Abstract
The relationships between the skeleton and the bone marrow tissue as resulting from anatomy, embryology and physiology, are so close that the idea of a physiopathological solidarity of the two structures is quite justified. Of course between the two systems, the osseous and the haemopoietic, the possibilities of mutual reaction are undoubtedly existent. This is justified on one hand by the anatomical substrate characterizing the bone in the various periods of life (in childhood, for example, every response is distinctly more animated) and on the other hand, by physiopathological conditions inherent to the haemopathy, whose manifestations may vary as to time of onset, seriousness and duration (Sansone and Mastragostino).
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References
Acun̂a, M.: Altérations radiologiques du squelette dans l’ictère hémolitique congénital. Bull. Soc. méd. Hôp. Paris 53, 1528–1535 (1937).
Alder, A.: Über konstitutionell bedingte Granulationsveränderungen der Leukocyten. Dtsch. Arcb. klin. Med. 183, 372–378 (1939).
——— Konstitutionell bedingte Granulationsveränderungen der Leukocyten und Knochenveränderungen. Schweiz. med. Wschr. 80, 1095–1098 (1950).
Almklov, J. R., A. E. Hansen and M. Schneider: Long bone involvement in sickle cell anemia. Pediatrics 5, 204–209 (1950).
Altmann, A.: Sickle cell anemia in South African-born European. Clin. Proc. 4, 1–10 (1945).
Banks, L. O., R. B. Scott and J. Simmons: Studies in sickle cell anemia; inheritance factor, including effect of interaction of genes for sicklemia and thalassemia. Amer. J. Dis. Child. 84, 601–608 (1952).
Baserga, A.: La malattia di Rietti-Greppi-Micheli. Progr. méd. (Paris) 10, 129–134 (1954).
Belloni, L., e P. Fornara: Istogenesi del cranio a spazzola nel morbo di Cooley. Minerva pediat. 7, 1638–1645 (1955).
Benassi, E., e A. Toti: Osservazioni sulle ossa rinvenute negli scavi della necropoli di Spina. Minerva fisioter. 2, 215–223 (1957).
Bernard, J., M. Dugas et M. Cotlenko: L’elliptocytose génotypique. A propos de dix observations personnelles. Ann. Méd. 54, 652–678 (1953).
——— E, Undritz, A. Bru, G. Mathe’ et J. Toulouse: Anomalie de Pelger homozygote chez l’homme. Sang 27, 819–824 (1956).
Biondetti, P.: Sul morbo di Cooley in soggetti adulti. Ann. Radiol. diagn. (Bologna) 25, 30–49 (1952).
Bishop, F. W.: Elliptical human erythrocytes. Arch. intern, Med. 14, 388 (1914).
Buchman, J.: Sickle cell disease simulating osteomyelitis. Bull. Hosp. J. Dis, (N.Y.) 10, 239–251 (1949).
Busacchi, V.: Esisteva il morbo di Cooley nel-l’America precolombiana ? Castalia 2, 125–129 (1946).
Gaffey, J.: Skeletal changes in chronic hemolytic anemias (erythroblastic anemia). Amer. J. Roentgenol. 37, 293–324 (1937).
——— Pediatric X-Ray diagnosis. Chicago: Ed. The Year Book 1950.
——— Cooley’s erythroblastic anemia; some skeletal findings in adolescents and young adults. Amer. J. Roentgenol. 65, 547–560 (1951).
——— Cooley’s anemia: a review of the roentgenographic findings in the skeleton. Amer. J. Roentgenol. 78, 381–391 (1957).
Caminopetros, J.: The sickle cell anomaly as a sign of Mediterranean anemia. Lancet 262, 687–693 (1952).
——— L’aspect radiologique des lésions osseuses de l’anémie erythroblastique infantile. Bull. Soc. méd. Hôp. Paris 3, 1442 (1953).
Carrington, H. T., A. D. Ferguson and R. B. Scott: Studies in sickle cell anemia. Bone involvement simulating aseptic necrosis. Amer. J. Dis. Child. 95, 157–163 (1958).
Carrol, D. S.: Roentgen manifestations of sickle cell disease. Sth. med. J. (Bgham, Ala.) 50, 1486–1490 (1957).
