanabe Y. Association of arrhythmia and sudden death in macrocephaly-cutis marmorata telangiectatica congenita syndrome. Am J Med Genet 2001;102:149–52.
Gelmetti C, Console V, Schianchi R, Missaglia R. Cutis marmorata telangiectatica congenita. Descrizione di un nuovo caso. Pediatr Med Chir 1986;8:907–9.
Gelmetti C, Schianchi R, Ermacora E. Cutis marmorata telangiectatica congenita. Quatre nouveaux cas et revue de la littérature. Ann Dermatol Venereol 1987;114:1517–28.
Del Giudice SM, Nydorf ED. Cutis marmorata telangiectatica congenita with multiple congenital anomalies. Arch Dermatol 1986;122:1060–1.
Ben-Amitai D, Merlob P, Metzker A. Cutis marmorata telangiectatica congenita and hypospadias: report of 4 cases. J Am Acad Dermatol 2001;45:131–2.
Powell ST, Su WPD. Cutis marmorata telangiectatica congenita: a report of 9 cases and review of the literature. Cutis 1984;34:305–12.
Torrielo HV, Graff RG, Florentine MF, Lacina S, Moore WD. Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome? Am J Med Genet 1988:29:269–76.
Bork K, Pfeifle J. Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams-Oliver syndrome. Br J Dermatol 1992:127:160–3.
Dyall-Smith D, Ramsden A, Laurie S. Adams-Oliver syndrome: aplasia cutis congenita, terminal transverse limb defects and cutis marmorata telangiectatica congenita. Australas J Dermatol 1994;35:19–22.
Bjornsdottir US, Laxdal T, Bjornsson J. Cutis marmorata telangiectatica congenita with terminal transverse limb defects. Acta Paediatr Scand 1988;77:780–2.
Mempel M, Abeck D, Lange I, et al. The wide spectrum of clinical expression in Adams-Oliver syndrome. A report of two cases. Br J Dermatol 1999;140:1157–60.
Schultz RB, Kocoshis S. Cutis marmorata telangiectatica congenita and neonatal ascites. J Pediatr 1979;95:157.
Spraker MK, Stack C, Esterly NB. Congenital generalized fibromatosis: a review of the literature and report of a case associated with porencephaly, hemiatrophy, and cutis marmorata telangiectatica congenita. J Am Acad Dermatol 1984;10:365–71.
Nicholls DSH, Harper JI. Cutis marmorata tetangiectatica congenita with soft-tissue herniations on the lower legs. Clin Exp Dermatol 1989;14:369–70.
Freund E. Diffuse genuine phlebectasia. Arch Surg 1936;33:113–21.
Shields JA, Shields CL, Koller HP, Federman JL, Koblenzer P, Barbera LS. Cutis marmorata telangiectatica congenita associated with bilateral congenital retinal detachment. Retina 1990;10:135–9.
Pendergast SD, Trese MT, Shastry BS. Ocular findings in cutis marmorata telangiectatica congenita. Bilateral exudative vitreoretinopathy. Retina 1997;17:306–9.
Kennedy C, Oranje AP, Keizer K, van den Heuvel MM, Catsman-Berrevoets CE. Cutis marmorata telangiectatica congenita. Int J Dermatol 1992;31:249–52.
Pehr K, Moroz B. Cutis marmorata telangiectatica congenita: long-term follow-up, review of the literature and report of a case in conjunction with congenital hypothyroidism. Pediatr Dermatol 1993;10:6–11.
O’Toole EA, Deasy P, Watson R. Cutis marmorata telangiectatica congenita associated with a double aortic arch. Pediatr Dermatol 1995;12:348–50.
Morgan JM, Naisby GP, Carmichael AJ. Cutis marmorata telangiectatica congenita with hypoplasia of the right iliac and femoral veins. Br J Dermatol 1997;137:119–22.
Gruppo RA, DeGrauw TJ, Palasis S, Kalinyak KA, Bofinger MK. Strokes, cutis marmorata telangiectatica congenita, and factor V Leiden. Pediatr Neurol 1998;18:342–5.
Chen CP, Chen HC, Liu FF, et al. Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascites. Br J Dermatol 1997;136:267–71.
Lentner A, Bohler U, Wittkopf-Baumann C, Younossi H, Grussendorf-Conen EI. Schmerzhafte Cutis marmorata teleangiectatica congenita. Hautarzt 1992;43:657–60.
Lingier P, Munck D, Godart S. Cutis marmorata telangiectatica congenita. A propos de quatre nouveaux cas. Phlebologie 1992;45:489–96.
Bormann G, Wohlrab J, Fisher M, Marsch WC. Cutis marmorata telangiectatica congenita: laser Doppler fluxmetry evidence for a functional nervous defect. Pediatr Dermatol 2001;18:110–3.
Fitzsimmons JS, Starks M. Cutis marmorata telangiectatica congenita or congenital generalized phlebectasia. Arch Dis Child 1970;45:724–6.
Atherton DJ. Naevi and other developmental defects. In: Champion RH, Burton JL, Ebling FJG eds. Textbook of Dermatology, 5th ed., Oxford, Blackwell Scientific, 1992:445–526.
Greist MC, Probst E. Cutis marmorata telangiectatica congenita on neonatal lupus. Arch Dermatol 1980;116:1102–3.
Caffascosa JM, Ribera M, Bielsa I, Coroleu W, Ferrandiz C. Cutis marmorata telangiectatica congenita or neonatal lupus? Pediatr Dermatol 1996;13:230–2.
Rupprecht R, Hundeiker M. Cutis marmorata teleangiectatica congenita. Wichtige Aspekte fur die dermatologisches Praxis. Hautarzt 1997;48:21–5.
