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腹膜后纤维化:输尿管和小肠梗阻的罕见病因。

Retroperitoneal fibrosis: a rare cause of both ureteral and small bowel obstruction.

作者信息

Aziz Faisal, Conjeevaram Srinivasulu, Phan Than

机构信息

Department of Surgery, New York Medical College, Munger Pavilion, Suite 211, Valhalla, NY 10595, USA.

出版信息

World J Gastroenterol. 2006 Nov 21;12(43):7061-3. doi: 10.3748/wjg.v12.i43.7061.

Abstract

Retroperitoneal fibrosis (RPF) is a rare condition of unclear etiology. It can cause ureteral obstruction. We present the unique case of a 54 years old female, who initially presented with spontaneous perforation of the cecum. Upon exploring the abdomen, the classical glistening white, unyielding retroperitoneal fibrosis was encountered. A right hemicolectomy was performed. Subsequently, the patient presented with bilateral ureteral obstruction, and later on with small bowel obstruction. Ureteral obstruction was treated with stents, and small bowel obstruction was treated with bypass. To our knowledge no case of idiopathic RPF presenting with features of both bilateral ureteral and small bowel obstruction has been reported in the literature.

摘要

腹膜后纤维化(RPF)是一种病因不明的罕见病症。它可导致输尿管梗阻。我们报告了一例独特的病例,一名54岁女性,最初表现为盲肠自发性穿孔。在探查腹部时,发现了典型的闪闪发光的白色、坚硬的腹膜后纤维化。进行了右半结肠切除术。随后,患者出现双侧输尿管梗阻,后来又出现小肠梗阻。输尿管梗阻采用支架治疗,小肠梗阻采用旁路手术治疗。据我们所知,文献中尚未报道过特发性RPF同时出现双侧输尿管和小肠梗阻特征的病例。

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