FIBROUS DYSPLASIA OF BONE - REVIEW OF 24 CASES

被引:82
作者
FIRAT, D
STUTZMAN, L
机构
关键词
D O I
10.1016/0002-9343(68)90112-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Twenty-four cases of fibrous dysplasia were studied and clinical features reviewed. Three cases of particular interest are presented in detail. In one, both pituitary gigantism (in addition to severe deformity of facial bones) and hyperthyroidism were present. In the other two, familial hyperparathyroidism and fibrous dysplasia were present, a combination not previously reported. These latter two cases suggest the possibility that hyperparathyroidism may be another endocrinopathy associated with fibrous dysplasia and that this syndrome may also be familial. © 1968.
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页码:421 / &
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共 17 条
[1]   Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females - Report of five cases [J].
Albright, F ;
Butler, AM ;
Hampton, AO ;
Smith, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1937, 216 :727-746
[2]  
BERNIER JL, 1960, ATLAS TUMOR PATHOLOG, P61
[3]  
CAFFEY J, 1951, PEDIATRIC XRAY DIAGN, P814
[4]  
COLEY BL, 1960, NEOPLASMS BONE RELAT, P16
[5]   ADRENAL MEDULLARY + THYROID RELATIONSHIPS [J].
HARRISON, TS .
PHYSIOLOGICAL REVIEWS, 1964, 44 (02) :161-+
[6]   Hyperparathyroidism: Generalized osteitis fibrosa. With observations upon the bones, the parathyroid tumours, and normal parathyroid glands. [J].
Hunter, D ;
Turnbull, HM .
BRITISH JOURNAL OF SURGERY, 1931, 19 (74) :203-284
[7]  
Jaffe, 1958, TUMORS TUMOROUS COND, P298
[8]  
JAFFE HL, 1946, NEW YORK ACAD MED, V22, P586
[9]  
JAFFE HL, 1958, TUMORS TUMOROUS COND, P116
[10]  
Lichtenstein L, 1942, ARCH PATHOL, V33, P777