Barsky SH, Rosen S, Geer DE, et al. The nature and evolution of port wine stains: a computer assisted study. J Invest Dermatol 1980;74:154–7. P
Hidano A, Purwoko R, Jitsukawa K. Statistical survey of skin changes in Japanese neonates. Pediatr Dermatol 1986;3:140–4.
Leung AKC, Telmesani AMA. Salmon patches in Caucasian children. Pediatr Dermatol 1989;6:185–7.
Nanda A, Kaur S, Bhakoo ON, et al. Survey of cutaneous lesions in Indian newborns. Pediatr Dermatol 1989;6:39–42.
Rivers JK, Fredericksen PC, Dibdin C. A prevalence survey of dermatoses in the Australian neonate. J Am Acad Dermatol 1990;23:77–81.
Tay YK, Morelli J, Weston WL. Inflammatory nuchal-occipital port-wine stains. J Am Acad Dermatol 1996;35:811–3.
Bonifazi E, Mazzota F. Inflammatory nuchal-occipital port-wine stains. J Am Acad Dermatol 1998;38:130.
Hatzis J, Kostakis P, Tosca A, et al. Nuchal nevus flammeus as a skin marker of prognosis in alopecia areata. Dermatologica 1988;177:149–51.
Metzker A, Shamir R. Butterflay-shaped mark: a variant form of nevus flammeus simplex. Pediatrics 1990;85:1069–71.
Patrizi A, Neri I, Orlandi C, Marini R. Sacral medial telangiectatic vascular nevus: a study of 43 children. Dermatology 1996;192:301–6.
Ben-Amital D, Davidson S, Schwartz M, et al. Sacral nevus flammeus simplex: the role of imaging. Pediatr Dermatol 2000;17:469–71.
Alper JG, Holmes, LB. The incidence and significance of birthmarks in a cohort of 4641 newborns. Pediatr Dermatol 1983;1:58–66.
Jacobs AH, Walton RG. The incidence of birthmarks in the neonate. Pediatrics 1976;58:218–22.
Finley JL, Noe JM, Arndt KA, et al. Port-wine stains: morphological variations and developmental lesions. Arch Dermatol 1984;120:1453–5.
Adams BB, Lucky AW. Acquired port-wine stains and antecedent trauma: case report and review of the literature. Arch Dermatol 2000;136:897–9.
Mills CM, Lanigan SW, Hughes J, Anstey AV. Demographic study of port wine stain patients attending a laser clinic: family history, prevalence of naevus anemicus and results of prior treatment. Clin Exp Dermatol 1997;22:166–8.
Hamm H. Harpple R. Naevus vascularis mixtus. Hautarzt 1986;37:388–92.
Enjolras O, Riche MC, Merland JJ. Facial port-wine stains and Sturge-Weber syndrome. Pediatrics 1985;76:48–51.
Stevenson RF, Morin JD. Ocular findings in nevus flammeus. Can J Ophthalmol 1975;10:136–9.
Stevenson RF, Thompson HG, Morin JD. Unrecognized ocular problems associated wim port-wine stains of the face in children. Can Med Assoc J 1974;111:953–4.
Witschel H, Font RL. Hemangioma of the choroid: a clinicopathological study of 7/ 1 cases and a review of the literature. Surv Ophthalmol 1976;20:415–31.
Uram M, Zubillaga C. The cutaneous manifestations of Sturge-Weber syndrome. J Clin Neuroophthalmol 1982;2:145–8.
Jacobs AH. Sturge-Weber syndrome without port-wine nevus. Pediatrics 1977; 60:785–6
Andriola M, Stolfii J. Sturge-Weber syndrome: report of an atypical case. Am J Dis Child 1972;123:507–10.
Crosley CJ, Binet EF. Sturge-Weber syndrome: presentation as a focal seizure without nevus flammeus. Clin Pediatr 1978;17:606–9.
Bebin EM, Gomer MR. The intelligence and social achievement of patients with unilateral and bihemispheric Sturge-Weber syndrome. J Child Neurol 1988;3:181–90.
Royle HE, Lapp R, Ferrara ED. The Sturge-Weber syndrome. Oral Surg Oral Med Oral Pathol 1966;22:490–7.
Cosman B. Clinical experience in the laser therapy of port-wine stains. Lasers Surg Med 1980;1:133–52.
Harper PS. Sturge-Weber syndrome with Klippel-Trenaunay syndrome. Birth Defects 1971;7:314.
Schofield D, Zaatari GS, Gay BB. Klippel-Trenaunay and Sturge-Weber syndromes with renal hemangioma and double inferior vena cava. J Urol 1986; 136:442–5.
Klippel M, Trenaunay P. Du noevus variqueux osteohypertrophique. Arch Gen Med 1900;3:641–72.
Parkes Weber F. Angioma formation in connection with hypertrophy of limbs and hemi-hypertrophy. Br J Dermatol 1907;19:231–5.
Adam JS, Cunliffe WJ. The Klippel-Trenaunay-Weber syndrome presenting with cutaneous bleeding. Acta Derm Venereol 1981;62:176–7.
Baskerville PA, Ackroyd JS, Thomas ML, et al. The Klippel-Trenaunay syndrome: clinical, radiological and haemodynamic features and management. Br J Surg 1985;72:232–6.
Phillips GN, Gordon DH, Mortin EC, et al. The Klippel-Trenaunay syndrome: clinical and radiological aspects. Radiology 1978;128:429–34.
Viljoen D, Saxe N, Peran J, et al. The cutaneous manifestations of the Klippel-Trenaunay-Weber syndrome. Clin Exp Dermatol 1987;12:12–17.
Toda K. A new type of phacomatosis pigmentovascularis (Ota). Jpn J Dermatol 1966;76:47–51.
