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

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

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[摄入l -色氨酸引起嗜酸性粒细胞增多-肌痛综合征2例]。
嗜酸性肌痛综合征(EMS)是1989年在美国新墨西哥州报道并命名的一种新的结缔组织疾病,l -色氨酸被怀疑是EMS的病原体。这种l -色氨酸是日本制造的,但在日本没有明确的EMS病例报告。我们报告2例急诊患者。一名72岁妇女和一名74岁妇女,由同一医生同时口服l -色氨酸1 g/天,治疗4个月和5个月。两例临床病程相似。手臂出现弥漫性红斑和肿胀,并扩散到全身。皮肤病变变成了光泽性硬化症。嗜酸性粒细胞在早期是显著的。ANA、DNA抗体、ENA抗体均为阴性。神经学检查显示轻度周围神经病变。在我们的病例中,没有硬指症和雷诺现象是EMS的特征性发现。两个病例同时发病,同时使用同一种药物,暗示l -色氨酸摄入与EMS密切相关。
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