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胆囊重复畸形合并胆总管囊肿:一种罕见的情况。

Gall Bladder Duplication with Choledochal Cyst: A Rare Entity.

作者信息

Sharma Rahul Deo, Sushma Achugatla, Singh Surendra, Tewari Shruti, Redkar Rajeev

机构信息

Department of Paediatric Surgery, Lilavati Hospital and Research Centre, Mumbai, Maharashtra, India.

出版信息

J Indian Assoc Pediatr Surg. 2023 Jul-Aug;28(4):325-327. doi: 10.4103/jiaps.jiaps_20_23. Epub 2023 Jul 11.

Abstract

A 4-year-old male child presented with complaints of abdominal pain and vomiting along with yellowish discoloration of the eyes. Investigations were suggestive of acute pancreatitis and double gall bladder (GB) with dilated common bile duct (CBD) with intraluminal calculi and Type II choledochal cyst. He underwent surgical resection of double GB with dilated CBD with hepatico-docho-jejunostomy. On follow-up, the patient was asymptomatic. Our case highlights the importance of preoperative diagnosis to deal with increased operative difficulty and complications.

摘要

一名4岁男童出现腹痛、呕吐以及眼睛发黄的症状。检查提示为急性胰腺炎、双胆囊伴胆总管扩张并管腔内结石以及II型胆总管囊肿。他接受了双胆囊及扩张胆总管切除并肝管-胆总管-空肠吻合术。随访时,患者无症状。我们的病例强调了术前诊断对于应对手术难度增加和并发症的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/698e/10455702/869fd86894c0/JIAPS-28-325-g001.jpg

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