Hasegawa Y, Yasuhara M. A variant of phakomatosis pigmentovascularis. Sin Res (Osaka) 1979;21:178–86.
Hasegawa Y, Yasuhara M. Phakomatosis pigmentovascularis type IVa. Arch Dermatol 1985;121:651–55.
Noriega Sanchez A, Markand ON, Herndon JH. Oculocutaneous melanosis associated with the SturgeWeber syndrome. Neurology 1972;22:256–62.
Furukawa T, Igata A, Toyokura Y, et al. Sturge-Weber and Klippel-Trenaunay syndrome with nevus de Ota and Ito. Arch Dermatol 1970;102:640–5.
Sigg C, Pelloni F. Oligosymptomatic form of Klippel-Trenaunay-Weber syndrome associated with giant nevus spilus. Arch Dermatol 1989;125:1284–5.
Guiglia MC, Prendiville JS. Multiple granular cell tumors associated with giant speckled lentiginous nevus and nevus flammeus in a child. J Am Acad Dermatol 1991;24:359–63.
Libow LF. Phakomatosis pigmentovascularis type Mo. J Am Acad Dermatol 1993; 29:305–7.
Smoller BR, Rosen S. Port wine stains: a disease of altered neural modulation of blood vessels? Arch Dermatol 1986;122:177–9.
Kissel P, Dureux JB. Cobb syndrome. Cutaneo-meningospinal angiomatosis. In: Bruyn GW, Vinken PJ, eds. Handbook of Clinical Neurology. New York, North Holland Publishing, 1972:429–45.
Archer DB, Deutman A, Ernest JT, et al. Arteriovenous communications of the retina. Am J Ophthalmol 1973.75:274–91
Ward JB, Kotz NNK. Combined phakomatoses: a case report of Sturge-Weber and Wyburn-Mason syndrome occurring in the same individual. Ann Ophthalmol 1983;15:1112–6.
Clark RD, Donnai D, Rogers J, Cooper J, Bardaitser M. Proteus syndrome: an expanded phenotype. Am J Med Genet 1987;27:99–117.
Samlaska CP, Levin SW, James WD, Benson PM, Walrer JC, Perlik PC. Proteus syndrome. Arch Dermatol 1989;125:1109–14.
Plotz SG, Abeck D, Plotz W, Ring J. Proteus syndrome with widespread portwine stain naevus. Br J Dermatol 1998;139:1060–3.
Freeman MVR, Williams DW, Schimke RN, et al. Roberts syndrome. Clin Genet 1974:5:1–16.
Ashinoff R, Geronemus RG. Thrombocytopenia-absent radii syndrome and lack of response to the pulsed dye laser. Arch Dermatol 1990;126:1520–1.
Horton WA, Wong V, Eldridge R. Von Hippel-Lindau disease. Clinical and pathological manifestations in nine families with 50 affected members. Arch Intern Med 1976;136:769–77.
Filippi G, McKusick VA. The Beckwith-Wiedmann syndrome (the exophthalmos-macroglossia-gigantism syndrome): report of two cases and review of the literature. Medicine 1970;49:279–98.
Rubinstein JH, Taybi H. Broad thumbs and toes and facial abnormalities. Am J Dis Child 1963;105:588–608.
Allen HB, Parlette HL. Coat’s disease: a condition that may mimic Sturge-Weber syndrome. Arch Dermatol 1973;108:413–5.
Hagiwara K, Khaskhely NM, Uezato H, Nonaka S. Mast cell “densities” in vascular proliferations: a preliminary study of pyogenic granuloma, portwine stain, cavernous hemangioma, cherry angioma, Kaposi’ s sarcoma, and malignant hemangioendothelioma. J Dermatol 1999:26:577–86.
Klapman MH, Yao JF. Thickening and nodules in port-wine stains. J Am Acad Dermatol 2001;44:300–2.
Swerlick RA, Cooper PH. Pyogenic granuloma (lobular capillary hemangioma) within port-wine stains. J Am Acad Dermatol 1983;8:627–30.
Lee JB, Kim M, Lee SC, Won YH. Granuloma pyogenicum arising in an arteriovenous hemangioma associated with a port-wine stain. Br J Dermatol 2000;143:669–71.
Katta R, Bickle K, Hwang L. Pyogenic granuloma arising in port-wine stain during pregnancy. Br J Dermatol 2001;144:644–5.
Kim TH, Choi EH, Ahn SK, Lee SH. Vascular tumors arising in port-wine stains: two cases of pyogenic granuloma and a case of acquired tufted angioma. J Dermatol 1999;26:813–6.
Burg G. Collision dermatosis: angiolymphoid hyperplasia with eosinophilia developing within a congenital port wine nevus. Dermatology 1993;187:293–5.
Sagi E, Aram H, Peled IJ. Basal cell carcinoma developing in a nevus flammeus. Cutis 1984;33:311–2.
Lo JS, Sgouros GN , Mohs PE, Snow SIN . basal cen carcinoma within a nevus fldmmmmmmeUS. RRepui t oof a case. Int J Dermatol 1991;30:725–6.
Shah M, Lewis FM, Palmer IR. Three cases of multiple basal cell carcinoma arising in port-wine stains previously treated with thorium X. Br J Dermatol 1996;135:861–2.
Wharton SM, Cole RP. Basal cell carcinoma in port wine stains. Br J Plast Surg 2001;54:156–8.
Rosen S, Smoller BR. Port-wine stains: a new hypothesis. J Am Acad Dermatol 1987;17: 14–bl
Mulliken JB, Glowacki J. Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg 1982;69:412–22.
Braverman IM, Ken-Yen A. Ultrastructure and three-dimensional reconstruction of several macular and papular telangectasias. J Invest Dermatol 1983;81:489–97.
