青少年溃疡性结肠炎的鉴别诊断:慢性肉芽肿性疾病需要特别注意。

Daniel Kotlarz, Odul Egritas Gurkan, Zehra Sule Haskologlu, Ozgur Ekinci, Aysel Aksu Unlusoy, Neslihan Gürcan Kaya, Jacek Puchalka, Cristoph Klein, Buket Dalgic
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引用次数: 18

摘要

慢性肉芽肿病(CGD)是一种原发性免疫缺陷,通常在5岁以下诊断出来(95%),在成年期很少见。儿童期CGD可能表现为炎症性肠病(IBD)。如果没有适当的诊断,这些患者可能会作为IBD监测多年;有些人甚至可能被认为是类固醇抵抗性溃疡性结肠炎(UC),最终需要进行结肠切除术。在这个病例报告中,我们描述了一个患者,他被随访多年为UC,随后接受了结肠切除术,但最终在成年时被诊断为原发性免疫缺陷。
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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Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention.

Chronic granulomatous disease (CGD) is a primary immune deficiency that is commonly diagnosed under the age of 5 years (95%) and is rarely seen in adulthood. CGD may manifest as inflammatory bowel disease (IBD) in childhood. Without proper diagnosis, these patients may be monitored for years as IBD; some may even be regarded as steroid-resistant ulcerative colitis (UC) and end up having a colectomy. In this case report, we described a patient who had been followed-up for years as UC and subsequently underwent colectomy, but was finally diagnosed in adulthood as primary immune deficiency.

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