——— and J. W. Evans: Roentgen findings in sickle cell anemia. Radiology 53, 834–844 (1949).
Castagnari, G.: Intorno ad una particolare sindrome osteoporotica diffusa in un caso di anemia eritroblastica dell’infanzia. Bull. Sci. med. 1, 399–401 (1933).
——— La sindrome radiografica dell’anemia mediterranea o eritroblastica di tipo Cooley. Boll. Soc. ital. pediat. 3, 513–515 (1934).
——— e A. Toti: Il quadro radiologico osseo nel-l’ittero emolitico a resistenze globulari aumentate. Atti Accad. Sci. Ferrara 25, 33–34 (1947).
Cathala, J., P. Ducas et R. Abaza: Anémie splénique hémolytique et dystrophie cranienne. Bull. Soc. méd. Hôp. Paris 51, 1655–1661 (1935).
Charmot, G., J. Monfort, R. Raymond et E. Charmot: Les altérations osseuses dans l’anémie drépanocytaire chez l’enfant. Arch. franç. Pédiat. 16, 115–121 (1959).
Ciplea, A. G., et C. Ciorapciu: Anomalie leucocytaire Pelger-Huët homozygote humaine. Presse méd. 66, 554–555 (1958).
Coffey, J. D., and D. D. Salmon: Cooley’s erythroblastic anemia in Negro girl. J. Pediat. 34, 621–625 (1949).
Colarizi, A.: Ittero emolitico con alterazioni ossee tipo Cooley. Boll. Accad. med. Roma 68, 127–142 (1942).
——— Confronto fra le alterazioni ossee nel morbo di Cooley e nel morbo di Gaucher. Minerva pediat. 7, 1609–1610 (1955).
——— e I.Biddau: Anemie eritroblastiche splenomegaliche dell’infanzia. La malattia di Cooley. Haematologica 22, 351–431 (1940).
Consoli, G., C. Sandomenicoe A. Violane : A proposito di due osservazioni di morbo di Cooley in soggetti adulti. Sintesi 1, 369 (1957).
Cooley, T. B., and P. Lee: A series of cases of anemia with splenomegaly and peculiar bone changes. Trans. Amer. pediat. Soc. 37, 29 (1925).
——— E. R. Witwer and P. Lee: Anemia in children with splenomegaly and peculiar changes in the bones. Amer. J. Dis. Child. 34, 347–363 (1927).
Corcoran, W. J.: Erythroblastic anaemia, with report of case in boy 8 years old. Radiology 43, 373–375 (1944).
Dacie, J. V.: The hemolytic anaemias. London: Churchill 1954.
Danford, E. A., R. Marr and E. C. Elsey: Sickle cell anemia, with unusual bone changes. Amer. J. Roentgenol. 45, 223–226 (1941).
Deibert, K. R.: Roentgen changes in sickle cell anemia. Amer. J. Roentgenol. 82, 501–504 (1959).
DeMaestri, A., A. Pelizza e G. Villa Venzano : Rilievi radiologici nel morbo di Cooley e nel-l’ittero emolitico costituzionale. Minerva med. 50, 3611 (1959).
D’Eramo, N.: L’osteopatia emopatica. Recenti Progr. Med. 28, 442–467 (1960).
——— e G. De Gaetano : Le alterazioni ossee nelle emopatie. Roma: Universo 1957.
Diggs, L. W., H. N. Pulliam and J. C. King: Bone changes in sickle cell anemia. Sth. med. (Bgham, Ala.) 30, 249–259 (1937).
Dresbach, M.: Elliptical human red blood corpuscles. Science 19, 469 (1904).
Ducla-Soares, A., et F. Parreira: Anémie elliptocytique familiale. Etude de 3 cas personnels. Sang 29, 33–46 (1958).
Durando, E., e E. Grassi: L’iperostosi cranica basale nel quadro clinico e radiologico del-l’emopatia talassemica. Minerva pediat. 11, 905–909 (1959).
Falsetti, L, e I. Minutoli: SU di una rara manifestazione dell’anemia a cellule falciformi. Radiol. med. (Torino) 43, 750–755 (1957).
