儿童壶腹周围十二指肠重复囊肿的诊断和手术治疗:附病例报告

Y. Sokolov, G. Tumanyan, A. Efremenkov, Zh.R. Omarova, O. Y. Koshurnikov, Alaniia A. Gogichaeva
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引用次数: 0

摘要

背景:慢性十二指肠梗阻的梗阻性变异可能由先天性畸形引起,如罕见的壶腹周围十二指肠重复囊肿。这种胃肠道重复的定位是最罕见的,在国内文献中没有描述。目的:本研究旨在介绍小儿壶腹周围十二指肠重复囊肿的治疗经验。病例报告:2007年至2022年间,7名儿童壶腹周围十二指肠重复囊肿接受了手术。所有患者均出现持续腹痛、食物呕吐和胆汁分泌。2例患儿复发性胰腺炎,1例患儿因高位肠梗阻、胆道梗阻在其他医院多次手术。另一家医院的一名患者怀疑腹部囊肿,并对该儿童进行了腹腔镜探查,但未发现形成。对这些儿童进行了超声、胃十二指肠镜检查、计算机断层扫描和磁共振成像。超声检查显示一个直径达4厘米的双壁蠕动性囊性形成。胃十二指肠镜检查显示在十二指肠第二部分的主要十二指肠乳头区域形成。这种结构覆盖了三分之二的肠腔,几乎完全封闭。磁共振胰胆管造影明确了十二指肠复制与胆管和胰管的关系:在两个儿童中怀疑存在这种关系。所有患者均行经十二指肠广泛切除壶腹周围十二指肠重复囊肿;其中4例采用腹腔镜手术。无术中及术后并发症发生。组织学检查显示所有病例均有重复。孩子们在第1112天出院。随访3个月和10年,无并发症发生。结论:壶腹周围十二指肠重复囊肿可能是慢性十二指肠梗阻的一个原因。经十二指肠切除壶腹周围十二指肠重复囊肿是最佳的治疗方法,该手术可在腹腔镜下进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostics and surgical management of periampullary duodenal duplication cysts in children: a report of cases
BACKGROUND: Obstructive variants of chronic duodenal obstruction may be caused by congenital malformations, such as rare periampullary duodenal duplication cysts. This localization of gastrointestinal duplications is the rarest and is not described in the domestic literature. AIM: This study aimed to present the experience of the management of periampullary duodenal duplication cysts in children. CASES REPORT: Seven children with periampullary duodenal duplication cysts underwent surgery between 2007 and 2022. All patients suffered from prolonged abdominal pain, vomiting of food, and bile. Two children had recurrent pancreatitis, and one child underwent repeated operations for high intestinal obstruction and biliary obstruction in other hospitals. An abdominal cyst was suspected in one patient at another hospital, and the child underwent exploratory laparoscopy, but no formation was found. Ultrasound, gastroduodenoscopy, computed tomography, and magnetic resonance imaging were performed on these children. Ultrasound examination showed a peristaltic cystic formation up to 4 cm in diameter with a double wall. Gastroduodenoscopy showed formation in the second portion of the duodenum in the region of the major duodenal papilla. This formation covers the intestinal lumen by two-thirds and up to nearly complete obturation. The relationship between duodenal duplication and the bile and pancreatic ducts was clarified on magnetic resonance cholangiopancreatography: the relationship was suspected in two children. All patients underwent wide transduodenal excision of periampullary duodenal duplication cyst; in four cases, laparoscopic access was used. No intra- and postoperative complications occurred. Histological examination revealed true duplications in all cases. The children were discharged on days 1112. In the follow-up after 3 months and 10 years, no complications were noted. CONCLUSIONS: Periampullary duodenal duplication cysts can be a cause of chronic duodenal obstruction. Transduodenal excision of periampullary duodenal duplication cysts is the optimal treatment, and this operation can be performed laparoscopically.
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