Al-Obaidi Hasan, Al-Obaidi Mustafa, Moliya Pratiksha, Harb Hussein, Nawras Yusuf, Merza Nooraldin
Internal Medicine, Jamaica Hospital Medical Center, New York, USA.
Internal Medicine, Lund University, Lund, SWE.
Cureus. 2024 Dec 12;16(12):e75587. doi: 10.7759/cureus.75587. eCollection 2024 Dec.
The association between primary sclerosing cholangitis (PSC) and microscopic colitis (MC) has been explored in limited studies, suggesting potential shared pathophysiological mechanisms. This systematic review aimed to investigate this relationship by analyzing studies identified through comprehensive searches in PubMed, Embase, and the Cochrane Library. Two studies met the inclusion criteria: a case series of 12 patients and a case report, collectively analyzing 13 cases. The case series revealed that 75% of MC diagnoses occurred after PSC, with many cases being asymptomatic, suggesting potential underdiagnosis. The case report described a patient with collagenous colitis who developed severe PSC complications, underscoring the bidirectional relationship and clinical impact of these conditions. Both studies highlighted immune dysregulation, genetic predisposition (HLA-DR3, HLA-DRw52a), and alterations in gut flora as shared mechanisms. These findings emphasize the importance of increased clinical vigilance, early diagnosis, and management of MC in PSC patients. Further research is needed to validate these associations, evaluate routine screening, and explore therapeutic approaches.
原发性硬化性胆管炎(PSC)与显微镜下结肠炎(MC)之间的关联已在有限的研究中进行了探索,提示可能存在共同的病理生理机制。本系统评价旨在通过分析在PubMed、Embase和Cochrane图书馆全面检索所确定的研究来调查这种关系。两项研究符合纳入标准:一项包含12例患者的病例系列研究和一项病例报告,共分析了13例病例。病例系列研究显示,75%的MC诊断发生在PSC之后,许多病例无症状,提示可能存在漏诊。病例报告描述了一名患有胶原性结肠炎的患者出现了严重的PSC并发症,强调了这些疾病的双向关系和临床影响。两项研究均强调免疫失调、遗传易感性(HLA-DR3、HLA-DRw52a)以及肠道菌群改变是共同机制。这些发现强调了提高临床警惕性、对PSC患者进行MC早期诊断和管理的重要性。需要进一步研究来验证这些关联、评估常规筛查并探索治疗方法。