Kulkarni B, Oak S N, Karmarkar S J, Desai A P, Deshmukh S S
Department of Paediatric Surgery, L T M G Hospital, Sion, Mumbai.
J Postgrad Med. 1995 Apr-Jun;41(2):49-51.
Duplications of the alimentary tract are of a great rarity, particularly so in the rectum. Because of its rarity, the difficulty of making a correct diagnosis and of selection of proper approach for treatment, this entity bears a special significance. The present case report deals with a female newborn who presented with imperforate anus and a rectovestibular fistula and a mass prolapsing at the introitus. Complete excision of the mass was carried out through the perineal approach and the child then underwent, a PSARP for the correction of the rectal anomaly. Histology confirmed the mass to be a rectal duplication.
消化道重复畸形极为罕见,在直肠部位更是如此。由于其罕见性,做出正确诊断以及选择合适的治疗方法存在困难,因此这一病症具有特殊意义。本病例报告涉及一名女性新生儿,她患有肛门闭锁、直肠前庭瘘,并且在阴道口有肿物脱出。通过会阴途径对肿物进行了完整切除,随后患儿接受了经会阴肛门直肠成形术以矫正直肠畸形。组织学检查证实该肿物为直肠重复畸形。