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蕈样肉芽肿与职业性系统性硬化症的巧合关联?

Coincidental association of mycosis fungoides and occupational systemic sclerosis?

作者信息

Yasuda Masahito, Amano Hiroo, Yamanaka Masayoshi, Tamura Atsushi, Ishikawa Osamu

机构信息

Department of Dermatology, Gunma University Graduate School of Medicine, Gunma, Japan.

出版信息

J Dermatol. 2008 Jan;35(1):21-4. doi: 10.1111/j.1346-8138.2007.00405.x.

Abstract

We report a 58-year-old man with mycosis fungoides (MF) and occupational systemic sclerosis (SSc) induced by silica exposure. He was engaged in tunnel construction from the age of 18 to 33 years. He developed MF at the age of 30. Diagnosis of silicosis was made at the age of 52 and SSc at the age of 58. Physical examinations revealed sclerotic skin changes on his forearms and fingers and poikiloderma on the left popliteal fossa and inguinal region. Both antinuclear antibody and antitopoisomerase-I antibody were positive. We could find no apparent difference between his clinical features and those of idiopathic SSc except for the presence of silicosis and MF. Systemic therapy with interferon-gamma for MF did not improve the skin sclerosis. We discuss the relationship of silica exposure to both MF and SSc.

摘要

我们报告了一名58岁男性,患有蕈样肉芽肿(MF)以及因接触二氧化硅诱发的职业性系统性硬化症(SSc)。他从18岁至33岁从事隧道建设工作。他30岁时患上MF。52岁时诊断为矽肺,58岁时诊断为SSc。体格检查发现其前臂和手指有硬化性皮肤改变,左腘窝和腹股沟区有皮肤异色症。抗核抗体和抗拓扑异构酶-I抗体均呈阳性。除了存在矽肺和MF外,我们未发现他的临床特征与特发性SSc有明显差异。用干扰素-γ对MF进行全身治疗并未改善皮肤硬化。我们讨论了二氧化硅暴露与MF和SSc的关系。

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