Proximal Roux-en-Y Limb Intussusception After Pediatric Living Donor Liver Transplantation for Biliary Atresia: A Rare Surgical Emergency.

IF 1.4 4区 医学 Q3 PEDIATRICS
Peng Cai, Seisuke Sakamoto, Hajime Uchida, Chanokkamol Kiataramkul, Ayane Oshiro, Masato Kojima, Ryuji Komine, Yusuke Yanagi, Akinari Fukuda, Mureo Kasahara
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引用次数: 0

Abstract

Background: Intussusception of the Roux-en-Y limb after pediatric liver transplantation (LT) is an extremely rare but potentially life-threatening complication. Altered anatomy, postoperative adhesions, and disrupted intestinal motility create a unique pathophysiological environment, which may delay diagnosis and increase morbidity.

Methods: We retrospectively analyzed a patient with acute intestinal obstruction after living donor liver transplantation. Clinical presentation, laboratory findings, imaging results, intraoperative observations, surgical management, and outcomes were reviewed. The potential pathogenesis was explored in relation to factors such as Roux-en-Y reconstruction, graft-to-recipient size ratio, and postoperative adhesive disease.

Results: The patient presented with fever and melena. Laboratory evaluation revealed leukocytosis and severe anemia. Computed tomography demonstrated small bowel intussusception with obstruction. Emergency laparotomy identified intussusception of the proximal Roux limb near the biliary-enteric anastomosis. Manual reduction was unsuccessful, necessitating segmental resection without reconstruction of a new Roux limb. Extensive intra-abdominal adhesions were noted. Postoperative recovery was uneventful, and graft function remained stable.

Conclusions: Intussusception of the Roux-en-Y limb following pediatric living donor liver transplantation is a complex surgical emergency. This case demonstrates that in the transplant population, symptoms such as fever and melena should trigger immediate cross-sectional imaging to rule out mechanical obstruction. The management strategy must be aggressive yet conservative regarding anatomical disruption. As the population of long-term pediatric transplant survivors grows, recognizing these distinct mechanistic patterns is essential for reducing morbidity and mortality.

小儿活体肝移植治疗胆道闭锁后近端Roux-en-Y肢体肠套叠:一种罕见的外科急诊。
背景:小儿肝移植(LT)后Roux-en-Y肢体肠套叠是一种极其罕见但可能危及生命的并发症。解剖结构改变、术后粘连和肠道运动紊乱造成了独特的病理生理环境,这可能会延迟诊断并增加发病率。方法:回顾性分析1例活体供肝移植术后急性肠梗阻患者。我们回顾了临床表现、实验室检查、影像学结果、术中观察、手术处理和结果。探讨其潜在的发病机制与Roux-en-Y重建、移植物与受体大小比、术后粘连疾病等因素的关系。结果:患者表现为发热、黑黑。实验室检查显示白细胞增多和严重贫血。计算机断层扫描显示小肠肠套叠伴梗阻。急诊剖腹探查发现胆肠吻合口附近Roux肢体近端肠套叠。手工复位不成功,需要节段性切除而不重建新的Roux肢体。注意到广泛的腹内粘连。术后恢复平稳,移植物功能保持稳定。结论:儿童活体肝移植术后Roux-en-Y肢体肠套叠是一种复杂的外科急诊。本病例表明,在移植人群中,发烧和黑黑等症状应立即触发横断成像以排除机械阻塞。对于解剖破坏,治疗策略必须积极而保守。随着长期儿童移植幸存者人数的增长,认识到这些独特的机制模式对于降低发病率和死亡率至关重要。
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
Pediatric Transplantation
Pediatric Transplantation 医学-小儿科
CiteScore
2.90
自引率
15.40%
发文量
216
审稿时长
3-8 weeks
期刊介绍: The aim of Pediatric Transplantation is to publish original articles of the highest quality on clinical experience and basic research in transplantation of tissues and solid organs in infants, children and adolescents. The journal seeks to disseminate the latest information widely to all individuals involved in kidney, liver, heart, lung, intestine and stem cell (bone-marrow) transplantation. In addition, the journal publishes focused reviews on topics relevant to pediatric transplantation as well as timely editorial comment on controversial issues.
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