依多沙班诱导的小肠结肠炎:第一例报告显示明显的内窥镜和组织学特征

IF 1.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
DEN open Pub Date : 2025-08-01 DOI:10.1002/deo2.70142
Katsuya Endo, Jun Yamada, Tomofumi Katayama, Yuki Yoshino, Daisuke Fukushi, Akinobu Koiwai, Takayuki Kogure, Morihisa Hirota, Kennichi Satoh
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引用次数: 0

摘要

直接口服抗凝剂(DOACs),包括依多沙班,广泛用于房颤和静脉血栓栓塞的卒中预防。虽然胃肠道出血和腹泻是公认的不良反应,但doac诱导的小肠结肠炎尚未被确定为一个独特的临床实体。我们报告了首例依多沙班诱导的肠结肠炎,患者为一名75岁的女性,她在开始使用依多沙班5天后出现血性腹泻和厌食症。回肠结肠镜检查显示回肠末端散在性红肿、溃疡和糜烂,伴从横结肠到直肠的弥漫性水肿和粘膜下出血。组织病理学显示回肠绒毛萎缩,淋巴扩张,淋巴细胞浸润为主,伴隐窝萎缩,粘膜水肿,结肠出血。这些发现与感染性、缺血性、血管性或炎症性肠病不一致,提示药物引起的病因。考虑到急性发作和独特的内窥镜和组织病理学发现,怀疑为依多沙班诱导的小肠结肠炎。停用依多沙班3天后症状消失,3个月后随访回肠结肠镜检查显示粘膜完全愈合。根据临床过程,我们最终诊断为依多沙班性肠炎。由于DOACs的广泛使用,类似病例可能未被充分认识,因为这些患者的不明原因血性腹泻通常缺乏详细的内镜评估。需要进一步的病例报告和研究来确定doac诱发的肠炎是一个独特的临床实体。该病例是识别doac诱导的小肠结肠炎的关键第一步,并强调了临床医生提高认识的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Edoxaban-induced enterocolitis: The first case report demonstrating distinct endoscopic and histological features

Edoxaban-induced enterocolitis: The first case report demonstrating distinct endoscopic and histological features

Direct oral anticoagulants (DOACs), including edoxaban, are widely used for stroke prevention in atrial fibrillation and venous thromboembolism. While gastrointestinal bleeding and diarrhea are recognized adverse effects, DOAC-induced enterocolitis has not been established as a distinct clinical entity. We report the first case of edoxaban-induced enterocolitis in a 75-year-old woman who developed bloody diarrhea and anorexia five days after starting edoxaban. Ileocolonoscopy revealed scattered redness, ulcers, and erosions in the terminal ileum, with diffuse edema and submucosal bleeding from the transverse colon to the rectum. Histopathology showed villous atrophy, lymphatic dilation, and lymphocyte-predominant infiltration in the ileum, along with crypt atrophy, mucosal edema, and hemorrhages in the colon. These findings were inconsistent with infectious, ischemic, vasculitic, or inflammatory bowel diseases, suggesting a drug-induced etiology. Given the acute onset and unique endoscopic and histopathological findings, edoxaban-induced enterocolitis was suspected. The patient's symptoms resolved three days after discontinuing edoxaban, and a follow-up ileocolonoscopy after 3 months showed complete mucosal healing. In accordance with the clinical course, we ultimately diagnosed this case as edoxaban-induced enteritis. Given the widespread use of DOACs, similar cases may be underrecognized, as unexplained bloody diarrhea in these patients often lacks detailed endoscopic evaluation. Further case reports and studies are needed to establish DOAC-induced enteritis as a distinct clinical entity. This case serves as a critical first step in recognizing DOAC-induced enterocolitis and highlights the need for increased awareness among clinicians.

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