Strunk R W, Scheld W M
South Med J. 1986 Nov;79(11):1425-7. doi: 10.1097/00007611-198611000-00024.
Weber-Christian disease is an uncommon disorder of unclear etiology whose unifying feature is fatty tissue inflammation. Its association with alpha 1-antitrypsin deficiency produces severe clinical manifestations. Although many agents have been used to treat Weber-Christian disease, current therapy is based on the poorly documented use of corticosteroids. We have reported the case of a young man with life-threatening Weber-Christian disease associated with alpha 1-antitrypsin deficiency unresponsive to corticosteroids who responded to cyclophosphamide.
韦格纳-克里斯蒂安病是一种病因不明的罕见疾病,其共同特征是脂肪组织炎症。它与α1-抗胰蛋白酶缺乏症相关会产生严重的临床表现。尽管已经使用了许多药物来治疗韦格纳-克里斯蒂安病,但目前的治疗方法是基于对皮质类固醇使用记录不充分的情况。我们报告了一例患有危及生命的韦格纳-克里斯蒂安病且与α1-抗胰蛋白酶缺乏症相关的年轻男子,他对皮质类固醇无反应,但对环磷酰胺有反应。