Finley JL, Clark RAF, Colvin RB. Immunofluorescent staining with antibodies to factor VIII, fibronectin, and collagenous basement membrane protein in normal human skin and port-wine stains. Arch Dermatol 1982;118:971–5.
Neumann R, Leonhartsberger H, Knobler R, Hönigsmann H. Immunohistochemistry of port-wine stains and normal skin with endothelium-specific antibodies PAL-E, anti-ICAM-1, anti-ELAM-1, and antifactor VIIIrAg. Arch Dermatol 1994;130:879–83.
Ashinoff R, Geronemus RG. Flashlamp-pumped pulsed dye laser for port-wine stains in infancy: earlier versus later treatment. J Am Acad Dermatol 1991; 24:467–72.
Dover JS, Geronemus RG, Stern RS, O’Hare D, Arndt KA. Dye laser treatment of port-wine stains: comparison of the continuous-wave dye laser with a robotized scanning device and the pulsed dye laser. J Am Acad Dermatol 1995;32:237–40.
Garden JM, Polla LL, Tan OT. The treatment of port-wine stains by the pulsed dye laser. Arch Dermatol 1988;124:889–96.
Cliff S, Misch K. Treatment of mature port wine stains with the PhotoDerm VL. J Cutan Laser Ther 1999;1:101–4.
Scherer K, Lorenz S, Wimmershoff M, Landthaler M, Hohenleutner U. Both the flashlamp-pumped dye laser and the long-pulsed tunable dye laser can improve results in port-wine stain therapy. Br J Dermatol 2001;145:79–84.
Del Pozo J, Fonseca E. Port-wine stain nodules in the adult: report of 20 cases treated by CO2 laser vaporization. Dermatol Surg 2001;27:699–702.
Nguyen CM, Yohn JJ, Huff C, Weston WL, Morelli JG. Facial port wine stains in childhood: prediction of the rate of improvement as a function of the age of the patient, size and location of the port wine stain and the number of treatments with the pulsed dye (585 nm) laser. Br J Dermatol 1998;138:821–5.
Renfro L, Geronemus RG. Anatomical differences of port-wine stains in response to treatment with the pulsed dye laser. Arch Dermatol 1993;129:182–8.
Troilius A, Svendsen G, Ljunggren B. Ultrasond investigation of port wine stains. Acta Derm Venereol 2000;80 196–9.
Eubanks LE, McBurney EI. Videomicroscopy of port-wine stains. Correlation of location and depth of lesion. J Am Acad Dermatol 2001;44:948–51.
Seukeran DC, Collins P, Sheehan-Dare RA. Adverse reactions following pulsed tunable dye laser treatment of port wine stains in 701 patients. Br J Dermatol 1997;136:725–9.
Gaston DA, Clark DP. Facial hypertrophic scarring from pulsed dye laser. Dermnatol Surg 1998;24:523–5.
Ozluer SM, Barlow RI. Partial re-emergence of a port-wine stain following successful treatment with flashlamp-pumped dye laser. Clin Exp Dermatol 2001;26:37–9.
Michel S, Landthaler M, Hohenleutner U. Recurrence of port-wine stains after treatment with the flashlamp-pumped pulsed dye laser. Br J Dermatol 2000;143:1230–4.
Imperial R, Helwig EB. Verrucous hemangioma. A clinicopathologic study of 21 cases. Arch Dermatol 1967;96:247–53.
Loria PR, Derbes VJ, Krafchuk JD. Keratotic hemangiomas. Arch Dermatol 1958; 77:216–9.
De Dulanto F, Moreno MA, Martinez FC, Naranjo R. Angioqueratomas negros solitarios y hemangiomas verrugosos. Problemas y transcendencia del diagnostico diferencial con los melanomas malignos. Actas Dermosifiliogr 1975;66:376–86.
De Souza EM, Turini MA, Oliveira TC. Hemangioma verrucoso (acrohemangioma verrucoso neviforme). Med Cut Ibero Lat Am 1981;9:217–20.
Klein JA, Barr RJ. Verrucous hemangioma. Pediatr Dermatol 1985;2:191–3.
Colonna SM, Rotoli M, Aloi FG. Angioma verrucoso. A proposito di due casi clinici. G Ital Dermatol Venereol 1987;122:309–12.
Puig L, Llistosella E, Moreno A, de Moragas JM. Verrucous hemangioma. J Dermatol Surg Oncol 1987;13:1089–92.
Rossi A, Bozzi M, Barra E. Verrucous hemangioma and angiokeratoma circumscriptum: clinical and histologic differential characteristics. J Dermatol Surg Oncol 1989;15:88–91.
Cruces MJ, de la Tone C. Multiple eruptive verrucous hemangiomas: a variant of multiple hemangiomatosis. Dermatologica 1985;171:106–11.
Niechajev IA, Sternby NH. Cutaneous keratotic hemangioma. Scand J Plast Reconstr Surg 1983;17:153–4.
Gupta PK, Sharma DC, Kumwat DC, Bomb BS. Kasabach-Merritt syndrome with verrucous hemangiomata. J Assoc Physicians India 1993;41:612.
Chan JKC, Tsang WYW, Calonje E, Fletcher CDM. Verrucous hemangioma. A distinct but neglected variant of cutaneous hemangioma. Int J Surg Pathol 1995; 2:171–6.
Wong DS, Hunt SJ, Inserra DW, Abell E. Unilateral keratotic vascular lesion on the leg. Verrucous hemangioma. Arch Dermatol 1996;132:705.
Kawaguchi H, Kawaguchi T, Ishii N, Nakajima H, Ichiyama S. Verrucous hemangioma. Acta Derm Venereol 1997;77:405–6.
