Colitis associated with persistent drug-induced immune dysregulation.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-12-01 Epub Date: 2024-08-09 DOI:10.1007/s00428-024-03878-6
Johanna Köhler, Randolf Hammerl, Daniel M Mayer, Johannes Fessler, Cord Langner
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Abstract

Adverse drug reactions frequently involve the gastrointestinal tract. We present two cases of colitis that occurred months to years after chemotherapy and autologous stem cell transplantation for the treatment of lymphoma. Laboratory tests revealed altered immune status with decreased CD4/CD8 ratio and hypogammaglobinemia (in one patient). The patients had no history of inflammatory bowel disease or immunodeficiency. Biopsies showed chronic active colitis with crypt architectural distortion, erosions, and ulcers as well as pyloric gland metaplasia and loss of plasma cells (in one patient, respectively). Colitis appeared to be related to lymphoma therapy, but could not be attributed to a distinct drug or infectious agent, suggesting the concept of persistent immune dysregulation driving mucosal inflammation. Hence, we suggest "immune dysregulation-associated colitis" (ID-colitis) as an umbrella term for cases of chronic colitis, in which immune dysfunction is evident from blood samples or clinical information and inflammatory bowel disease has been ruled out.

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结肠炎与药物引起的持续免疫失调有关。
药物不良反应经常涉及胃肠道。我们介绍了两例在化疗和自体干细胞移植治疗淋巴瘤数月至数年后发生的结肠炎病例。实验室检查显示,患者的免疫状态发生了改变,CD4/CD8比值下降,并出现低丙种球蛋白血症(一名患者)。患者没有炎症性肠病或免疫缺陷病史。活组织检查显示,慢性活动性结肠炎伴有隐窝结构变形、糜烂和溃疡,以及幽门腺变性和浆细胞丢失(分别发生在一名患者身上)。结肠炎似乎与淋巴瘤治疗有关,但不能归因于某种药物或感染性病原体,这表明持续性免疫调节失调是导致粘膜炎症的原因。因此,我们建议将 "免疫调节失调相关性结肠炎"(ID-colitis)作为慢性结肠炎病例的总称,在这些病例中,从血液样本或临床信息中可以明显看出免疫功能失调,并且已经排除了炎症性肠病的可能性。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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