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舒尔曼综合征:嗜酸性筋膜炎(作者译)

[Shulman's syndrome: eosinophilic fasciitis (author's transl)].

作者信息

Thivolet J, Jeune R, Faure M, Hermier C, Michel F

出版信息

Ann Dermatol Venereol. 1979 Nov;106(11):859-66.

PMID:539697
Abstract

A detailed report is made of the clinical, histological, biological manifestations of eosinophilic fasciitis, i. e. the Shulman's syndrome, about a 53-year-old man. An extreme induration of sub-cutaneous tissues from arms, legs and trunk, without involvement of the face and extremities, was associated with severe thickening of deep peri-muscular fascias. Raynaud's phenomenon was absent, as were morpheas and visceral involvement. Results of biopsies studied by standard, electron and I. F. microscopy, revealed sclerosis and cellular infiltrates (lymphocytes, plasma cells, histiocytes and eosinophils) in fascia and muscular septa; no changes were seen in epidermis, dermis or sub-cutaneous fat tissue. An elevated ESR, eosinophilia and hyperimmunoglobulinaemia with high levels of circulating immune complexes were the only biological abnormalities. A good response to systemic corticosteroid therapy was observed. These features were similar to those seen in other cases of eosinophilic fasciitis. The etiology and pathogenesis of the Shulman's syndrome remain unclear. A critical review of the literature suggests that eosinophilic fasciitis should be separated from scleroderma and pseudoscleroderma, although this opinion has been discussed.

摘要

本文详细报告了一名53岁男性嗜酸性筋膜炎(即舒尔曼综合征)的临床、组织学和生物学表现。患者手臂、腿部和躯干的皮下组织出现极度硬结,但面部和四肢未受累,同时伴有深部肌周筋膜的严重增厚。患者无雷诺现象,也无硬斑病和内脏受累情况。通过标准显微镜、电子显微镜和免疫荧光显微镜检查活检结果,发现筋膜和肌间隔有硬化及细胞浸润(淋巴细胞、浆细胞、组织细胞和嗜酸性粒细胞);表皮、真皮或皮下脂肪组织未见变化。唯一的生物学异常是血沉升高、嗜酸性粒细胞增多和高免疫球蛋白血症以及循环免疫复合物水平升高。观察到患者对全身皮质类固醇治疗反应良好。这些特征与其他嗜酸性筋膜炎病例所见相似。舒尔曼综合征的病因和发病机制仍不清楚。对文献的批判性回顾表明,尽管这一观点存在争议,但嗜酸性筋膜炎应与硬皮病和假性硬皮病区分开来。

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