Tan YY, Seah CS, Tan PH. Verrucous hemangioma—a case report. Ann Acad Med Singapore 1998;27:255–7.
Jucgla A, Servitge O, Moreno A. Hemangioma verrucoso: estudio clinicopatol6gico de 10 casos [Abstract]. Actas Dermosifiliogr 1998;89:405–6.
Wentscher U, Happle R. Linear verrucous hemangioma. J Am Acad Dermatol 2000;42:516–8.
Calduch L, Ortega C, Navarro V, Martinez E, Molina I, Jorda E. Verrucous hemangioma: report of two cases and review of the literature. Pediatr Dermatol 2000;17:213–7.
Mankani MH, Dufresne CR. Verrucous malformations: their presentation and management. Ann Plast Surg 2000;45:31–6.
Rupani AB, Madiwale CV, Vaideeswar P. Images in pathology: verrucous haemangioma. J Postgrad Med 2000 46:132–3.
Kohda H, Narisawa Y. Digital verrucous fibroangioma: a new variant of verrucous hemangioma. Acta Derm Venereol 1992;72:303–4.
Newton JH, McGibbon DH. The treatment of multiple angiokeratomata with argon laser. Clin Exp Dermatol 1987;12:23–5.
Boon LM, Mulliken JB, Vikkula M, et al. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. Hum Mol Genet 1994;3:1583–7.
Mounayer C, Wassef M, Enjolras O, Boukobza M, Mulliken JB. Facial “glomangiomas”: large venous malformations with glomus cells. J Am Acad Dermatol 2001;45:239–45.
Boon LM, Brouillard P, Irrthum A, et al. A gene for inherited cutaneous venous anomalies (“glomangiomas”) localizes to chromosome 1p21–22. Am J Hum Genet 1999;65:125–33.
Kern S, Niemeyer C, Darge K, Merz C, Laubenberger J, Uhl M. Differential ofvascularbirthmarks by MR imaging. An investigation of hemangiomas, venous and lymphatic malformations. Acta Radiol 2000;41:453–7.
Boyd JB, Mulliken JB, Kaban LB, Upton J III, Murray JE. Skeletal changes associated with vascular malformations. Plast Reconstr Surg 1984;74:789–97.
Enjolras O, Ciabrini D, Mazoyer E, Laurian C, Herbreteau D. Extensive pure venous malformations in the upper or lower limb: a review of 27 cases. J Am Acad Dermatol 1997;36:219–25.
Bean WB. Blue rubber bleb nevi of the skin and gastrointestinal tract. In: Vascular Spiders and Related Lesions of the Skin. Springfield, MO, CC Thomas, 1958:178–85.
Berlyne GM, Berlyne N. Anaemia due to “blue rubber bleb” naevus disease. Lancet 1960;2:1275–7.
Munkvad M. Blue rubber bleb nevus syndrome. Dermatologica 1983;167;307–9.
Walshe MM, Evans CD, Warin RP. Blue rubber bleb naevus. BMJ 1966; 2:931–2.
Baker AL, Kahn PC, Binder SC, et al. Gastrointestinal bleeding due to blue rubber bleb nevus syndrome. Gastroenterology 1971;61:530–4.
McCauley RGK, Leonidas JC, Bartoshesky LE. Blue rubber bleb nevus syndrome. Radiology 1979:133:375–7.
Olsen TG, Milroy SK, Goldman L, et al. Laser surgery for blue rubber bleb nevus. Arch Dermatol 1979;115:81–2.
Baiocco FA, Gamoletti R, Negri A, et al. Blue rubber bleb nevus syndrome: a case with predominant ENT localization. J Laryngol Otol 1984;98:317–9.
McCarthy JC, Goldberg MJ, Zimbler S. Orthopedic dysfunction in the blue rubber bleb nevus syndrome. J Bone Joint Surg 1982;64A:280–3.
Rennie JG, Shortland JR, Mahood JM, et al. Periodic exophthalmos associated with blue rubber bleb nevus syndrome. Br J Ophthalmol 1982;66:594–8.
Satya-Murti S, Navada S, Eames F. Central nervous system involvement in blue rubber bleb nevus syndrome. Arch Neurol 1986;43:1184–6.
Sakurane HF, Sugai T, Saito T. The association of blue rubber bleb nevus and Maffucci’s syndrome. Arch Dermatol 1967;95:28–36.
Maffucci A. Di un caso di encondroma ed angioma multiple: contribuzione alla genesi embrionale dei tumori. Mov Med Chir Nap 1891;13:399–412.
Tilsley DA, Burden PW. A case of Maffucci’s syndrome. Br J Dermatol 1981;105:331–6.
Lewis RJ, Ketcham AS. Maffucci’s syndrome: functional and neoplastic significance: case report and review of the literature. J Bone Joint Surg 1973; 55A:1465–79.
Bean WB. Dyschondroplasia and hemangiomata (Maffucci’s syndrome). II. Arch Intern Med 1958;102:544–50.
Suringa DWR, Ackerman AB. Cutaneous lymphangiomas with dyschondroplasia (Maffucci’s syndrome): a unique variant of an unusual syndrome. Arch Dermatol 1970;191:472–4.
Johnson JL, Webster Jr, Sippy HI. Maffucci’s syndrome (dyschondroplasia with hemangiomas). Am J Med 1960;28:864–6.
Nardell SG. 011ier’s disease: dyschondroplasia. BMJ 1950;2:555–7.
Klippel M, Trenaunay P. Du noevus variqueux osteohypertophique. Arch Gen Med 1900;3:641–72.
Parkes Weber F. Angioma formation in connection with hypertrophy of limbs and hemi-hypertrophy. Br J Dermatol 1907;19:231–5.