Falsetti, L.: Un carattere genotipico dell’anemia a cellule falciformi. Nunt. radiol. (Roma) 22, 885–892 (1956).
Ferrata, A., e E. Storti: Le malattie del sangue. Milano: Vallardi 1958.
Ferreri, L.: Il quadro radiologico del morbo di Cooley nell’adulto. Radiol. med. (Torino) 49, 710 (1953).
——— Studio radiologico delle alterazioni ossee in un caso di malattia drepanocitica. Radiologia (Roma) 13, 687–702 (1957).
Fricker-Alder, H.: Über einen neuen Fall von Alderscher Granulationsanomalie. Winterthur: P. G. Keller 1956.
Friedman, L. J.: Osseous changes in hemolytic icterus. Amer. J. Roentgenol. 20, 440–444 (1928).
Frongia, L.: Alterazioni bucco-dentarie nel morbo di Cooley. Rass. med. sarda 44, 293–306 (1942).
Frontali, G., e F. Rasi: L’eritroblastosi e l’emolisi nella malattia di Cooley e di Di Guglielmo. Arch. ital. Pediat. 7, 259–345 (1939).
Gänsslen, M.: Über hämolytischen Ikterus. Dtsch. Arch. klin. Med. 140, 210–226 (1922).
——— Der hämolytische Ikterus und hämolytische Konstitution. Klin. Wschr. 6, 929–933 (1927).
——— E. Zipperlen u. E. Schüz: Die hämolytische Konstitution. Dtsch. Arch. klin. Med. 146, 1–46 (1925).
Gardner, L. B.: Cooley’s erythroblastic anemia in 2 Chinese boys. J. Pediat. 31, 347–354 (1947).
Gasser, C.: Die hämolytischen Syndrome im Kindesalter. Stuttgart: Georg Thieme 1951.
Gatto, I.: L’ipoevolutismo nella malattia di Cooley. G. med. 3, 357–370 (1946).
——— Forme ed ereditarietà della thalassemia (microcarterocitosis). Policlin. infant. 16, 236–242 (1948).
——— Origine della thalassemia. Acta genet. (Basel) 8, 69–74 (1959).
——— e G. Puzzarella : Ulteriori ricerche in genetica sulla drepanocitosi. Pediatria (Napoli), 59, 789–798 (1951).
Gerrits, H. T., et A. de Vries: Quoted by Bernard et Coll.
Golding, J. S. R.: The bone changes in sickle cell anemia. Ann. Coll. Surg. England 19, 296–315 (1956).
Greenblatt, I. J., T. D. Cohn and H. L. Deutsch: Mediterranean target-oval cell syndrome in adult Chinese male. Ann. intern. Med. 24, 259–261 (1946).
Grignani, F., e E. Sulis: Morbo di Cooley e gravidanza. A proposito di una eccezionale osservazione. Minerva med. 51, 549–555 (1960).
Grinnan, A. G.: Roentgenologic bone changes in sickle cell and erythroblastic anemia report of nine cases. Amer. J. Roentgenol. 34, 297–309 (1935).
Günther, H.: Formprobleme an menschlichen Erythrocyten. Folia haemat. (Pavia) 35, 383–417 (1928).
Hamburg, A. E.: Skeleton changes in sickle cell anemia; report of an unusual case. J. Bone Jt Surg. 32, 893–900 (1950).
Hamperl, H., u. P. Weiss: Über die spongiöse Hyperostose an Schädeln aus Alt-Peru. Virchows Arch. path. Anat. 327, 629–642 (1955).
Hardin, A. S.: Sickle cell anemia; changes in the vessels and in the bones. Amer. J. Dis. Child. 54, 1045–1051 (1937).
Haverkamp-Begemann, N., and A. van Lockeren Campagne: Homozygous form of Pelger-Huët’s nuclear anomaly in man. Acta haemat. (Basel) 7, 295–303 (1952).
Heilmeyer, L.: Die Sphärocytose als Ausdruck einer pathologischen Funktion der Milz. Dtsch. Arch. klin. Med. 179, 292–306 (1936).
———, u. H. Begelmann : Blut und Blutkrankheiten. Berlin-Göttingen-Heidelberg: Springer 1951.
