[Chronic granulomatous disease as a rare differential diagnosis of inflammatory bowel disease].

IF 1.4 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Zeitschrift fur Gastroenterologie Pub Date : 2018-12-01 Epub Date: 2018-11-22 DOI:10.1055/a-0732-5865
Jan-Christopher Metzger, Elena Kurz, Caroline von Spee-Mayer, Gesa Kolck, Alexander Bogumil, Peter R Galle, Tim Zimmermann
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引用次数: 4

Abstract

Background:  Chronic granulomatous disease is a rare disease with a prevalence of approximately 150 cases in Germany. An intestinal manifestation that mimics chronic inflammatory bowel disease (IBD) has only been described in a few cases. As a result of a deficient superoxide-synthesis, frequent and recurrent infections caused by rare pathogens have been described. We present the case of a 28-year old patient who has been diagnosed with IBD at the age of 2 years. He showed recurrent liver abscesses and the picture of a chronic IBD.

Methods:  Clinical and laboratory data was obtained and endoscopic, radiologic and histologic examinations, tests for granulocytic functions as well as a genetic analysis were performed. Literature of the PubMed database and recent literature were analyzed.

Case:  Under immunosuppressive therapy, with TNF -blocker Adalimumab followed by therapy with integrin-receptor antagonist Vedolizumab, the patient developed recurrent abscesses of the liver. Those were the result of infection with a sensitive Staphylococcus aureus strain. Colonoscopy showed stenosis of the rectum and some inflammatory activity. Intestinal symptoms were unresponsive to all therapies for IBD. Furthermore, there was a presence of active acne and recurrent liver abscesses due to bacteria not typical for intestinal infections. Consequently, we considered a granulocyte dysfunction as the underlying cause. Diagnosis of a chronic granulomatous disease was confirmed by flow cytometry and oxidative burst test. Genetic analysis showed a homozygote mutation of the p47phox (NCF1) gene located on chromosome 7, which represents the most common autosomal recessive form with 20 - 25 % of cases.

Results:  In light of recent literature, this case report shows that chronic granulomatous disease should be considered as a differential diagnosis to therapy refractory IBD. This is the case, especially in young patients, when recurrent bacterial lesions caused by intestine-atypical pathogens appear.

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[慢性肉芽肿病作为炎性肠病的罕见鉴别诊断]。
背景:慢性肉芽肿病是一种罕见的疾病,在德国的患病率约为150例。模仿慢性炎症性肠病(IBD)的肠道表现仅在少数病例中被描述。由于缺乏超氧化物合成,由罕见病原体引起的频繁和复发性感染已被描述。我们提出了一个28岁的病人,在2岁时被诊断出患有IBD。他表现为复发性肝脓肿和慢性IBD的图片。方法:收集临床和实验室资料,进行内窥镜、放射学和组织学检查、粒细胞功能检查和遗传分析。对PubMed数据库的文献和近期文献进行分析。病例:在免疫抑制治疗下,使用TNF -阻滞剂阿达木单抗,然后使用整合素受体拮抗剂韦多利单抗,患者出现复发性肝脓肿。这些都是感染了敏感的金黄色葡萄球菌菌株的结果。结肠镜检查显示直肠狭窄和一些炎症活动。肠道症状对IBD的所有治疗均无反应。此外,还有活动性痤疮和复发性肝脓肿,这是由肠道感染不常见的细菌引起的。因此,我们认为粒细胞功能障碍是潜在的原因。通过流式细胞术和氧化爆破试验证实慢性肉芽肿病的诊断。遗传分析显示,p47phox (NCF1)基因位于7号染色体上,是最常见的常染色体隐性突变形式,占20 - 25%。结果:根据最近的文献,本病例报告显示慢性肉芽肿病应被视为治疗难治性IBD的鉴别诊断。当出现由肠道非典型病原体引起的复发性细菌病变时,尤其在年轻患者中就是这种情况。
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来源期刊
Zeitschrift fur Gastroenterologie
Zeitschrift fur Gastroenterologie 医学-胃肠肝病学
CiteScore
1.40
自引率
15.40%
发文量
562
审稿时长
6-12 weeks
期刊介绍: Die Zeitschrift für Gastroenterologie ist seit über 50 Jahren die führende deutsche Fachzeitschrift auf dem Gebiet der Gastroenterologie. Sie richtet sich an Gastroenterologen und alle anderen gastroenterologisch interessierten Ärzte. Als offizielles Organ der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten sowie der Österreichischen Gesellschaft für Gastroenterologie und Hepatologie informiert sie zuverlässig und aktuell über die wichtigen Neuerungen und Entwicklungen in der Gastroenterologie.
期刊最新文献
Mirikizumab for the treatment of chronic antibiotic-refractory pouchitis. Palliative treatment of malignant intestinal obstruction with EUS-guided ileosigmoidostomy - a case report. [Clinical Ultrasound (ClinUS) - Concepts and Controversies]. [Position paper of the Society for Paediatric Gastroenterology and Nutrition (GPGE) on the off-label use of biologics and signal inhibitors in children and adolescents with IBD that have already been approved for adults]. [Correction: Position paper of the Society for Paediatric Gastroenterology and Nutrition (GPGE) on the off-label use of biologics and signal inhibitors in children and adolescents with IBD that have already been approved for adults].
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