Lindenauer SM. Klippel-Trenaunay syndrome. Ann Surg 1965;162:303–10.
Cosman B. Clinical experience in the laser therapy of port-wine stains. Lasers Sure Med 1980:1:133–52.
Harper PS. Sturge-Weber syndrome with Klippel-Tranaunay syndrome. Birth Defects 1971:7:314.
Schofield D, Zaatari GS, Gay BB. Klippel-Trenaunay and Sturge-Weber syndromes with renal hemaneioma and double inferior vena cava. J Urol 1986:136:442–5.
Adam JS, Cunliffe WJ. The Klippel-Trenaunay-Weber syndrome presenting with cutaneous bleeding. Acta Dermm Venereol 1981;62:176–7.
Baskerville PA, Ackroyd JS, Thomas ML, et al. The Klippel-Trenaunay syndrome: clinical, radiological and haemodynamic features and management. Br J Surg 1985;72:232–6.
Phillips GN, Gordon DH, Mortin EC, et al. The Klippel-Trenaunay syndrome: clinical and radiological aspects. Radiology 1978;128:429–34.
Viljoen D, Saxe N, Peran J, et al. The cutaneous manifestations of the Klippel-Trenaunay-Weber syndrome. Clin Exp Dermatol 1987;12:12–7.
Servelle M. Klipnel-Trenaunav syndrome. Ann Suurg 1985;201.365–76
Young AE, Ackroyd J, Baskerville P. Combined vascular malformations. In: Mulliken JB, Young AE, eds. Vascular Birthmarks. Hemangiomas and malformations. Philadelphia, WB Saunders, 1988:247–74.
Germain DP. Co-occurrence and contribution of Fabry disease and Klippel-Trenaunay-Weber syndrome to a patient with atypical skin lesions. Clin Genet 2001;60:63–7.
Gorham LW, Wright AW, Shultz HH, et al. Disappearing bones: a rare form of massive osteolysis. Am J Med 1954;17:674–82.
Frost JF, Caplan RM. Cutaneous haemangiomas and disappearing bones with a review of cutaneovisceral haemangiomatosis. Arch Dermatol 1965;92:501–8.
Gellis SS, Feingold M. Hemangiomas with osteolysis (Gorham’s disease: vanishing bone disease). Am J Dis Child 1978;132:715–6.
Mendez AA, Keret D, Robertson W, et al. Massive osteolysis of the femur (Gorham’ s disease): a case report and review of the literature. J Pediatr Orthop 1989;9:604–8.
Haferkamp O. Uber das Syndrome generalisierte maligne Haemangiomatosis mit Osteolysis. Krebforsch 1962;64:418–26.
Bannayan GA. Lipomatosis, angiomatosis, and macrocephalia: a previously undescribed congenital syndrome. Arch Pathol 1971;92:1–5.
Higginbottom MC, Schultz P. The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. Pediatrics 1982;69:632–4.
Miles HR, Zonana J, MacFarland J. Macrocephaly with hamartomas: Bannayan-Zonana syndrome. Am J Med Genet 1984;19:225–34.
Zonana J, Rimoin DL, Davis DC. Macrocephaly with multiple lipomas and hemangiomas. J Pediatr 1976;89:600–3.
Klein JA, Barr RJ. Bannayan-Zonana syndrome associated with lymphangiomatous lesions. Pediatr Dermatol 1990;7:48–53.
Saul RA, Stevenson RE, Bley R. Mental retardation in the Bannayan syndrome. Pediatrics 1982;69:642–4.
Riley HD, Smith WR. Macrocephaly, pseudopapilloedema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics 1960;26:293–300.
Ruvalcaba RHA, Myhre S, Smith DW. Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia. Clin Genet 1980;18:413–6.
Halal F. Male to male transmission of cerebral gigantism. Am J Med Genet 1982;12:411–9.
Halal F. Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia. Am J Med Genet 1983;15:161.
Cohen MM Jr. The large-for-gestational-age (LGA) infant in dysmorphic perspective. In: Willey AM, Carter TP, Kelly S, Porter IH, eds. Clinical Genetics: Problems in Diagnosis and Counseling. New York, Academic,1982:153–69.
DiLiberti JH, Weleber RG, Budden S. Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations. Am J Med Genet 1983;15:491–5.
DiLiberti JH, D’ Agostino AN, Ruvalcaba RHA, Schimschock KR. A new lipid storage myopathy observed in individuals with the Ruvalcaba-Myhre-Smith syndrome. Am J Med Genet 1984;18:163–7.
Gretzula JC, Hevia O, Schachner LS, et al. Ruvalcaba-Myhre-Smith syndrome. Pediatr Dermatol 1988;5:28–32.
Dvir M, Beer S, Aladjem M. Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema. Pediatrics 1988;81:287–90.
Cohen MM Jr. Bannayan-Riley-Ruvalcaba syndrome: renaming three formerly recognized syndromes as one etiologic entity. Am J Med Genet 1990;35:291.
Gorlin RS, Cohen MM, Leven LS. Bannayan-Riley-Ruvalcaba syndrome (Bannayan-Zonana syndrome, Ruvalcaba-Myhre, Riley-Smith syndrome). In: Gorlin RS, Cohen MM, Leven LS, eds. Syndromes of the Head and Neck. New York, Oxford University Press, 1990:336–8.
Gorlin RJ, Cohen MM Jr, Condon LM, Burke BA. Bannayan-Riley-Ruvalcaba syndrome. Am J Med Genet 1992;44:307–14.
Fargnoli MC, Orlow SJ, Semel-Concepcion J, Bolognia JL. Clinicopathologic findings in the BannayanRiley-Ruvalcaba syndrome. Arch Dermatol 1996;132:1214–8.