Henkin, W. A.: Collapse of vertebral bodies in sickle cell anemia. Amer. J. Roentgenol. 62, 395–401 (1949).
Hook, E. W., C. G. Campbell, H. S. Weens and G. R. Cooper: Salmonella osteomyelitis in patients with sickle cell anemia. New Engl. J. Med. 257, 403–407 (1957).
Huët, G. J.: Über eine bisher unbekannte familiäre Anomalie der Leukocyten. Klin. Wschr. 11, 1264–1266 (1932).
Ivy, R. E., and R. H. Howard: Sickle cell anemia with unusual bone changes. J. Pediat. 43, 312–315 (1953).
Jordans, G. H. W.: Familial granulation anomaly of leukocytes. Ned. T. Geneesk. 91, 1552–1555 (1947).
Kimmelstiel, P.: Vascular occlusion and ischemic infarction in sickle cell disease. Amer. J. med. Sci. 216, 11–19 (1948).
Kline, A. H., and G. H. Holman: Hereditary spherocytosis in the negro. Amer. J. Dis. Child. 94, 609–615 (1957).
Kokubo, Y.: Second family case of Pelger’s familial nuclear anomaly of leucocytes reported in Japan and further blood investigation of cases belonging to first family case. Tohoku J. exp. Med. 36, 1–16 (1939).
Lambrecht, K.: Die Elliptocytose (Ovalocytose) und ihre klinische Bedeutung. Ergebn. inn. Med. Kinderheilk. 55, 295–319 (1938).
Lanza, G.: Il morbo di Cooley nei suoi fondamentali aspetti anatomo-clinici ed etiopatogenetici. Arch. Med. mutual, (Koma) 12, 177–188 (1958).
Larizza, P.: Problemi aperti in tema di emopatia mediterranea. Minerva med. 49, 2181–2188 (1958).
Legant, O., and R. P. Ball: Sickle cell anemia in adults; roentgenographic findings. Radiology 51, 665–675 (1948).
Lehmann, H.: The sickle cell trait: not an essentially negro feature. Man 53, 9–16 (1953).
Leitner, S. I.: Panmyelopathie bei der Alderschen Anomalie. Schweiz. med. Wschr. 81, 1256–1257 (1951).
Liakka, V.: Über Höckerbildung in den Schädelknochen bei schweren Anämien der Kinder. Acta paediat. (Uppsala) 33, 104–114 (1945).
Litschgi, J. J.: Exhibit in Roentgen and hematological manifestations of the congenital hemolytic anemias. American Academy of Pediatrics Annual Meeting — Chicago, October 1959.
Macht, S. H., and P. W. Roman: The radiological changes in sickle cell anemia. Radiology 51, 697–707 (1948).
Maggioni, G., e A. Ascenzi: Morbo di Cooley. Roma: Abruzzini 1948.
Malhotra, R. P., and P. N. Chhuttani: Case of Cooley’s anemia. Indian med. Gaz. 79, 198–199 (1944).
Martoni, L.: A proposito dell’osservazione di una crisi di mieloaplasia eritroblastica nel decorso della malattia di Minkowski-Chauffard. Minerva med. 47, 215–220 (1956).
Middlemiss, J. H.: Sickle cell anemia. J. Fac. Radiol. (Lond.) 9, 16–24 (1958).
Moore, S.: Bone changes in sickle cell anemia with note on similar changes observed in skulls of ancient Mayan Indians. J. Mo. med. Ass. 26, 561–564 (1929).
Moseley, J. E.: Patterns of bone changes in the sickle cell states. J. Mt. Sinai Hosp. 26, 424–439 (1959).
———, and J. B. Manly: Aseptic necrosis of bone in sickle cell disease. Radiology 60, 656–665 (1953).
Munoz-Baratto, C.: La anomalia di Pelger. Atti VII. Congr. Int. Soc. Hemat. 2, 1621–1629 (1959).
Nachtsheim, H.: Die Pelger-Anomalie und ihre Vererbung bei Mensch und Tier. Erbarzt 10, 175–188 (1942).
Naitana, S.: Le alterazioni scheletriche nel morbo di Cooley. Arch. Pat. Clin. med. 30, 159–194 (1952).
