Cutaneous Crohn's disease after proctocolectomy for medically refractory colonic Crohn's disease: a case series and review of the literature.

IF 2.1 Q3 GASTROENTEROLOGY & HEPATOLOGY Annals of Gastroenterology Pub Date : 2023-07-01 Epub Date: 2023-05-30 DOI:10.20524/aog.2023.0811
Sandra Naffouj, Gabriel E Marrero-Rivera, Johan Nordenstam, Kyle T Amber, Itishree Trivedi
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Abstract

Background: Cutaneous Crohn's disease (CCD), also known as metastatic Crohn's disease (CD), is one of the rarest and most challenging cutaneous manifestations of CD. It is characterized by non-caseating granulomatous inflammation of the skin at sites that are non-contiguous with the gastrointestinal (GI) tract. Diagnosis of CCD needs a high clinical suspicion since morphological presentation varies widely and lacks an apparent correlation to the activity of the luminal CD. The onset of CCD in patients without active GI CD is a particularly understudied phenomenon.

Methods: We present a case series of a unique patient group who developed CCD while in remission from a luminal CD perspective, mainly after a proctocolectomy for Crohn's colitis. We also provide a literature review and summary of case reports of CCD after proctocolectomy.

Results: Our 4 adult patients diagnosed with CCD after proctocolectomy presented herein, were successfully treated with high-dose corticosteroids, followed by biologic therapy. Furthermore, a comprehensive review of CCD is provided regarding its pathogenesis, clinical presentation, differential diagnosis, and the evidence behind the available treatments.

Conclusions: CCD should be considered in any CD patient presenting with skin lesions regardless of their disease activity status and history of proctocolectomy. The treatment remains challenging; biologics remain the cornerstone and a multidisciplinary approach is recommended. Larger randomized clinical trials are essential to determine the optimal treatment protocol and to improve outcomes.

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医学难治性结肠克罗恩病顺产术后的皮肤克罗恩病:病例系列和文献综述。
背景:皮肤性克罗恩病(CCD),也称为转移性克罗恩氏病(CD),是CD最罕见、最具挑战性的皮肤表现之一。其特征是在与胃肠道不相连的部位出现非干酪样肉芽肿性皮肤炎症。CCD的诊断需要高度的临床怀疑,因为形态学表现差异很大,并且与管腔CD的活性缺乏明显的相关性。在没有活动性胃肠道CD的患者中CCD的发作是一个特别缺乏研究的现象。方法:我们介绍了一个独特的患者组的一系列病例,从管腔CD的角度来看,他们在病情缓解时出现CCD,主要是在克罗恩结肠炎顺产切除术后。我们还提供了文献回顾和总结的CCD病例报告后顺产。结果:我们的4名成人患者在顺产结肠切除术后被诊断为CCD,他们成功地接受了高剂量皮质类固醇治疗,然后进行了生物治疗。此外,对CCD的发病机制、临床表现、鉴别诊断以及现有治疗方法背后的证据进行了全面的综述。结论:任何CD患者,无论其疾病活动状态和顺产切除史如何,都应考虑CCD。治疗仍然具有挑战性;生物制剂仍然是基石,建议采用多学科方法。更大规模的随机临床试验对于确定最佳治疗方案和改善结果至关重要。
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来源期刊
Annals of Gastroenterology
Annals of Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.30
自引率
0.00%
发文量
58
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