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52岁时出现暴发性堆肥肺炎的慢性肉芽肿病。

Chronic granulomatous disease presenting at age 52 with fulminant mulch pneumonitis.

作者信息

Marois Louis, Drouin David, Leduc Charles, Fernandez Isabel, Manganas Hélène, Gosse Géraldine, Chapdelaine Hugo, Cros Guilhem, Falcone Emilia Liana

机构信息

Department of Medicine, Université de Montreal, Montreal, Québec, Canada.

Institut de recherches cliniques de Montréal, Montreal, Québec, Canada.

出版信息

J Allergy Clin Immunol Glob. 2022 Sep 2;1(4):322-324. doi: 10.1016/j.jacig.2022.06.004. eCollection 2022 Nov.

DOI:10.1016/j.jacig.2022.06.004
PMID:37779538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10509940/
Abstract

Chronic granulomatous disease should be considered in adults of any age in the presence of refractory and/or atypical or fulminant pulmonary infections. This case of new large deletions in was presented with mulch pneumonitis without a significant history of infections.

摘要

在存在难治性和/或非典型或暴发性肺部感染的情况下,任何年龄的成年人都应考虑慢性肉芽肿病。该例出现新的大片段缺失并伴有腐殖质肺炎,既往无明显感染史。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64af/10509940/8bc4cc391972/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64af/10509940/eb051c378d9b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64af/10509940/8bc4cc391972/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64af/10509940/eb051c378d9b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64af/10509940/8bc4cc391972/gr2.jpg

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本文引用的文献

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Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults.慢性肉芽肿病的造血细胞移植:712例儿童和成人的研究
Blood. 2020 Sep 3;136(10):1201-1211. doi: 10.1182/blood.2020005590.
2
Late diagnosis of chronic granulomatous disease.慢性肉芽肿病的迟诊。
Clin Exp Immunol. 2020 Sep;201(3):297-305. doi: 10.1111/cei.13474. Epub 2020 Jul 13.
3
Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran.导致原发性免疫缺陷疾病的基因突变:来自伊朗首个原发性免疫缺陷生物样本库的报告。
一名患有慢性肉芽肿病的患者并发肺炎、肋骨骨髓炎、脊椎椎间盘炎、椎旁及硬膜外脓肿的罕见病例。
Clin Case Rep. 2023 May 12;11(5):e7341. doi: 10.1002/ccr3.7341. eCollection 2023 May.
Allergy Asthma Clin Immunol. 2016 Dec 2;12:62. doi: 10.1186/s13223-016-0166-5. eCollection 2016.
4
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.原发性免疫缺陷病:基因组学方法描绘出异质性孟德尔疾病。
J Allergy Clin Immunol. 2017 Jan;139(1):232-245. doi: 10.1016/j.jaci.2016.05.042. Epub 2016 Jul 16.
5
Pulmonary manifestations in adult patients with chronic granulomatous disease.成人慢性肉芽肿病患者的肺部表现。
Eur Respir J. 2015 Jun;45(6):1613-23. doi: 10.1183/09031936.00118414. Epub 2015 Jan 22.
6
IL-1 receptor blockade restores autophagy and reduces inflammation in chronic granulomatous disease in mice and in humans.白细胞介素-1 受体阻断可恢复慢性肉芽肿病小鼠和人类的自噬并减轻炎症。
Proc Natl Acad Sci U S A. 2014 Mar 4;111(9):3526-31. doi: 10.1073/pnas.1322831111. Epub 2014 Feb 18.
7
Newly diagnosed chronic granulomatous disease in a 44 year old male presenting with recurrent groin cellulitis and colitis.一名44岁男性新诊断出患有慢性肉芽肿病,表现为复发性腹股沟蜂窝织炎和结肠炎。
Allergy Asthma Clin Immunol. 2013 Mar 6;9(1):9. doi: 10.1186/1710-1492-9-9.
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Fulminant mulch pneumonitis: an emergency presentation of chronic granulomatous disease.暴发性覆盖物肺炎:慢性肉芽肿病的一种紧急表现。
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