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嗜酸性筋膜炎——进展为线状硬皮病:一例报告

Eosinophilic fasciitis--progression to linear scleroderma: a case report.

作者信息

Balat A, Akinci A, Turgut M, Mizrak B, Aydin A

机构信息

Department of Pediatrics, Inönü University Faculty of Medicine, Malatya.

出版信息

Turk J Pediatr. 1999 Jul-Sep;41(3):381-5.

Abstract

Eosinophilic fasciitis is a rare disease in children. Although changes similar to linear scleroderma have been reported, the outcome is usually good. In this report, a 10-year-old boy who developed eosinophilic fasciitis without a good response to steroids is presented. He progressed to linear scleroderma within months. Our case reinforces the hypothesis that eosinophilic fasciitis may be an early manifestation or a variant of localized scleroderma similar to the other cases in the literature.

摘要

嗜酸性筋膜炎在儿童中是一种罕见疾病。尽管已有类似线状硬皮病改变的报道,但预后通常良好。在本报告中,介绍了一名10岁男孩,他患嗜酸性筋膜炎,对类固醇治疗反应不佳。他在数月内进展为线状硬皮病。我们的病例强化了这样一种假说,即嗜酸性筋膜炎可能是局限性硬皮病的早期表现或一种变体,类似于文献中的其他病例。

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