Neel, J. V., H. A. Itano and J. S. Lawrence: Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin. Blood 8, 434–443 (1953).
Nieddu, G., e B. Ventura: Aspetti odontostomatologici del morbo di Cooley. Minerva stomat. 2, 182–188 (1953).
Noordenbos, W.: Occurrence of congenital hemolytic jaundice combined with mongolism, towershaped skull and other skeletal abnormalities in child of 6. Ned. T. Gleneesk. 1, 1012–1017 (1929).
Ortolani, M.: Über die sogenannte Cooleysche Erkrankung. Mschr. Kinderheilk. 71, 174–179 (1937).
——— Emo-osteopatia di Cooley. Minerva med. 1, 191–195 (1937).
——— La diagnosi di anemia di Cooley. Gazz. med. ital. 104, 29–65 (1946).
——— Antagonismo della talassemia maior con talune altre forme morbose. Boll. Soc. ital. emat. 2, 169–170 (1954).
———, e G. Castagnari: Contributo casistico allo studio della emoosteopatia di Cooley. Lattante 7, 777–799 (1936).
Pachioli, R.: La mielosi eritremica cronica tipo Cooley. Clin. pediat. (Bologna) 22, 233–286 (1940).
Papastavros, C. S.: Aseptic necrosis of the femoral head due to sickle cell thalassemia disease. Delaware med. J. 29, 94–96 (1957).
Paradiso, F.: Su alcuni casi di anemia con eritroblastosi ed alterazioni scheletriche a base prevalentemente osteoporotica. Pediat. med. prat. 9, 519–551 (1934).
Patrassi, G., e V. Taglioni: L’ittero emolitico costituzionale elittopoichilocitico. Padova: Cedam 1946.
Pelger, K.: Demonstratie van een paar zeldzaam voorkomende typen van bloedlichaampjes enbespreking der patienten. Ned. T. Geneesk. 72, 1178 (1928).
Perosa, L., e F. Viterbo: Studio radiologico sulle lesioni ossee nell’ittero emolitico con iperresistenza globulare. Boll. Soc. ital. Biol. sper. 22, 1063–1064 (1946).
———, e F. Viterbo : Contributo allo studio radiologico e patogenetico delle alterazioni scheletriche negli itteri con iperresistenza globulare. Arch. E. Maragliano Pat. Clin. 3, 403–432 (1948).
Piguet, B., et J. Ecoiffier: Maladie hémolitique (type Minkowski-Chauffard) et malformations veineuses congenitales. Presse méd. 67, 381–382 (1959).
Pincherle, M., e O. Scaglietti: Mielosi eritremica osteopatica (sindrome tipo Cooley). Arch. ital. Pediat. 6, 101–175 (1938).
Pizon, P.: Manifestations osseuses de la maladie de Cooley. Presse méd. 61, 418–419 (1953).
Polosa, P., e L. Ferreri: Il morbo di Cooley nell’adulto. Haematologica 41, 81–115 (1956).
Pontoni, L.: Emopatie familiari. Relaz. 50. Congr. Soc. It. Med. Int. Roma, Pozzi 1949.
Powell, M. N., J. G. Rodarte and J. V. Neel: The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia. Blood 5, 886–897 (1950).
Prowler, J. R., and E. W. Smith: Dental bone changes occurring in sickle cell disease and abnormal hemoglobin traits. Radiology 65, 762–769 (1955).
Puntoni, V.: La microcitemia ed il morbo di Cooley. Gazz. Sanitaria 30, 411–414 (1959).
Rarer, A. B.: Sickle cell disease in Africa and America; comparison. J. trop. Med. Hyg. 53, 49–53 (1950).
Reich, R. S., and N. J. Rosenberg: Aseptic necrosis of bone in Caucasians with chronic hemolytic anemia due to combined sickling and thalassemia traits. J. Bone Jt Surg. A 35, 894–904 (1953).
Reilly, W. A.: Granules in the leukocytes in Gargoylism. Amer. J. Dis. Child. 62, 489–491 (1941).
———, and S. Lindsay: Gargoylism (lipochondrodystrophy) review of clinical observations in 18 cases. Amer. J. Dis. Child. 75, 595–607 (1948).
