家族性肢体消失：四代特发性多中心骨质溶解症
Familial vanishing limbs: four generations of idiopathic multicentric osteolysis.
作者信息
Hemingway A P, Leung A, Lavender J P
出版信息
Clin Radiol. 1983 Sep;34(5):585-8. doi: 10.1016/s0009-9260(83)80174-3.
PMID:6617092
Abstract
A family is described which has exhibited in four generations a bizarre form of arthritis mutilans and osteolysis, the features of which seem to fit most closely with a diagnosis of hereditary multicentric osteolysis, a subgroup of idiopathic multicentric osteolysis. The differential diagnosis of arthritis mutilans associated with osteolysis is discussed; this includes a wide variety of disorders ranging from rheumatoid arthritis to rare conditions such as the Winchester syndrome.
摘要
本文描述了一个家族，该家族四代人都表现出一种怪异的残毁性关节炎和骨质溶解症，其特征似乎最符合遗传性多中心骨质溶解症的诊断，遗传性多中心骨质溶解症是特发性多中心骨质溶解症的一个亚组。文中讨论了与骨质溶解相关的残毁性关节炎的鉴别诊断；这包括从类风湿性关节炎到诸如温彻斯特综合征等罕见病症的多种疾病。
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