Ribbans W J
Northwick Park Hospital, Harrow.
J Hand Surg Br. 1988 Nov;13(4):463-5. doi: 10.1016/0266-7681_88_90181-7.
Two unusual cases of Kienböck's disease are reported. The first is of a young woman whose presenting feature was spontaneous rupture of the flexor pollicis longus tendon. This is the first reported case in which such a rupture was the presenting feature of the condition. The second is of a 71-year-old woman with scleroderma and Raynaud's disease who did not develop her Kienböck's disease until late in life. The literature contains no older patient with this condition and a likely association is made between the avascular necrosis and the vasculitis associated with this connective tissue disorder.
报告了两例罕见的月骨无菌性坏死病例。第一例是一名年轻女性,其主要症状是拇长屈肌腱自发性断裂。这是首例报道的以这种断裂为该病症主要症状的病例。第二例是一名患有硬皮病和雷诺氏病的71岁女性,她直到晚年才患上月骨无菌性坏死。文献中没有该病症的老年患者,并且可能在缺血性坏死与这种结缔组织疾病相关的血管炎之间存在关联。