Wala Samantha J, Beebe Morgan, Warren Patrick, Kallash Mahmoud, Nathan Jaimie, Rasmussen Sara
Department of Abdominal Transplantation & Hepatopancreatobiliary Surgery, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH, 43205, USA.
Department of Nephrology, Nationwide Children's Hospital, Columbus, OH, USA.
J Med Case Rep. 2025 Apr 29;19(1):196. doi: 10.1186/s13256-025-05208-z.
Renal artery stenosis due to neurofibromatosis type 1 is a known important source of secondary renovascular hypertension in pediatric patients. There are no guidelines on the management of renal artery stenosis in children, and the utility of stents and bypass grafting is limited given small patient size. Renal autotransplant to treat renal artery stenosis in a small pediatric patient may be a viable alternative for treatment and spare the need for nephrectomy.
In this article, we present a case of renal autotransplant in a 6-year-old, 15.8 kg Nepali patient with neurofibromatosis type 1 with refractory hypertension and high-grade stenosis of the proximal right main renal artery. The patient underwent balloon angioplasty, which failed to dilate the stenosis. He later developed hypertensive urgency and required admission to the pediatric intensive care unit. The patient was not a candidate for repeat angioplasty given the length of the stenotic segment and its tortuosity. Blood pressure was unable to be controlled on multiple antihypertensive agents and the patient eventually developed hypertensive urgency. Therefore, a renal autotransplant of the right kidney was performed after multidisciplinary evaluation. The right renal artery ostium had significant hypertrophied intima involving 50% of its circumference. The kidney was procured in the same fashion as a living kidney donor nephrectomy. The kidney was mobilized in situ, and heparin was administered. The renal artery and renal vein were divided with surgical staplers. The kidney was removed from the patient and moved to the back table. On the back table, the organ was flushed with cold organ preservation solution and vessels inspected. The diseased portion of the right renal artery was resected to the location of no gross intimal thickening. It was judged that there was adequate length of the healthy artery remaining to allow safe reimplantation. The renal artery and vein were reimplanted to the abdominal aorta and inferior vena cava, respectively. The patient tolerated the surgery well, and 2 years postoperatively, he only requires one antihypertensive medication.
Nephrectomy may be favored over renal autotransplant in small pediatric patients due to technical difficulties associated with autotransplant. We demonstrate significant clinical improvement in blood pressure control in a 15.8 kg, 6-year-old pediatric patient after renal autotransplant.
1型神经纤维瘤病所致肾动脉狭窄是小儿继发性肾血管性高血压的一个重要已知病因。目前尚无关于儿童肾动脉狭窄治疗的指南,鉴于患儿体型较小,支架置入和旁路移植术的应用有限。对于治疗小儿患者的肾动脉狭窄,自体肾移植可能是一种可行的替代治疗方法,可避免肾切除术。
在本文中,我们介绍了一例6岁、体重15.8千克的尼泊尔1型神经纤维瘤病患者,该患者患有难治性高血压和右肾主肾动脉近端重度狭窄,接受了自体肾移植手术。患者接受了球囊血管成形术,但未能扩张狭窄部位。随后他出现高血压急症,需要入住儿科重症监护病房。鉴于狭窄段的长度及其迂曲情况,患者不适合再次进行血管成形术。多种降压药物均无法控制血压,患者最终发展为高血压急症。因此,在多学科评估后,对患者实施了右肾自体肾移植手术。右肾动脉开口处内膜明显肥厚,累及圆周的50%。肾脏的获取方式与活体肾供体肾切除术相同。在原位游离肾脏,并给予肝素。用手术吻合器切断肾动脉和肾静脉。将肾脏从患者体内取出并移至后手术台。在后手术台上,用冷器官保存液冲洗器官并检查血管。将右肾动脉的病变部分切除至无明显内膜增厚的位置。经判断,剩余健康动脉的长度足够,可安全进行再植入。将肾动脉和肾静脉分别重新植入腹主动脉和下腔静脉。患者对手术耐受性良好,术后2年,他仅需服用一种降压药物。
由于自体肾移植存在技术困难,小儿患者可能更倾向于肾切除术。我们证明,一名体重15.8千克、6岁的小儿患者在接受自体肾移植术后,血压控制有显著的临床改善。