Rietti, F.: Hemolytic anemias with increased osmotic resistence of the erythrocytes. Acta med. scand. 125, 451–464 (1946).
Robecchi, A., e F. P. Sacca’: Sopra un caso di ittero emolitico costituzionale con cirrosi epatica, ipogenitalismo ed alterazioni scheletriche. Haematologica 26, 325–371 (1944).
Robinson, I. B., and B. G. Sarnat: Roentgen studies of the maxillae and mandible in sickle cell anemia. Radiology 58, 517–523 (1952).
Romeo, F.: Anemia microdrepanocitica (studio clinico ed emato-istologico). Haematologica 39, 1–36 (1955).
Rosenow, C.: Quoted by Bernard et Coll.
Rowe, C. W., and M. E. Haggard: Bone infarcts in sickle cell anemia. Radiology 68, 661–668 (1957).
Salomoni, I.: Le alterazioni scheletriche nel morbo di Cooley. Nunt. radiol. (Roma) 21, 725–787 (1955).
Sansone, G., e S. Mastragostino : Le alterazioni dello scheletro nelle emopatie. Minerva pediat. 7, 1569–1608 (1955).
———, e F. P. Zappa: Le alterazioni dello scheletro nell’ittero emolitico costituzionale tipo Minkowski-Chauffard. Minerva pediat. 7, 1714–1718 (1955).
Scott, R. B., T. W. Davis, A. D. Ferguson and H. T. Corrington: Sickle cell anemia in children; x-ray findings. Postgrad. med. J. 22, 622–631 (1957).
Scuro, L. A., M. Muzzolini e F. Pericoli-Ridolfini: Osservazioni cliniche ed ematologiche su due casi di anemia microdrepanocitica. Atti VII. Congr. Int. Soc. Hemat. 2, 471–477 (1959).
Silvestroni, E.: Moderni orientamenti sui fattori etiopatogenetici del morbo di Cooley. Policlinico, Sez. prat. 54, 1147–1152 (1947).
——— Microcitemia costituzionale e malattie a substrato microcitemico costituzionale. Emopatie familiari. Relaz. 50. Congr. Soc. It. Med. Int., pp. 108–235, Roma 1949.
———, e I. Bianco: Una nuova entità nosologica: “la malattia micro-drepanocitica”. Haematologica 29, 455–488 (1946).
——— ——— Una particolare anomalia ematologica: la “microcitemia”. Minerva med. 2, 206–211 (1946).
——— ——— Singolare associazione di anemia microcitica costituzionale con drepanocito-anemia in soggetto di razza bianca. Policlinico, Sez. prat. 53, 265–287 (1946c).
——— ——— Alcuni dati riassuntivi di ricerche cliniche, genetiche ed ematologiche sui rapporti fra anemia microcitica costituzionale e morbo di Cooley. Minerva med. 1, 587–588 (1947).
——— ——— Un nuovo caso di malattia microdrepanocitica. Policlinico, Sez. prat. 55, 1207–1212 (1948).
——— ——— Ricerche cliniche, genetiche ed ematologiche sui malati di anemia microcitica costituzionale e di morbo di Cooley. Haematologica 31, 135–190 (1948).
——— ——— Contributo alla conoscenza dell’ellipsocitemia pura costituzionale e dell’anemia ellipsocitica. Policlinico, Sez. prat. 55, 844–848 (1948).
——— ——— Ricerche sull’anemia drepanocitica e microdrepanocitica in Sicilia e in Calabria. Policlinico, Sez. prat. 56, 501–508 (1949).
——— ——— La malattia microdrepanocitica. Pediatria (Napoli) 61, 11–26 (1953).
——— ——— La malattia microdrepanocitica. Roma: II pensiero scientifico 1955.
——— ——— M. Muzzolini e L. Roberti: U quadro emoglobinico nella malattia microdrepanocitica e nell’anemia drepanocitica. Progr. med. 16, 37–44 (I960).
Simonetti, C.: Studio radiologico delle lesioni ossee nel morbo di Cooley. Clinica (Bologna) 6, 9–41 (1940).
Smith, C. H.: Detection of mild types of mediterranean (Cooley’s) anemia. Amer. J. Dis. Child. 75, 505–527 (1948).
