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日本嗜酸性筋膜炎患者的特征:一项简要的多中心研究。

Characteristics of Japanese patients with eosinophilic fasciitis: A brief multicenter study.

机构信息

Department of Dermatology, Fukushima Medical University, Fukushima, Japan.

Department of Dermatology, University of Tokyo, Tokyo, Japan.

出版信息

J Dermatol. 2020 Dec;47(12):1391-1394. doi: 10.1111/1346-8138.15561. Epub 2020 Aug 29.

Abstract

Eosinophilic fasciitis is a relatively rare cutaneous fibrotic condition affecting the deep fascia of the extremities, with or without peripheral blood eosinophilia. To examine the characteristics of Japanese patients with eosinophilic fasciitis, we conducted a brief, multicenter, retrospective survey at seven university hospitals. In total, 31 patients were identified as having eosinophilic fasciitis, among whom 30 patients fulfilled the Japanese diagnostic criteria. The male : female ratio was 2.3:1, and the mean age was 47.7 years. Three of the patients were under 20 years old. The possible triggering factors included muscle training, sports, walking or sitting for a long time, physical work, insect bite and drug. Co-occurrence of morphea was observed in nine cases (29%), and malignancies were associated in three (two hematological malignancies and one internal malignancy). Immunological abnormalities in the serum showed positive antinuclear antibody, positive rheumatoid factor, increased aldolase levels and increased immunoglobulin G levels. The patients were treated with either monotherapy or combination therapy by oral prednisolone (20-80 mg/day), methotrexate (6-10 mg/week), cyclosporin (100-150 mg/day), mizoribine, infliximab and phototherapy. Methylprednisolone pulse therapy was performed in six cases. By contrast, spontaneous improvement due to resting only was observed in two cases, and skin hardening was improved by withdrawal of the anticancer drug in one case. This study suggests several characteristics of Japanese patients with eosinophilic fasciitis, namely male predominance, rare pediatric occurrence, immunological abnormalities and coexistence with morphea. Systemic prednisolone is the first-line therapy, but pulse therapy is occasionally required for severe cases. The triggering events of physical stress are not so frequent as have previously been reported, and various factors or even unknown factors may be associated with the induction of eosinophilic fasciitis.

摘要

嗜酸性筋膜炎是一种相对罕见的皮肤纤维性疾病,影响四肢的深部筋膜,伴有或不伴有外周血嗜酸性粒细胞增多。为了研究日本嗜酸性筋膜炎患者的特征,我们在七所大学医院进行了一项简短的、多中心的回顾性调查。共确定 31 例嗜酸性筋膜炎患者,其中 30 例符合日本诊断标准。男女比例为 2.3:1,平均年龄为 47.7 岁。有 3 例患者年龄小于 20 岁。可能的诱发因素包括肌肉训练、运动、长时间行走或坐着、体力劳动、昆虫叮咬和药物。9 例(29%)合并硬斑病,3 例(2 例血液系统恶性肿瘤和 1 例内脏恶性肿瘤)合并恶性肿瘤。血清免疫学异常表现为抗核抗体阳性、类风湿因子阳性、醛缩酶水平升高和免疫球蛋白 G 水平升高。患者接受泼尼松龙(20-80mg/d)、甲氨蝶呤(6-10mg/周)、环孢素(100-150mg/d)、吗替麦考酚酯、英夫利昔单抗和光疗的单一或联合治疗。6 例患者接受了甲泼尼龙冲击治疗。相反,仅休息即可自发改善的有 2 例,因停用抗癌药物皮肤硬化改善的有 1 例。本研究提示日本嗜酸性筋膜炎患者具有以下特征:男性多见、儿童发病罕见、免疫异常和与硬斑病并存。全身泼尼松龙是一线治疗,但严重病例偶尔需要脉冲治疗。物理应激的诱发事件并不像以前报道的那样频繁,各种因素甚至未知因素可能与嗜酸性筋膜炎的发生有关。

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