Joseph B, Chacko V
Radiology. 1985 Feb;154(2):343-4. doi: 10.1148/radiology.154.2.3966121.
The authors report two cases of marked acro-osteolysis. One patient, a 16-year-old boy, had hypertrophic pulmonary osteoarthropathy associated with bronchiectasis, clubbing of the digits, synovitis, and osseous changes. The other patient, a 55-year-old man, had pachydermoperiostosis as well as synovial hypertrophy, clubbing of the digits, blepharitis, and a cataract. While the association of acro-osteolysis and pachydermoperiostosis has been reported before, this appears to be the first verified case of acro-osteolysis combined with hypertrophic pulmonary osteoarthropathy.
作者报告了两例明显的肢端骨质溶解病例。一名患者为16岁男孩，患有与支气管扩张相关的肥厚性肺骨关节病，伴有手指杵状指、滑膜炎和骨质改变。另一名患者为55岁男性，患有厚皮性骨膜病以及滑膜肥厚、手指杵状指、睑缘炎和白内障。虽然之前已有肢端骨质溶解与厚皮性骨膜病相关联的报道，但这似乎是第一例经证实的肢端骨质溶解合并肥厚性肺骨关节病的病例。