Smith, E. W., and C. L. Conley: Clinical features of genetic variants of sickle cell disease. Bull. Johns Hopk. Hosp. 94, 289–318 (1954).
Smith, W. S. : Sickle cell anemia and salmonella osteomyelitis. Ohio St. med. J. 49, 692–695 (1953).
Sulis, E., e G. P. Carta: Peculiarità radiomorfologiche dell’osteopatia di Cooley nel-l’adulto. Radiologia (Roma) 15, 563–574 (1959).
Tanaka, K. R., G. O. Clifford and A. R. Axelrod : Sickle cell anemia (homozygous S) with aseptic necrosis of femoral head. Blood 11, 998–1008 (1956).
Tori, G.: Clinical and radiological observations on 102 cases of sickle cell anemia. Radiol. Clin. (Basel) 23, 87–108 (1954).
——— Alterazioni ossee nell’anemia drepanocitica. Minerva pediat. 7, 585–591 (1955).
Toti, A.: Contributo allo studio delle alterazioni ossee nell’emoosteopatia di Cooley. Tesi perfezionamento Radiologia Univ. Padova 1945.
——— Le fratture traumatiche nel morbo di Cooley. Ann. Radiol. diagn. (Bologna) 23, 81–92 (1951)
Undritz, E.: Über das Vorkommen einer Familie im Wallis mit „pseudoregenerativem“ weißem Blutbild (Pelgersche Varietät). Folgerungen für die Haematologie. Schweiz. med. Wschr. 64, 10–12 (1934).
——— Blut und Knochenmarkuntersuchungen; 1. Neue Ergebnisse von Blut- und Knochenmarkuntersuchungen bei Vollträgern und dem Teilträger der Peiger-Huëtschen Varietät. Dtsch. med. Wschr. 63, 1686–1690 (1937).
——— Das Peiger-Huëtsche Blutbild beim Tier und seine Bedeutung für die Entwicklungsgeschichte des Blutes. Schweiz. med. Wschr. 69, 1177–1186 (1939).
Valentino, L.: La drepanocitosix con particolare riguardo alle osservazioni italiane. Pediatria (Napoli) 62, 257–281 (1954).
Victor, A. B., and L. E. Imperiale: The pulmonary and small bone changes in infants with sickle cell anemia. N. Y. St. J. Med. 57, 1403–1408 (1957).
Vigliani, F.: Considerazioni sull’aspetto radiologico dello scheletro in 16 casi di anemia mediterranea tipo Cooley. Minerva pediat. 7, 1665–1768 (1955).
Wade, L. J., and L. D. Stevenson: Necrosis of the bone marrow with fat embolism in sickle cell anemia. Amer. J. Path. 17, 47–54 (1941).
Wakefield, E. G., S. C. Dellinger and J. D. Camp: A study of the osseous remains of the “Mount Builders” of eastern Arkansas. Amer. J. med. Sci. 193, 488–495 (1937).
Whipple, G. H., and W. L. Bradford: Racial or familial anemia of children associated with fundamental disturbances of bone and pigment metabolism. Amer. J. Dis. Child. 44, 336–365 (1932).
Wigh, R., and H. J. Thompson jr.: Cortical fissuring in osteomyelitis complicating sickle cell anemia. Radiology 55, 553–556 (1950).
Williams, H. U.: Human paleopathology, with some original observations on simmetrical osteoporosis of skull. Arch. Path. 7, 839–902 (1929).
Wintrobe, M. M.: Sickle cell anemia. New York: Oxford University Press 1950.
Zunin, G., e E. de Toni: Comportamento dell’età scheletrica nella malattia di Cooley e nell’ittero emolitico costituzionale. Minerva pediat. 7, 17I8–1722 (1955).
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Tori, G. (1968). Osseous alterations appearing in association with haemopathies of constitutional nature. In: Diethelm, L. (eds) Röntgendiagnostik der Skeleterkrankungen Teil 3 / Diseases of the Skeletal System (Roentgen Diagnosis) Part 3. Handbuch der Medizinischen Radiologie / Encyclopedia of Medical Radiology, vol 5 / 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-95046-9_13
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