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先天性门体分流致高胰岛素血症性低血糖行活体肝移植治疗。

Living Donor Liver Transplantation for Congenital Portosystemic Shunt Presenting With Hyperinsulinemic Hypoglycemia.

机构信息

Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Department of Pediatric Surgery, Kyoto University Hospital, Kyoto, Japan.

出版信息

Pediatr Transplant. 2024 Nov;28(7):e14871. doi: 10.1111/petr.14871.

Abstract

BACKGROUND

A congenital portosystemic shunt (CPSS) is defined as abnormal vascular communications between the portal vein and the systemic vein. Encephalopathy, hepatopulmonary syndrome, and portopulmonary hypertension are manifestations in patients with CPSS. Hyperinsulinemic hypoglycemia is also one of the manifestations of CPSS. Hyperinsulinemic hypoglycemia secondary to CPSS is caused by a lack of hepatic first-pass elimination of insulin, which is secreted from pancreatic beta cells.

CASE PRESENTATION

A 7-month-old boy had hypergalactosemia detected by newborn mass screening. Enhanced abdominal computed tomography showed the absence of the portal vein trunk and extrahepatic portosystemic communication between the superior mesenteric vein and the inferior vena cava. He had suffered from uncontrollable hyperinsulinemic hypoglycemia under protein and lactose restriction. We performed living donor liver transplantation (LDLT) using a left lateral segment graft from his father. The postoperative course was uneventful and the hypoglycemic attacks disappeared.

CONCLUSION

We believe that uncontrolled hyperinsulinemic hypoglycemia secondary to CPSS is an indication of LDLT.

摘要

背景

先天性门体分流(CPSS)定义为门静脉和体循环静脉之间的异常血管交通。脑病、肝肺综合征和门脉高血压是 CPSS 患者的表现。高胰岛素血症性低血糖也是 CPSS 的表现之一。CPSS 引起的高胰岛素血症性低血糖是由于胰腺β细胞分泌的胰岛素缺乏肝首过消除所致。

病例介绍

一名 7 个月大的男孩在新生儿大规模筛查中发现高半乳糖血症。增强腹部 CT 显示门静脉主干缺失,肠系膜上静脉与下腔静脉之间存在肝外门体分流。他在限制蛋白质和乳糖后仍出现无法控制的高胰岛素血症性低血糖。我们使用来自他父亲的左外侧段移植物进行活体供肝移植(LDLT)。术后过程顺利,低血糖发作消失。

结论

我们认为,CPSS 引起的无法控制的高胰岛素血症性低血糖是 LDLT 的指征。

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