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一名患有慢性肉芽肿病儿童的卡介苗病和结核病

BCG-osis and tuberculosis in a child with chronic granulomatous disease.

作者信息

Bustamante Jacinta, Aksu Guzide, Vogt Guillaume, de Beaucoudrey Ludovic, Genel Ferah, Chapgier Ariane, Filipe-Santos Orchidée, Feinberg Jacqueline, Emile Jean-François, Kutukculer Necil, Casanova Jean-Laurent

机构信息

Laboratory of Human Genetics of Infectious Diseases, Institut National de la Santé et de la Recherche Médicale U550; University Paris René Descartes, Necker Medical School, Paris, France.

出版信息

J Allergy Clin Immunol. 2007 Jul;120(1):32-8. doi: 10.1016/j.jaci.2007.04.034. Epub 2007 Jun 4.

Abstract

A few known primary immunodeficiencies confer predisposition to clinical disease caused by weakly virulent mycobacteria, such as BCG vaccines (regional disease, known as BCG-itis, or disseminated disease, known as BCG-osis), or more virulent mycobacteria, such as Mycobacterium tuberculosis (pulmonary and disseminated tuberculosis). We investigated the clinical and genetic features of a 12-year-old boy with both recurrent BCG-osis and disseminated tuberculosis. The patient's phagocytic cells produced no O(2)(-). A hemizygous splice mutation was found in intron 5 of CYBB, leading to a diagnosis of X-linked chronic granulomatous disease. Chronic granulomatous disease should be suspected in all children with BCG-osis, even in the absence of nonmycobacterial infectious diseases, and in selected children with recurrent BCG-itis or severe tuberculosis.

摘要

一些已知的原发性免疫缺陷会使人易患由弱毒力分枝杆菌引起的临床疾病,如卡介苗(局部疾病,称为卡介苗炎,或播散性疾病,称为卡介苗病),或更强毒力的分枝杆菌,如结核分枝杆菌(肺结核和播散性结核病)。我们调查了一名患有复发性卡介苗病和播散性结核病的12岁男孩的临床和遗传特征。该患者的吞噬细胞不产生O(2)(-)。在CYBB基因的第5内含子中发现了一个半合子剪接突变,从而诊断为X连锁慢性肉芽肿病。对于所有患有卡介苗病的儿童,即使没有非分枝杆菌感染性疾病,以及对于某些患有复发性卡介苗炎或严重结核病的儿童,都应怀疑患有慢性肉芽肿病。

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