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Mucocele of the appendix due to endometriosis: A rare case report

机译:子宫内膜异位症引起的阑尾黏液囊肿:罕见病例报告

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摘要

Mucocele of the appendix due to endometriosis is extremely rare, and there are only 10 previously reported cases in the English literature. We report a case of mucocele of the appendix due to endometriosis and provide the first review of the literature. A 43-year-old woman was admitted to the hospital because of recurrent right lower abdominal pain during her menstrual periods. Colonoscopy revealed submucosal tumor-like elevations of the appendiceal orifice. Computed tomography and magnetic resonance imaging of the abdomen suggested cystic lesions near the appendix. Consequently, mucocele of the appendix was suspected preoperatively. An open ileocecal resection was performed. Multiple cystic lesions were observed around the appendix. The cystic lesions contained mucus. Histopathological examination was consistent with a mucocele of the appendix due to endometriosis. The postoperative course was uneventful. We present the first review of the literature to clarify the clinical features.
机译:由于子宫内膜异位引起的阑尾黏液囊肿极为罕见,英语文献中只有10例以前报道过的病例。我们报告一例由于子宫内膜异位引起的阑尾黏液囊肿,并提供了有关文献的第一篇综述。一名43岁的妇女因月经期间右下腹反复发作而入院。结肠镜检查显示阑尾孔的粘膜下肿瘤样升高。腹部计算机断层扫描和磁共振成像提示阑尾附近有囊性病变。因此,术前怀疑阑尾黏液囊肿。进行开放性回盲肠切除术。在阑尾周围观察到多个囊性病变。囊性病变含有粘液。由于子宫内膜异位症,组织病理学检查与阑尾黏液囊肿一致。术后过程很顺利。我们目前对文献进行首次综述以阐明临床特征。

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