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两例L-色氨酸摄入诱发的嗜酸性粒细胞增多性肌痛综合征

[Two cases of L-tryptophan ingestion induced eosinophilia-myalgia syndrome].

作者信息

Mizutani T, Mizutani H, Hashimoto K, Kishida M, Taniguchi H, Okada H, Murata M, Nakamura Y, Shimizu M

机构信息

Department of Dermatology, Mie University School of Medicine.

出版信息

Nihon Hifuka Gakkai Zasshi. 1991 Apr;101(5):561-6.

PMID:1890752
Abstract

Eosinophilia-myalgia syndrome (EMS), a new connective tissue disease was reported and named in 1989 from New Mexico, U.S.A. L-tryptophan has been suspected as the causative agent of EMS. This L-tryptophan was made in Japan, but no definite case of EMS has been reported in Japan. We report 2 patients with EMS. A 72-year-old woman and a 74-year-old woman, who had been treated with oral L-tryptophan 1 g/day for 4 and 5 months by the same doctor simultaneously. The clinical courses of the two cases were similar. A diffuse erythema and swelling appeared on the arms and spread over the whole body. The skin lesions turned into lustrous sclerosis. Eosinophilia was remarkable in the early stage. ANA, DNA anti-body and ENA antibodies were all negative. Neurological examination revealed a mild peripheral neuropathy. No sclerodactylia and no Raynaud's phenomenon in our cases are characteristic findings in EMS. The simultaneous onset of two cases using the same drug at the same time implicates the close relation of L-tryptophan ingestion to EMS.

摘要

嗜酸性粒细胞增多性肌痛综合征(EMS)是一种新的结缔组织病,1989年在美国新墨西哥州被报道并命名。L-色氨酸被怀疑是EMS的致病因素。这种L-色氨酸是日本生产的,但日本尚未报告明确的EMS病例。我们报告2例EMS患者。一名72岁女性和一名74岁女性,由同一位医生同时给予每日1克口服L-色氨酸治疗,分别持续4个月和5个月。两例的临床病程相似。双臂出现弥漫性红斑和肿胀,并蔓延至全身。皮肤病变转变为有光泽的硬化。早期嗜酸性粒细胞增多明显。抗核抗体(ANA)、DNA抗体和可提取性核抗原(ENA)抗体均为阴性。神经学检查显示轻度周围神经病变。我们的病例中无硬皮指和雷诺现象是EMS的特征性表现。两例同时使用同一药物发病提示摄入L-色氨酸与EMS密切相关。

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