Klenk G, Rieber C, Petzel H, Lippelt C
Rofo. 1978 May;128(5):538-45. doi: 10.1055/s-0029-1230900.
Four cases of non-familiar acropathia ulcero-mutilans (Bureau-Barriere) are described. In all cases there was a history of alcoholism, abnormal liver function, painless foot ulcers and polyneuritis. The radiological changes were confined to the lower extremities. There were osteolytic changes in the metatarsal heads and the bases of the proximal phalanges, particularly of the great toes; in addition, there was general demineralisation of the bones of the feet. One case was remarkable in that the tarsal bones and the proximal protions of the metatarsals were also involved. A variety of bone deformities were observed, and there were pathological fractures as well as subluxation and dislocation. The differential diagnosis between familial and non-familial acro-osteolysis, and of some other bone abnormalities is discussed. A multifactorial pathogenesis of the disease is suggested.
本文描述了4例非典型性肢端溃疡型坏疽(Bureau-Barriere型)病例。所有病例均有酗酒史、肝功能异常、无痛性足部溃疡和多发性神经炎。放射学改变局限于下肢。跖骨头和近端趾骨基部,尤其是拇趾,出现骨质溶解改变;此外,足部骨骼普遍脱矿质。1例病例较为特殊,跗骨和跖骨近端也受累。观察到多种骨骼畸形,还出现了病理性骨折以及半脱位和脱位。文中讨论了家族性和非家族性肢端骨质溶解症以及其他一些骨骼异常的鉴别诊断。提示该病存在多因素发病机制。