Suppr超能文献

伴有巨大淋巴结病的窦性组织细胞增多症:并发自身免疫性溶血性贫血。

Sinus histiocytosis with massive lymphadenopathy: complicated by autoimmune hemolytic anemia.

作者信息

Kiran Penukonda Sasi, Sowdi Vasantha Prema, Shetty Sumanth B, Venugopal U, Parameshwariah S, Dias Edwin, Kamala C S

机构信息

Department of Pediatrics, K.S. Hegde Medical Academy, Deralakatte, Mangalore, India.

出版信息

Indian J Pediatr. 2003 Sep;70(9):759-60. doi: 10.1007/BF02724322.

Abstract

Sinus histiocytosis with massive lymphadenopathy is a rare histiocytic disorder with very few case reports in Indian literature. Immunological abnormalities have been documented in few cases. We report one such case of a child presenting with generalized lymphadenopathy and complicated by autoimmune hemolytic anemia, suggestive of an associated immune dysfunction.

摘要

伴巨大淋巴结病的窦性组织细胞增多症是一种罕见的组织细胞疾病,印度文献中的病例报告极少。少数病例记录了免疫异常情况。我们报告了这样一例患儿,其表现为全身淋巴结病,并并发自身免疫性溶血性贫血,提示存在相关的免疫功能障碍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验