Chalmers I M, Bhoola K D, Parsoo I
S Afr Med J. 1979 Feb 17;55(7):262-4.
We describe a patient with a scleroderma-like illness which involved the arms and legs but not the face and hands. Clinical, laboratory and histological features were those of the recently described syndrome, eosinophilic fasciitis. This rare condition is worthy of note because it appears to have a much better prognosis than conventional scleroderma, and because it responds very well to corticosteroid therapy.
我们描述了一名患有硬皮病样疾病的患者,该疾病累及手臂和腿部,但未累及面部和手部。临床、实验室和组织学特征均符合最近描述的综合征——嗜酸性筋膜炎。这种罕见病症值得关注,因为它的预后似乎比传统硬皮病好得多,而且对皮质类固醇治疗反应良好。