Steinway DM, Fretzin DF. Acquired zosteriform cavernous hemangiomas: brief clinical observations. Arch Dermatol 1977;113:848–9.
Wilkin JK. Unilateral dermatomal cavernous hemangiomatosis. Dermatologica 1980;161:347–54.
Hurst J, Baraitser M. Hereditary neurocutaneous angiomatous malformations: autosomal dominant transmission in two families. Clin Genet 1988;33:44–8.
Hersh JH, Waterfill D, Rutledge J, et al. Sternal malformation/vascular dysplasia association. Am J Hum Genet 1985;21:177–84.
Hall BD, deLorimier A, Foster LH. Brief clinical report: a new syndrome of hemangiomatous branchial clefts, lip pseudoclefts and unusual facial appearance. Am J Med Genet 1983;14:135–8.
Goldberg NS, Hebert AA, Esterly NB. Sacral hemangiomas and multiple congenital anomalies. Arch Dermatol 1986;122:684–7.
Goldberg RE, Pheasant TR, Shields JA. Cavernous hemangioma of the retina: a four generation pedigree with neurocutaneous manifestations and an example of bilateral retinal involvement. Arch Ophthalmol 1979;97:2321–4.
Pasyk KA, Argenta LC, Erikson RP. Familial vascular malformations: report of 25 members of one family. Clin Genet 1984;24:221–7.
Rice J, Fisher D. Blue rubber-bleb nevus syndrome. Generalized cavernous hemangiomas or venous hamartoma with medulloblastoma of the cerebellum. Case report and review of the literature. Arch Dermatol 1962;86:503–11.
Fretzin DF, Potter B. Blue rubber bleb nevus. Arch Intern Med 1965;116:924–9.
Hagood MF, Gathright JB Jr. Hemangiomatosis of the skin and gastrointestinal tract: report of a case. Dis Colon Rectum 1975;18:141–6.
Rosenblum WI, Nakoneczna I, Konerding HS, Nochlin D, Ghatak NR. Multiple vascular malformation in the “blue rubber bleb naevus” syndrome. A case with aneurysm of vein of Galen and vascular lesions suggesting a link to the Weber-Osler-Rendu syndrome. Histopathology 1978;2:301–11.
Weiss SW, Enzinger FM. Spindle cell hemangioendothelioma: a low-grade angiosarcoma resembling a cavernous hemangioma and Kaposi’ s sarcoma. Am J Surg Pathol 1986;10:521–30.
Scott GA, Rosai J. Spindle cell hemangioendothelioma. Report of seven additional cases of a recently described vascular neoplasm. Am J Dermatopathol 1988;10:281–8.
Lawson JP, Scott G. Case report 602. Skeletal Radiol 1990;19:158–62.
Murakami J, Sarker AB, Teramoto N, Hore Y, Tagucmi K, Akagi T. Spindle cell hemangioendothelioma: a report of two cases. Acta Pathol Jpn 1993;43:529–34.
Pellegrini AE, Drake RD, Qualman SJ. Spindle cell hemangioendothelioma: a neoplasm associated with Maffucci’ s syndrome. J Cutan Pathol 1995;22:176–6.
Fukunaga M, Ushigome S, Nikaido T, Ishikawa E, Nakamori K. Spindle cell hemangioendothelioma: an immunohistochemical and flow cytometric study of six cases. Pathol Int 1995;45:589–95.
Hisaoka M, Koumo H, Aoki T, Hashimoto H. DNA flow cytometric and immunohistochemical analysis of proliferative activity in spindle cell haemangioendothelioma. Histopathology 1995;27:451–6.
Fanburg JC, Meis-Kindblom JM, Rosenberg AE. Multiple enchondromas associated with spindle cell hemangioendotheliomas: an overlooked variant of Maffucci’ s syndrome. Am J Surg Pathol 1995;19:1029–38.
Niechajev IA, Hansson LI. Maffucci’s syndrome. Scand J Plast Reconst Surg 1982;16:215–9.
Whimster J. The pathology of lymphangioma circumscriptum. Br J Dermatol 1976;94:473–86.
Flanagan BP, Helwig EB. Cutaneous lymphangioma. Arch Dermatol 1977;113:24–30.
Peachey RDG, Lim CC, Whimster JW. Lymphangioma of the skin: a review of 65 cases. Br J Dermatol 1970;83:519–27.
Russell B, Pridie RB. Lymphangioma circumscriptum with involvement of deep lymphatics. Br J Dermatol 1967;79:300.
Palmer LC, Strauch WG, Welton WA. Lymphangioma circumscriptum: a case with deep lymphatic involvement. Arch Dermatol 1978;114:394–6.
McAlvany JP, Jorizzo JL, Zanolli D, et al. Magnetic resonance imaging in the evaluation of lymphangioma circumscriptum. Arch Dermatol 1993;129:194–7.
Mordehai J, Kurzbart E, Shinhar D, Sagi A, Finaly R, Nares AJ. Lymphangioma circumscriptum. Pediatr Surg Int 1998;13:208–10.
Irvine AD, Sweeney L, Corbett JR. Lymphangioma circumscriptum associated with paravesical cystic retroperitoneal lymphangioma. Br J Dermatol 1996;134:1135–7.
Oyler RM, Davis DA, Woosley JT. Lymphangioma associated with Becker’ s nevus: a report of coincident hamartomas in a child. Pediatr Dermatol 1997;14:376–9.
Suringa DW, Ackerman AB. Cutaneous lymphangiomas with dyschondroplasia (Maffucci’ s syndrome). A unique variant of an unusual syndrome. Arch Dermatol 1970;101:472–4.
Shim JH, Lee DW, Cho BK. A case of Cobb syndrome associated with lymphangioma circumscriptum. Dermatology 1996;193:45–7.
