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首页> 外文期刊>Clinical rheumatology >Systemic sclerosis sine scleroderma presenting as pulmonary intersticial fibrosis.
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Systemic sclerosis sine scleroderma presenting as pulmonary intersticial fibrosis.

机译:系统性硬化症正弦硬皮病表现为肺间质纤维化。

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摘要

To the editor: Systemic sclerosis (SSc) is a generalized connective tissue disorder of unknown aetiology. The main types of SSc are diffuse cutaneous systemic sclerosis (dcSSc), limited cutaneous sclerosis systemic (lcSSc), systemic sclerosis sine scleroderma (ssSSc) and overlap syndromes . The ssSSc is a rare entity, scantly reported in the scientific literature , characterized by the absence of skin involvement. We present a case of a female diagnosed of ssSSc with pulmonary involvement.
机译:致编辑:系统性硬化症(SSc)是一种病因不明的广泛性结缔组织疾病。 SSc的主要类型是弥漫性皮肤系统性硬化症(dcSSc),系统性有限性皮肤硬化症(lcSSc),正弦硬皮病(ssSScc)和重叠综合征。 ssSSc是一种罕见的实体,在科学文献中很少报道,其特征是没有皮肤受累。我们介绍了一例女性被诊断为ssSSc并伴有肺部感染。

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