Clinical manifestations of 42 Moroccan patients with chronic granulomatous disease.

Q3 Medicine
Qatar Medical Journal Pub Date : 2025-03-21 eCollection Date: 2025-01-01 DOI:10.5339/qmj.2025.14
Assma Dably, Ibtihal Benhssaein, Jalila El Bakkouri, Asmaa Drissi Bourhanbour, Leila Jeddane, Ahmed Aziz Bousfiha, Fatima Ailal
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引用次数: 0

Abstract

Background: Chronic granulomatous disease (CGD) is a primary immunodeficiency due to alterations in the oxidative metabolism of phagocytic cells. This condition is characterized by serious and recurrent infections caused by pyogenic bacteria, particularly Staphylococcus aureus, and fungal pathogens such as Aspergillus. These infections are associated with granuloma formation and inflammatory manifestations.The aim of our study was to report the clinical characteristics, microbiological aspects and outcomes, and prognosis of a cohort comprising 42 Moroccan patients suffering from CGD.

Methods: A total of 42 patients were diagnosed for family history, consanguinity, and both clinical and laboratory findings.The diagnosis was confirmed by assessing neutrophil oxidative burst activity, using either the nitroblue tetrazolium (NBT) test or the dihydrorhodamine (DHR) test.

Results: The cohort comprised children from 34 different families, including 12 siblings. The age of onset ranged from 4 days to 13 years, with the diagnosis being established between the ages of 25 days and 13 years. The predominant clinical manifestations were skin infections, lymphadenopathy, pneumonia, BCGitis, liver abscess, pulmonary aspergillosis, and inflammatory colitis. The most frequently isolated germs were Aspergillus, Serratia, and Staphylococcus. Among the total of 42 patients, 17 fatalities occurred, with aspergillosis being identified as the primary cause of their deaths.

Conclusions: In this study, the clinical characteristics and isolated microorganisms correspond to the pathogens known to be important in CGD. Lung infections represent the most prevalent complication and significantly contribute to high mortality rates, particularly in the case of Aspergillus pneumonia, which is known for its tendency to disseminate. Additionally, BCGitis has been frequently observed in countries where the BCG (Bacille Calmette-Guérin) vaccination is routinely administered. Enterocolitis emerges as the most common inflammatory complication in clinical settings. Unfortunately, CGD remains largely unknown in Morocco, highlighting the urgent need to raise awareness among doctors. This increased awareness could facilitate early diagnosis and improve patient prognosis.

42例摩洛哥慢性肉芽肿病的临床表现
背景:慢性肉芽肿病(CGD)是一种由吞噬细胞氧化代谢改变引起的原发性免疫缺陷。这种疾病的特点是由化脓性细菌,特别是金黄色葡萄球菌和真菌病原体如曲霉引起的严重和反复感染。这些感染与肉芽肿形成和炎症表现有关。本研究的目的是报道42名摩洛哥CGD患者的临床特征、微生物学方面和预后。方法:对42例患者进行家族史、血亲史、临床及实验室检查。通过硝基蓝四氮唑(NBT)试验或二氢霍达明(DHR)试验评估中性粒细胞氧化爆发活性来确诊。结果:该队列包括来自34个不同家庭的儿童,包括12个兄弟姐妹。发病年龄从4天到13岁不等,诊断年龄在25天到13岁之间。主要临床表现为皮肤感染、淋巴结病、肺炎、BCGitis、肝脓肿、肺曲霉病、炎性结肠炎。最常见的分离细菌是曲霉、沙雷氏菌和葡萄球菌。在总共42名患者中,有17人死亡,曲霉病被确定为其死亡的主要原因。结论:在本研究中,临床特征和分离的微生物与已知的CGD重要病原体相对应。肺部感染是最普遍的并发症,并显著导致高死亡率,特别是曲霉性肺炎,众所周知,它具有传播的倾向。此外,在常规接种卡介苗(Bacille calmette - gusamrin)疫苗的国家经常观察到BCGitis。小肠结肠炎是临床上最常见的炎症并发症。不幸的是,CGD在摩洛哥基本上仍然不为人所知,这突出表明迫切需要提高医生的认识。这种意识的提高可以促进早期诊断和改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Qatar Medical Journal
Qatar Medical Journal Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
77
审稿时长
6 weeks
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