Patent Urachus with Patent Vitellointestinal Duct: A Rare Simultaneous Occurrence.

Shreyas Dudhani, Keerthana Bachagala, Bijay Kumar Suman, Rashi Rashi, Amit Kumar Sinha
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Abstract

Abstract: A large number of congenital anomalies often involve the umbilicus. This is a report of two such anomalies together in an infant. The child had a mass protruding from the umbilicus since birth. The urachus was noted to be patent on voiding cystourethrogram. On exploration, a patent vitellointestinal duct was also noted. Resection and anastomosis was done for the vitellointestinal duct, and the urachus was excised close to the dome of the bladder. Histopathological examination confirmed a tube lined by intestinal epithelium and the urachal remnant showing a dense fibrous tube-like structure. The omphalo-mesenteric vessels are located between the urachus and the patent vitellointestinal duct, and care should be taken while incising or dissecting in this region to prevent bleeding.

尿道闭锁合并腹腔肠管闭锁:罕见的同时发生
摘要:大量先天性畸形常常涉及脐部。本病例是一名婴儿同时患有两种此类畸形的报告。患儿自出生起就有一个肿块从脐部突出。排尿膀胱尿道造影显示尿道通畅。探查时还发现了一条通畅的葡萄肠管。对玻璃体肠管进行了切除和吻合,并在靠近膀胱穹隆处切除了尿道。组织病理学检查证实,尿管内衬为肠上皮,尿道残端显示出致密的纤维管状结构。输尿管-肠系膜血管位于尿道和输尿管之间,在这一区域切开或解剖时应小心谨慎,以防出血。
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