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Mucinous cystadenoma of the appendix with enterocutaneous fistula: a therapeutic dilemma

机译:阑尾粘液性囊腺瘤伴肠胃瘘:一种治疗难题

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Mucinous cystadenoma of appendix is a rare clinical entity with very few reported cases in the literature. Consensus on optimal surgical management has not been reached. We report the case of a 65-year-old female patient who presented with fistula over the right iliac fossa. Computed tomography (CT) of the abdomen suggested abscess of the parietal wall. Upon exploration, a mass was found to be arising from the tip of the retroperitoneal appendix and the retroperitoneum was studded with mucoid material. Appendectomy was carried out and final histopathology revealed mucinous cystadenoma with no evidence of malignancy. The patient was discharged uneventfully. The unusual presentation of this disease, as retroperitoneal psuedomyxoma without any intraperitoneal pathology, prompted us to report this case.
机译:阑尾粘液性膀胱腺瘤是一种罕见的临床实体,文献报道的病例很少。尚未就最佳手术管理达成共识。我们报道了一名65岁女性患者的病例,该患者在右窝上方出现瘘管。腹部计算机断层扫描(CT)提示壁壁脓肿。经探查,发现腹膜后阑尾有肿块,腹膜后覆盖有粘液样物质。进行了阑尾切除术,最终的组织病理学显示粘液性囊腺瘤,无恶性证据。病人出院很顺利。这种疾病的异常表现为腹膜后脓肿,而无腹膜内病理,促使我们报告此病例。

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