Early and late outcomes of congenital biliary dilatation in pediatric patients.

IF 1 4区 医学 Q3 PEDIATRICS
Yoshiaki Takahashi, Takashi Kobayashi, Yoshiaki Kinoshita, Yuhki Arai, Toshiyuki Ohyama, Naoki Yokota, Yu Sugai, Shoichi Takano
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Abstract

Background: This study aimed to reveal the early and late postoperative complications and outcomes after surgery for congenital biliary dilatation (CBD) by reviewing cases over the past 40 years.

Methods: We retrospectively evaluated 59 patients with CBD who underwent radical surgery for complications and outcomes, based on medical records. Early complications were defined as those requiring treatment within 5 years of the initial operation. Late complications were defined as those treated more than 5 years later.

Results: The median age at the first surgery was 37 months. Regarding biliary reconstruction, 54 of the 59 patients (91.5%) underwent hepaticojejunostomy. Although three patients underwent cholecystoduodenostomy and one patient underwent hepaticoduodenostomy, all were converted to hepaticojejunostomy after a median of 12.5 years. One patient developed synchronous biliary carcinoma and underwent pancreaticoduodenectomy. Early complications occurred in seven patients with 10 events (surgical site infection, n = 3 bile leakage, n = 3; ileus, n = 3; bile duct obstruction, n = 1 and intussusception, n = 1). Late complications occurred in nine patients with 12 events (ileus, n = 3; anastomotic stricture, n = 3; hepatolithiasis, n = 3; asynchronous biliary carcinoma, n = 2; pancreatolithiasis, n = 1). Two of the three patients with hepatolithiasis underwent hepatectomy refractory to the endoscopic approach. Two patients developed asynchronous biliary carcinoma at 34 and 13 years after last operation; both ultimately died of the carcinoma. Only 35 patients (61.4%) underwent a follow-up examination. A total of 11 female patients (45.8%) eventually married, and all successfully gave birth.

Conclusion: Although the long-term prognosis is excellent with complete cyst excision and hepaticojejunostomy, we emphasize the importance of long-term follow-up.

小儿先天性胆道扩张的早期和晚期疗效。
背景:本研究旨在通过回顾过去40年的病例,揭示先天性胆道扩张(CBD)手术后早期和晚期的并发症及结果:本研究旨在通过回顾过去 40 年的病例,揭示先天性胆道扩张(CBD)术后早期和晚期的并发症及治疗效果:我们根据病历回顾性评估了59例接受根治手术的CBD患者的并发症和治疗效果。早期并发症是指在初次手术后 5 年内需要治疗的并发症。晚期并发症是指超过5年后才接受治疗的并发症:首次手术的中位年龄为 37 个月。关于胆道重建,59 位患者中有 54 位(91.5%)接受了肝空肠吻合术。虽然有三名患者接受了胆囊十二指肠造口术,一名患者接受了肝十二指肠造口术,但所有患者都在中位 12.5 年后转为肝空肠造口术。一名患者出现同步胆道癌,接受了胰十二指肠切除术。七名患者出现了早期并发症,共 10 例(手术部位感染,3 例;胆汁渗漏,3 例;回肠梗阻,3 例;胆管梗阻,1 例;肠套叠,1 例)。9 名患者出现了晚期并发症,共 12 例(回肠炎,3 例;吻合口狭窄,3 例;肝结石,3 例;非同步胆管癌,2 例;胰腺结石,1 例)。三名肝结石患者中有两名接受了肝切除术,但内镜方法无效。两名患者分别在上次手术后 34 年和 13 年患上非同步胆管癌,最终均死于胆管癌。只有 35 名患者(61.4%)接受了随访检查。共有 11 名女性患者(45.8%)最终结婚,并且都成功生育:尽管完全切除囊肿和肝空肠吻合术的长期预后良好,但我们强调长期随访的重要性。
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
Pediatrics International
Pediatrics International 医学-小儿科
CiteScore
2.00
自引率
7.10%
发文量
519
审稿时长
12 months
期刊介绍: Publishing articles of scientific excellence in pediatrics and child health delivery, Pediatrics International aims to encourage those involved in the research, practice and delivery of child health to share their experiences, ideas and achievements. Formerly Acta Paediatrica Japonica, the change in name in 1999 to Pediatrics International, reflects the Journal''s international status both in readership and contributions (approximately 45% of articles published are from non-Japanese authors). The Editors continue their strong commitment to the sharing of scientific information for the benefit of children everywhere. Pediatrics International opens the door to all authors throughout the world. Manuscripts are judged by two experts solely upon the basis of their contribution of original data, original ideas and their presentation.
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