胰肾同时移植后同种异体肾移植扭转:病例报告及文献复习。

Case Reports in Transplantation Pub Date : 2025-01-19 eCollection Date: 2025-01-01 DOI:10.1155/crit/2902758
Ayato Obana, Miho Akabane, Matthew Hamilton, Kejal Shah, Rithin Sai Punjala, Ashley Limkemann, Austin Schenk, Navdeep Singh, Amer Rajab, Ginny Bumgardner, Kenneth Washburn, Musab Alebrahim
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引用次数: 0

摘要

同种异体肾移植扭转(KAT)是一种罕见但严重的肾移植并发症,可导致急性缺血导致移植物丧失。本报告报告了一例腹腔胰肾同时移植(SPK) 9个月后KAT导致移植物丢失的病例,并回顾了以前的报道以确定潜在的高危特征。一位38岁女性继发于1型糖尿病的终末期肾脏疾病患者接受了腹腔内肠内引流SPK移植。移植后9个月,患者出现恶心、呕吐、严重腹痛、尿量减少和腹泻。超声检查显示中度肾积水,肾门无血流。剖腹探查发现一个坏死的同种异体肾移植在其血管蒂上逆时针旋转360°。尽管腐化,移植物显示没有活力的迹象,需要移植肾切除术。这个病例强调了KAT的罕见性和严重性,特别是在腹膜内肾移植中。患者的低体重指数(BMI) (23.4 kg/m2)、女性(骨盆较宽)和最小的腹腔粘连可能导致移植物移动性增加,易发生KAT。其他潜在的危险因素包括血管蒂延长和免疫抑制相关的粘连形成减少。KAT的非特异性表现强调了在移植物异常的情况下需要高度的临床怀疑和及时的超声评估。本报告强调了在评估KAT风险时考虑患者和移植物特异性因素的重要性,以及早期发现和干预以防止移植物丢失的关键性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kidney Allograft Torsion After Simultaneous Pancreas Kidney Transplantation: Case Report and Review of Literature.

Kidney allograft torsion (KAT) is a rare but critical complication of kidney transplantation that can lead to graft loss due to acute ischemia. This report presents a case of KAT resulting in graft loss 9 months following intraperitoneal simultaneous pancreas and kidney (SPK) transplant and reviews previous reports to identify potential high-risk features. A 38-year-old female with end-stage renal disease secondary to Type 1 diabetes mellitus underwent an intraperitoneal enteric drained SPK transplant. Nine months post-transplantation, she presented with nausea, vomiting, severe abdominal pain, decreased urine output, and diarrhea. An ultrasound showed moderate hydronephrosis and no blood flow to the renal hilum. Exploratory laparotomy revealed a necrotic renal allograft twisted 360° counterclockwise on its vascular pedicles. Despite detorsion, the graft showed no signs of viability, necessitating transplant nephrectomy. This case highlights the rarity and severity of KAT, particularly in intraperitoneal kidney transplants. The patient's low body mass index (BMI) (23.4 kg/m2), female sex (wider pelvis), and minimal intra-abdominal adhesions may have contributed to increased graft mobility, predisposing to KAT. Other potential risk factors include elongated vascular pedicle and immunosuppression-related reduced adhesion formation. The nonspecific presentation of KAT emphasizes the need for high clinical suspicion and prompt ultrasonographic evaluation in cases of graft abnormalities. This report underscores the importance of considering patient- and graft-specific factors in assessing KAT risk and the critical nature of early detection and intervention to prevent graft loss.

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