一例13岁患者的肠系膜静脉肌内膜增生与炎症性肠病相似。

JPGN reports Pub Date : 2024-10-07 eCollection Date: 2024-11-01 DOI:10.1002/jpr3.12130
Dua Abuquteish, Rose Chami, Govind B Chavhan, Thomas Walters, Iram Siddiqui
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摘要

特发性肠系膜静脉肌内膜增生(IMHMV)是一种罕见的成人疾病,通常与炎症性肠病(IBD)相似。我们报告了第一例继发于IMHMV的肠缺血,在患有唐氏综合征的儿童患者中表现为IBD。慢性肠道缺血在儿童中很少见,本病例强调当组织病理学提示时,需要在鉴别时考虑这一点。这些患者的临床表现和结肠镜检查可能与IBD相似。粘膜活检未显示IBD的典型特征。相反,可出现不同程度的粘膜改变,如固有层小毛细血管扩张、水肿和早期纤维化。这些变化实际上可能代表早期慢性缺血。这些发现提示血管成像和全层活检来评估粘膜下和浆膜下的大血管,因为在IMHMV中,结肠壁和肠系膜的中、大口径静脉受到影响。
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Myointimal hyperplasia of the mesenteric veins mimicking inflammatory bowel disease in a 13-year-old patient.

Idiopathic myointimal hyperplasia of the mesenteric veins (IMHMV) is a rare entity reported in adults, frequently mimicking inflammatory bowel disease (IBD). We report the first case of intestinal ischemia secondary to IMHMV presenting as IBD in a pediatric patient with Down syndrome. Chronic intestinal ischemia is rare in children, and this case emphasizes the need to consider this in the differential, when histopathology is suggestive. Clinical findings and colonoscopy in these patients may mimic IBD. The mucosal biopsies do not show classic features of IBD. Instead, there can be variable extent of mucosal changes such as dilated small capillaries in the lamina propria, edema, and early fibrosis. These changes may in fact represent early chronic ischemia. These findings should alert for vascular imaging and a full-thickness biopsy to assess submucosal and subserosal larger vessels since medium- and large-caliber veins in the colonic wall and mesentery are affected in IMHMV.

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