Suppr超能文献

Sweet综合征作为一名婴儿慢性肉芽肿病的首发表现。

Sweet syndrome as the presenting manifestation of chronic granulomatous disease in an infant.

作者信息

Sedel D, Huguet P, Lebbe C, Donadieu J, Odièvre M, Labrune P

机构信息

Service de Pédiatrie, Hôpital Antoine Béclère, Clamart, France.

出版信息

Pediatr Dermatol. 1994 Sep;11(3):237-40. doi: 10.1111/j.1525-1470.1994.tb00593.x.

Abstract

A 2.5-month-old infant had Sweet syndrome. Chronic granulomatous disease was subsequently diagnosed by the nitroblue tetrazolium reduction test. To date, this infant is the youngest reported with Sweet syndrome. Moreover, the association of chronic granulomatous disease with this syndrome has not been previously described. The precise relationship between the conditions remains to be determined. Granulocyte function should be evaluated in any infant with Sweet syndrome.

摘要

一名2.5个月大的婴儿患有Sweet综合征。随后通过硝基蓝四唑还原试验诊断出慢性肉芽肿病。迄今为止,该婴儿是报道中患有Sweet综合征最年幼的病例。此外,慢性肉芽肿病与该综合征的关联此前尚未有过描述。这两种病症之间的确切关系仍有待确定。对于任何患有Sweet综合征的婴儿,都应评估粒细胞功能。

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