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胶原性袋炎

Collagenous pouchitis.

作者信息

Shen B, Bennett A E, Fazio V W, Sherman K K, Sun J, Remzi F H, Lashner B A

机构信息

Center for Inflammatory Bowel Disease, The Cleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH 44195, USA.

出版信息

Dig Liver Dis. 2006 Sep;38(9):704-9. doi: 10.1016/j.dld.2006.05.022. Epub 2006 Jun 27.

Abstract

Collagenous colitis is characterised by watery diarrhoea, normal colonic mucosa on endoscopy, diffuse colitis with surface epithelial injury, and a distinctive thickening of the subepithelial collagen table on histology. Some patients can develop medically refractory collagenous colitis, in which case they may require surgical intervention. This is the first report of collagenous pouchitis in a collagenous colitis patient with proctocolectomy and ileal pouch-anal anastomosis. A patient with medically refractory collagenous colitis who underwent a total proctocolectomy and ileal pouch-anal anastomosis was sequentially evaluated with an endoscopy and histology of the colon, distal small intestine, and ileal pouch. A 58-year-old female had a 10-year history of collagenous colitis before having a total proctocolectomy and ileal pouch-anal anastomosis for medically refractory disease. The histologic features of collagenous colitis were present in all colon and rectum biopsy or resection specimens, but were absent in the distal ileum specimen. The post-operative course was complicated by persistent increase of stool frequency, abdominal cramps, and incontinence. A pouch endoscopy was performed 3 years after ileal pouch-anal anastomosis which showed the histologic features of collagenous colitis in the ileal pouch, collagenous pouchitis, while the pre-pouch neo-terminal ileum had no pathologic changes. After antibiotic therapy, the histologic changes of collagenous pouchitis resolved. This is the first reported case of collagenous pouchitis. Since the abnormal collagen table and its associated features were only present in the pouch and absent in the neo-terminal ileum, and the patient had histologic improvement after antibiotic therapy, it would suggest that faecal stasis and bacterial load may play a role in the pathogenesis.

摘要

胶原性结肠炎的特征为水样腹泻、内镜检查显示结肠黏膜正常、弥漫性结肠炎伴表面上皮损伤以及组织学上上皮下胶原板显著增厚。一些患者会发展为药物难治性胶原性结肠炎,在这种情况下可能需要手术干预。这是首例关于一名接受全直肠结肠切除术和回肠贮袋肛管吻合术的胶原性结肠炎患者发生胶原性贮袋炎的报告。一名药物难治性胶原性结肠炎患者接受了全直肠结肠切除术和回肠贮袋肛管吻合术,随后依次接受了结肠、远端小肠和回肠贮袋的内镜检查及组织学检查。一名58岁女性在因药物难治性疾病接受全直肠结肠切除术和回肠贮袋肛管吻合术之前,有10年的胶原性结肠炎病史。所有结肠和直肠活检或切除标本均呈现胶原性结肠炎的组织学特征,但远端回肠标本未出现该特征。术后病程出现大便次数持续增加、腹部绞痛和失禁等并发症。回肠贮袋肛管吻合术后3年进行了贮袋内镜检查,结果显示回肠贮袋存在胶原性结肠炎的组织学特征,即胶原性贮袋炎,而贮袋前新的终末回肠无病理改变。抗生素治疗后,胶原性贮袋炎的组织学改变消失。这是首例报告的胶原性贮袋炎病例。由于异常的胶原板及其相关特征仅存在于贮袋中,而在新的终末回肠中不存在,且患者在抗生素治疗后组织学得到改善,这表明粪便淤滞和细菌负荷可能在发病机制中起作用。

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