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一例罕见的进行性系统性硬化症病例,发病于儿童早期,继发于传染性单核细胞增多症。

Unusual case of progressive systemic sclerosis with onset in early childhood and following infectious mononucleosis.

作者信息

Urano J, Kohno H, Watanabe T

出版信息

Eur J Pediatr. 1981 Jul;136(3):285-9. doi: 10.1007/BF00442996.

Abstract

A rare case of infantile progressive systemic sclerosis is reported. A Japanese girl suffered from infectious mononucleosis at the age of 1 year 3 months, and 5 months later she developed edema and sclerosis of the skin. She has been followed up for 4 years and now has grotesque features, with contractures of hands and feet due to advanced systemic sclerosis. The relationship between infectious mononucleosis and progressive systemic sclerosis is discussed.

摘要

报告了一例罕见的婴儿进行性系统性硬化症病例。一名日本女孩在1岁3个月时患传染性单核细胞增多症,5个月后出现皮肤水肿和硬化。她已接受随访4年,目前因晚期系统性硬化症而出现面容怪异,伴有手足挛缩。文中讨论了传染性单核细胞增多症与进行性系统性硬化症之间的关系。

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