Erasmus Syndrome: Co-existence of silicosis and progressive systemic sclerosis in a 55 year old male

Jitendra Jalutharia, R. Dixit
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引用次数: 1

Abstract

The Erasmus syndrome describes the association of generalised progressive scleroderma following exposure to silica with or without silicosis. We report a case of Erasmus Syndrome in a 55-year old labourer presenting with shortness of breath, arthralgia, Raynaud’s phenomenon, skin tightening and microstomia along with pulmonary arterial hypertension. Among investigations, serological markers were strongly positive, high-resolution computed tomography chest showed evidence of interstitial lung disease (ILD) with mediastinal lymphadenopathy and histopathology of skin biopsy were suggestive of systemic sclerosis. Correlating the occupational history, clinical features, haematological investigations and histological findings, a diagnosis of Erasmus syndrome was safely made.
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伊拉斯谟综合征:55岁男性并发矽肺和进行性系统性硬化
伊拉斯谟综合征描述了暴露于二氧化硅后伴有或不伴有矽肺的全身性进行性硬皮病的关联。我们报告一位55岁劳工的伊拉斯谟症候群,表现为呼吸短促、关节痛、雷诺氏现象、皮肤紧绷及小口畸形并肺动脉高压。在调查中,血清学指标呈强烈阳性,高分辨率胸部计算机断层扫描显示间质性肺疾病(ILD)伴纵隔淋巴结病,皮肤活检组织病理学提示系统性硬化症。结合职业史、临床特征、血液学调查和组织学发现,诊断为伊拉斯谟综合征是安全的。
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审稿时长
20 weeks
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