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一种罕见的消化道畸形——尾肠囊肿:病例报告

A rare malformation of the alimentary tract, tailgut cyst : a case report.

作者信息

Ozturk Hulya, Dagistan Emine, Ozturk Hayrettin

机构信息

Abant Izzet Baysal University, Medical School, Pediatric Surgery, Bolu, Turkey.

Abant Izzet Baysal University, Medical School, Radiodiagnostic, Bolu, Turkey.

出版信息

Acta Gastroenterol Belg. 2018 Oct-Dec;81(4):528-530.

Abstract

Tailgut cyst (cystic hamartoma) is a rare congenital pathology that arises -from post-natal primitive gut remnants in the retrorectal-presacral space. Because of the rarity of the lesion and the variability of the anatomical position, its diagnosis and surgical treatment are often difficult. Complete surgical excision of the multilocular and multicystic process prevents recurrent draining sinuses and eliminates the possibility of malignant change. We describe a case in which a tailgut cyst localized in the retrorectal and presacral space was characterized by abscess, repeated urinary tract infection, and rectal pain.

摘要

尾肠囊肿(囊性错构瘤)是一种罕见的先天性病变,起源于出生后直肠后骶前间隙的原始肠道残余物。由于该病变罕见且解剖位置多变,其诊断和手术治疗往往具有挑战性。对多房性和多囊性病变进行完整的手术切除可防止反复出现引流窦,并消除恶变的可能性。我们描述了一例位于直肠后和骶前间隙的尾肠囊肿病例,其特征为脓肿、反复尿路感染和直肠疼痛。

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