Unmasking Amoebiasis: An Unexpected Cause of Colitis in a Non-endemic Region.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-06-27 eCollection Date: 2025-06-01 DOI:10.7759/cureus.86877
Vikash S Sagar, Nauman Nauman, Gayathri Jayakumar, Bismah Kazi
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Abstract

Amoebic colitis is a common mimic of inflammatory bowel disease (IBD), primarily encountered in developing countries. We present a case of a 73-year-old British male with no travel history to any amoebic endemic regions, who presented with a three-month history of per rectal (PR) bleeding, diarrhoea, and a positive faecal immunochemical test (FIT). Prior to this, he reported no history of experiencing any gastrointestinal symptoms. Colonoscopy revealed patchy pan-colitis, most marked in the ascending colon, and histology confirmed chronic inflammation. A diagnosis of IBD was made, and the patient was started on corticosteroids and 5-aminosalicylates (5-ASA). He subsequently presented to the emergency department (ED) with worsening symptoms and rising inflammatory markers. Flexible sigmoidoscopy showed progression of inflammation, and despite treatment with intravenous corticosteroids and infliximab, a tumour necrosis factor-alpha (TNF-α) inhibitor, there was no improvement. Cross-sectional imaging performed due to new-onset breathlessness during this admission identified multiple hepatic abscesses and a superior mesenteric vein thrombus. Immunosuppression was stopped, and broad-spectrum antibiotics were initiated. Liver biopsy showed inflammatory cells, but no microorganisms were seen on cultures. Due to treatment-refractory colitis and contraindications to further immunosuppression, the patient underwent a laparoscopic subtotal colectomy with end ileostomy. Histology of the resected bowel was not in keeping with IBD, prompting re-evaluation of the initial biopsies taken from the colonoscopy at first presentation. On re-examination, amoebic-like trophozoites were seen, and the diagnosis of amoebic colitis was confirmed following review by a tertiary centre for specialist infectious disease and gastrointestinal pathology. This case highlights the need for a broad differential when managing treatment-refractory colitis, particularly in non-endemic regions, where the index of suspicion for amoebic colitis is low, and the risk of misdiagnosis is high.

揭露阿米巴病:在非流行地区结肠炎的一个意想不到的原因。
阿米巴结肠炎是一种常见的模拟炎症性肠病(IBD),主要发生在发展中国家。我们报告了一例73岁的英国男性,没有任何阿米巴流行地区的旅行史,他表现为三个月的直肠(PR)出血,腹泻和粪便免疫化学试验(FIT)阳性。在此之前,他没有任何胃肠道症状的病史。结肠镜检查显示斑片状泛结肠炎,以升结肠最为明显,组织学证实为慢性炎症。诊断为IBD,患者开始使用皮质类固醇和5-氨基水杨酸(5-ASA)。随后,他出现在急诊科(ED),症状恶化,炎症标志物上升。柔性乙状结肠镜检查显示炎症进展,尽管静脉注射皮质类固醇和英夫利昔单抗(一种肿瘤坏死因子-α (TNF-α)抑制剂)治疗,但没有改善。在入院期间,由于新发呼吸困难,横断面成像发现多发肝脓肿和肠系膜上静脉血栓。停止免疫抑制,开始使用广谱抗生素。肝活检显示炎症细胞,但培养未见微生物。由于难治性结肠炎和进一步免疫抑制的禁忌症,患者接受了腹腔镜结肠次全切除术并末端回肠造口术。切除的肠的组织学与IBD不一致,促使在第一次出现时重新评估结肠镜检查的初始活检。复查时发现阿米巴样滋养体,经专科传染病和胃肠病理学三级中心复查后确诊为阿米巴结肠炎。这一病例强调了在处理难治性结肠炎时需要进行广泛的区分,特别是在阿米巴结肠炎怀疑指数低、误诊风险高的非流行地区。
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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