A man in his fifties with lymphoma, vomiting and diarrhoea.

IF 1.2 Q2 MEDICINE, GENERAL & INTERNAL
Tidsskrift for Den Norske Laegeforening Pub Date : 2025-05-12 Print Date: 2025-05-13 DOI:10.4045/tidsskr.24.0605
Jakob Lillemoen Drivenes, Anders Lillemoen Drivenes, Randi Haukaas Bjerkreim, Istvan Pregun, Tor Jacob Eide, Otto Emil Nyquist
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引用次数: 0

Abstract

Background: Diagnosing immunosuppressed patients who present with fever and gastrointestinal symptoms can be particularly challenging for clinicians.

Case presentation: We report the case of a man in his fifties who developed severe enterocolitis, immunosuppression and protein loss following treatment with rituximab and bendamustine. His medical history included recurrent iridocyclitis and small lymphocytic lymphoma, with subsequent identification of necrobiotic xanthogranuloma, prompting the initiation of chemoimmunotherapy. The patient initially presented with fever, vomiting and diarrhoea. Despite receiving appropriate medical care, he experienced recurrent infections and significant gastrointestinal distress, necessitating an extended hospital stay that involved interdisciplinary collaboration. Initial investigations indicated cytomegalovirus (CMV) reactivation, which was initially misinterpreted as CMV colitis. However, further biopsies revealed no classic CMV lesions, and comprehensive gastroenterological and microbiological evaluations ruled out infectious causes. This led to a diagnosis of rituximab-induced enterocolitis, a rare adverse effect of the treatment, confirmed by re-examination of the biopsies. Despite attempts to manage the condition with corticosteroids and TNF inhibitors, the patient ultimately succumbed to complications, including severe infections and renal failure.

Interpretation: This case underscores the critical need to recognise rituximab-induced enterocolitis, especially in patients presenting with unexplained gastrointestinal symptoms during therapy. Timely diagnosis and intervention may improve patient outcomes, highlighting the necessity for vigilant monitoring of such patients.

一个五十多岁的男人,患有淋巴瘤,呕吐和腹泻。
背景:对临床医生来说,诊断伴有发热和胃肠道症状的免疫抑制患者尤其具有挑战性。病例介绍:我们报告一例50多岁的男性,在接受利妥昔单抗和苯达莫司汀治疗后,出现了严重的小肠结肠炎,免疫抑制和蛋白质丢失。他的病史包括复发性虹膜睫状体炎和小淋巴细胞淋巴瘤,随后发现坏死性黄色肉芽肿,促使他开始化疗免疫治疗。病人最初表现为发烧、呕吐和腹泻。尽管接受了适当的医疗护理,但他仍经历了反复感染和严重的胃肠不适,需要延长住院时间,涉及跨学科合作。初步调查显示巨细胞病毒(CMV)再激活,最初被误解为巨细胞病毒结肠炎。然而,进一步的活检显示没有典型的巨细胞病毒病变,综合胃肠病学和微生物学评估排除了感染原因。这导致诊断为利妥昔单抗诱导的小肠结肠炎,这是一种罕见的治疗不良反应,通过重新检查活检证实。尽管试图用皮质类固醇和肿瘤坏死因子抑制剂来控制病情,但患者最终还是死于并发症,包括严重感染和肾衰竭。解释:该病例强调了识别利妥昔单抗诱导的小肠结肠炎的关键必要性,特别是在治疗期间出现无法解释的胃肠道症状的患者。及时的诊断和干预可以改善患者的预后,强调了对这类患者进行警惕监测的必要性。
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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来源期刊
Tidsskrift for Den Norske Laegeforening
Tidsskrift for Den Norske Laegeforening MEDICINE, GENERAL & INTERNAL-
CiteScore
0.60
自引率
18.20%
发文量
593
审稿时长
28 weeks
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