Bauer BS, Kernahan DA, Hugo NE. Lymphangioma circumscriptum: a clinicopathologic review. Ann Plast Surg 1981;7:318–26.
Pearson JM, McWilliam L . Alight microscopical, immunohistochemical, and ultrastructural comparison of hemanaioma and lvmphangioma. Ultrastruct Pathol 1990;14:497–504.
Lymboussaki A, Partanen TA, Olofsson B, et al. Expression of the vascular endothelial growth factor C receptor VEGFR-3 in lymphatic endothelium of the skin and in vascular tumors. Am J Pathol 1998;153:395–403.
Folpe AL, Veikkola T, Valtola R, Weiss SW. Vascular endothelial growth factor receptor-3 (VEGFR-3): a marker of vascular tumors with presumed lymphatic differentiation, including Kaposi’ s sarcoma, kaposiform and Dabska-type hemangioendotheliomas, and a subset of angiosarcomas. Mod Pathol 2000;13:180–5.
0’ Cathail S, Rostom AY, Johnson ML. Successful control of lymphangioma circumscriptum by superficial X-rays. Br J Dermatol 1985;113:611–5.
King DT, Duffy DM, Hirose FM, Gurevitch AW. Lymphangiosarcoma arising from lymphangioma circumscriptum. Arch Dermatol 1979;115:969–72.
Landthaler M, Haina D, Waidelich W, Braun-Falco O. Behandlung zirkumskripter lymphangiome mit dem Argonlaser. Hautarzt 1982;33:266–70.
Bailin PL, Kantor GR, Wheeland RG. Carbon dioxide laser vaporization of lymphangioma circumscriptum. J Am Acad Dermatol 1986;14:257–62.
Eliezri YD, Sklar JA. Lymphangioma circumscriptum: review and evaluation of carbon dioxide laser vaporization. J Dermatol Surg Oncol 1988;14:357–64.
Haas AF, Narurkar VA. Recalcitrant breast lymphangioma circumscriptum treated by ultrapulse carbon dioxide laser. Dermatol Surg 1998;24:893–5.
Wimmershoff MB, Schreyer AG, Glaessl A, et al. Mixed capillary/lymphatic malformation with coexisting port-wine stain: treatment utilizing 3D MRI and CT-guided sclerotherapy. Dermatol Surg 2000;26:584–7.
Flannan BR, Helwig EB. Cutaneous lymphangioma. Arch Dermatol 1977:113:24–30.
Peachey RDG, Lim CC, Whimster JW. Lymphangioma of the skin: a review of 65 cases. Br J Dermatol 1970;83:519–27.
Harkins GA, Sabiston DC. Lymphangioma in infancy and childhood. Surgery 1960;47:811–22.
Suringa DWR, Ackerman AB. Cutaneous lymphangiomas with dyschondroplasia (Maffucci’ s syndrome): a unique variant of an unusual syndrome. Arch Dermatol 1970;191:472–4.
Bill AH, Sumner DS. A unified concept of lymphangioma and cystic hygroma. Surg Gynecol Obstet 1965;120:79–86.
Chervenak FA, Isaacson G, Blakemore KJ, et al. Fetal cystic hygroma cause and natural history. N Engl J Med 1983;309:822–5.
Russell B, Pridie RB. Lymphangioma circumscriptum with involvement of deep lymphatics. Br J Dermatol 1967;79:300.
Edwards JM, Peachey RDG, Kinmonth JB. Lymphangiography and surgery in lymphangioma of the skin. Br J Surg 1972;59:36–41.
Jordan PR, Sanderson KV, Wilson JSP. Surgical treatment of lymphangioma circumscriptum: a case report. Br J Plast Surg 1977;30:306–7.
Nanda Kumar H, Bhaskar Roa C, Kukreja R. Management of lymphangioma by cryoprobe: a case report. J Indian Dent Assoc 1982;54:25–7.
O’Cathial S, Rostom AY, Johnson ML. Successful control of lymphangioma circumscriptum by superficial x-rays. Br J Dermatol 1985;113:611–5.
Bailin PL, Kantor GR, Wheeland RG. Carbon dioxide laser vaporization of lymphangioma circumscriptum. J Am Acad Dermatol 1986;14:257–62.
Ogita S, Tsuto T, Tokiwa K, Takahashi T. Intracystic injection of OK-432. A new sclerosing therapy for cystic hygroma in children. Br J Surg 1987;74:690–1.
Romani P, Shah A. Lymphangiomatosis and immunohistochemical analysis of four cases. Am J Surg Pathol 1993;17:329–35
Singh Gomez C, Calonje E, Ferrar DW, Browse NL, Fletcher CDM. Lymphangiomatosis of the limbs. Clinicopathologic analysis of a series with a good prognosis. Am J Surg Pathol 1995;19:125–33.
Lauret P, Monconduit M, Sonlica J. Lymphangiomatose cutanée et osseuse disseminée avec coagulation intra-vasculaire disseminée. Ann Dermatol Venereol 1978;105:759–63.
Zukerberg LR, Nickoloff BJ, Weiss SW. Kaposiform hemangioendothelioma of infancy and childhood. An aggressive neoplasm associated with Kasabach-Merritt syndrome and lymphangiomatosis. Am J Surg Pathol 1993;17:321–8.
Mentzel T, Mazzoleni G, Dei Tos AP, Fletcher CD. Kaposiform hemangioendothelioma in adults. Clinicopathologic and immunohistochemical analysis of three cases. Am J Clin Pathol 1997;108:450–5.
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Sangüeza, O.P., Requena, L. (2003). Cutaneous Vascular Malformations. In: Pathology of Vascular Skin Lesions. Current Clinical Pathology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-360-6_5
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