ⅠС型胆总管囊肿患儿的诊断和治疗特点

A. Sinitsyn, A. I. Perepelkin, G. A. Kopan
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引用次数: 0

摘要

胆总管囊肿是肝外和/或肝内胆管的先天性囊性扩张。对这种病变的诊断和治疗策略的选择往往会造成困难。本研究对一例胆总管囊肿病例进行了回顾性分析,该患儿年仅 2 岁,症状为反复黄疸、胆管炎和胰腺炎,在准备根治手术期间需要进行腹腔镜胆囊造口术和胆管造影。患儿再次入住小儿外科,主诉体温高达 39°C,再次出现周期性腹痛、恶心、巩膜和皮肤黄疸加重。实验室和超声波检查显示患者患有胆道和胰腺高血压。诊断为胆总管囊肿、胆汁淤积综合征、急性胆囊-胰腺炎。根据现有的临床症状以及实验室和超声波检查数据,紧急实施了腹腔镜胆囊造口术。在保守治疗的背景下,腹腔镜胆囊造口术后 2 天内,临床、实验室和对照超声检查显示,胆道和胰腺高血压均已停止。患儿在没有额外麻醉的情况下通过胆囊造口术进行了胆管造影,结果显示肝总管和胆总管呈纺锤形扩张。在腹腔镜胆囊造口术的背景下,经过两周的药物治疗后,患儿接受了胆总管囊肿切除术和胆囊切除术,并在Roux-en-Y环路上进行了肝肠吻合术。术后恢复顺利。24 个月内未发现其他不适或并发症。在报告的病例中,复发性梗阻性黄疸是由胆总管囊肿引起的。腹腔镜胆囊造口术能够快速、成功地缓解胆道高压,为根治性手术治疗做好准备,并通过胆囊造口术安全地进行胆管造影。根据Roux-en-Y方法进行的肝肠吻合术是治疗胆总管囊肿的有效手术方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of diagnosis and treatment of a child with choledochal cyst IС type
Choledochal cysts are congenital cystic dilatations of the extrahepatic and/or intrahepatic bile ducts. Diagnosis and choice of treatment tactics for this pathology often cause difficulties. A case report of a choledochal cyst in a 2-year-old patient with symptoms of recurrent jaundice, cholangitis, and pancreatitis, which required laparoscopic cholecystostomy and cholangiography during preparation for radical surgery, was retrospectively analyzed. The child was re-admitted to the pediatric surgical department with complaints of hyperthermia up to 39°C, resumption of periodic abdominal pain, nausea, and increased icterus of the sclera and skin. Laboratory and ultrasound examination indicated biliary and pancreatic hypertension. Choledochal cyst, cholestasis syndrome, acute cholecystopancreatitis was diagnosed. Owing to the existing clinical symptoms and laboratory and ultrasound data, laparoscopic cholecystostomy was urgently performed. Against the background of conservative therapy, within 2 days after laparoscopic cholecystostomy, clinically, laboratory and according to control ultrasound examination, biliary and pancreatic hypertension were stopped. The child underwent cholangiography through a cholecystostomy without additional anesthesia, which revealed a fusiform dilatation of the common hepatic and bile ducts. After 2 weeks of drug treatment against the background of laparoscopic cholecystostomy, the child underwent excision of the common bile duct cyst, and cholecystectomy with hepatic enteroanastomosis on a Roux-en-Y loop. The postoperative period was smooth. No other complaints or complications were noted within 24 months. In the reported case, recurrent obstructive jaundice was caused by a choledochal cyst. Laparoscopic cholecystostomy enabled the quick and successful relief of biliary hypertension, preparation of the patient for radical surgical treatment, and safe informative cholangiography through cholecystostomy. Hepatic enteroanastomosis with a disconnected loop according to Roux-en-Y was an effective surgical treatment method for choledochal cyst.
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