Suppr超能文献

成年晚期以难治性肺炎为表现的慢性肉芽肿病。

Chronic granulomatous disease presenting as refractory pneumonia in late adulthood.

作者信息

Sarwar Ghulam, de Malmanche Theo, Rassam Loui, Grainge Christopher, Williams Andrew, Arnold David

机构信息

Department of Medicine, John Hunter Hospital New Lambton, New South Wales, Australia ; School of Medicine and Public Health, The University of Newcastle Newcastle, New South Wales, Australia.

School of Medicine and Public Health, The University of Newcastle Newcastle, New South Wales, Australia ; Immunology, Hunter Area Pathology Service New Lambton, New South Wales, Australia.

出版信息

Respirol Case Rep. 2015 Jun;3(2):54-6. doi: 10.1002/rcr2.99. Epub 2015 Mar 24.

Abstract

We present a case of refractory pneumonia in an adult patient with underlying chronic granulomatous disease (CGD). Her lobectomy tissue grew B urkholderia cepacia and histopathology revealed diffuse severe pneumonic consolidation with suppurative/necrotizing granulomata. An initial attempt to find an underlying immune deficiency was unsuccessful. Following recurrent invasive infections, repeat immunological assessment revealed reduced neutrophil function, demonstrating skewed carrier status (lyonization) for X-linked CGD (only 3% normal cells). A pathogenic mutation in the CYBB gene was found on sequencing. CYBB gene encodes the gp91phox, a catalytic subunit of nicotinamide adenine dinucleotide phosphate-oxidase that produces reactive oxygen species in phagocytes. Lyonization increases with age, explaining the delayed clinical CGD. CGD is a rare neutrophil disorder that usually presents in early life with recurrent infections due to bacteria and fungi primarily involving lungs and skin. It is secondary to a defective NADPH oxidase system needed to kill intracellular organisms and activate the formation of neutrophil extracellular traps.

摘要

我们报告一例患有潜在慢性肉芽肿病(CGD)的成年患者的难治性肺炎病例。她的肺叶切除组织培养出洋葱伯克霍尔德菌,组织病理学显示弥漫性严重肺实变伴化脓性/坏死性肉芽肿。最初寻找潜在免疫缺陷的尝试未成功。在反复发生侵袭性感染后,重复免疫评估显示中性粒细胞功能降低,表明X连锁CGD存在偏态携带者状态(莱昂化,即失活X染色体随机化,仅3%正常细胞)。测序发现CYBB基因存在致病突变。CYBB基因编码gp91phox,它是烟酰胺腺嘌呤二核苷酸磷酸氧化酶的催化亚基,在吞噬细胞中产生活性氧。莱昂化随年龄增加,这解释了CGD的临床症状延迟出现。CGD是一种罕见的中性粒细胞疾病,通常在生命早期出现,主要由细菌和真菌引起反复感染,主要累及肺部和皮肤。它继发于杀死细胞内病原体和激活中性粒细胞胞外陷阱形成所需的NADPH氧化酶系统缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d75/4469140/f40a435734a6/rcr20003-0054-f1.jpg

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