Delayed diagnosis of bronchobiliary fistula complicating a pediatric living donor liver transplantation: a case report.

Q4 Medicine
Korean Journal of Transplantation Pub Date : 2023-12-31 Epub Date: 2023-10-27 DOI:10.4285/kjt.23.0044
Vipul Gautam, Vikram Kumar, Shaleen Agarwal, Subhash Gupta
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引用次数: 0

Abstract

Bronchobiliary fistula (BBF) is a very rare condition in children. Only a few pediatric BBF cases have been reported, in the context of a ruptured hydatid cyst or liver abscess. BBF after living donor liver transplantation (LDLT) has not been reported in the pediatric literature. We report a 7-year-old female child with Wilson disease, who developed BBF post-LDLT. She had a clinically uneventful course in the immediate post-transplant period. She was readmitted on postoperative day (POD) 75 with a productive cough and respiratory difficulty, which was diagnosed as bilioptysis secondary to BBF. Endoscopic retrograde cholangiopancreaticography was attempted but failed. Exploratory laparotomy showed a fistula from the strictured biliary anastomotic site to the right thoracic cavity; it was excised, and a Roux-en-Y hepaticojejunostomy was performed. She tolerated the procedure well and remained clinically well on follow-up through POD 185. BBF is extremely rare in children. This is the first case report of BBF in a child following LDLT. BBF requires a high index of suspicion for a timely intervention to prevent subsequent complications.

儿童活体肝移植并发支气管胆道瘘的延迟诊断:一例报告。
支气管胆瘘(BBF)是一种非常罕见的儿童疾病。只有少数儿科BBF病例的报道,在破裂的棘球蚴囊肿或肝脓肿的背景下。活体供肝移植(LDLT)后的BBF尚未在儿科文献中报道。我们报告了一名患有Wilson病的7岁女童,她在LDLT后出现BBF。移植后不久,她的临床表现平平。术后第75天(POD),她因生产性咳嗽和呼吸困难再次入院,被诊断为BBF继发的胆汁溶解。曾尝试过内镜逆行胰胆管造影术,但失败了。剖腹探查显示从狭窄的胆道吻合口到右侧胸腔有瘘;将其切除并进行Roux-en-Y肝肠造口术。她对手术耐受性良好,并在POD 185的随访中保持良好的临床表现。BBF在儿童中极为罕见。这是LDLT后第一例儿童BBF病例报告。BBF需要高怀疑指数才能及时干预,以防止随后的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Korean Journal of Transplantation
Korean Journal of Transplantation Medicine-Transplantation
CiteScore
0.80
自引率
0.00%
发文量
32
审稿时长
24 weeks
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