Department of Pediatric Urology, Hospital "Prof. Dr. Juan P. Garrahan", Buenos Aires, Argentina.
Department of Pediatric Urology, Hospital "Prof. Dr. Juan P. Garrahan", Buenos Aires, Argentina.
Urology. 2020 Sep;143:261. doi: 10.1016/j.urology.2020.06.003. Epub 2020 Jun 18.
Reninoma, or juxtaglomerular cell tumor, is a benign neoplasm which causes severe hypertension with elevated plasma renin activity. Usually, it is well localized on computed tomography scan or magnetic resonance images, and complete resection of the tumor with renal function preservation is the optimal treatment. To describe the technique of a transperitoneal nephron-sparing laparoscopic surgery in a pediatric patient.
Describe the technique of a minimally invasive nephron-sparing surgery for resection of a reninoma tumor in a child.
In a 14-year-old girl with history of severe high blood pressure, ultrasound detected a hypoechoic lesion in right kidney. Angio computed tomography scan confirmed a 20-mm diameter lesion in the anterior surface of the lower pole of right kidney and also informed a lower pole renal artery. Transperitoneal laparoscopic approach was performed using 4 ports. After mobilization of the colon, Gerota's fascia was opened and the tumor identified. Both polar and principal renal arteries were dissected and secured with vessel loops. The tumor was resected using an ultrasonic energy device. Selective clamping of the lower pole renal artery was performed during 8 minutes. The transected renal surface was closed with two continuous barbed sutures and the tumor was removed using a handmade endobag. Perirenal drainage was left for 4 days, there were no perioperative complications and the patient was discharged 2 days after surgery. Pathology confirmed typical reninoma immunohistochemical features. Blood pressure and plasma renin levels returned to normal. Postsurgical scintigraphy informed 40% differential function of the right kidney.
Reninoma is a benign renal tumor and because of its nature and localization, minimally invasive nephron-sparing surgery should be considered. Strategic planning of the surgery based on preoperative images is essential. If vessel clamping is imperative, minimizing ischemia time and/or selective clamping, when possible, help preserve renal function.
嗜铬细胞瘤,又称肾小球旁细胞瘤,是一种良性肿瘤,可导致肾素活性升高的严重高血压。通常,它在计算机断层扫描或磁共振成像上很好定位,保留肾功能的肿瘤完全切除术是最佳治疗方法。本文描述了一例儿童患者经腹腔途径保留肾单位的腹腔镜手术技术。
描述一例儿童肾素瘤肿瘤经微创保留肾单位手术切除的技术。
一名 14 岁女孩有严重高血压病史,超声检查发现右肾低回声病变。血管计算机断层扫描证实右肾下极前表面有一个 20 毫米直径的病变,并且告知下极肾动脉。采用经腹腔腹腔镜入路,使用 4 个端口。结肠游离后,打开 Gerota 筋膜,识别肿瘤。游离并夹闭肾极和主肾动脉,用血管套环固定。使用超声能量装置切除肿瘤。选择性夹闭下极肾动脉 8 分钟。用双道连续倒刺缝线闭合肾断面,用手工制作的 EndoBAG 取出肿瘤。术后留置肾周引流管 4 天,无围手术期并发症,术后 2 天出院。病理证实为典型的嗜铬细胞瘤免疫组化特征。血压和血浆肾素水平恢复正常。术后闪烁显像提示右肾功能 40%。
嗜铬细胞瘤是一种良性肾肿瘤,由于其性质和位置,应考虑微创保留肾单位手术。基于术前图像的手术策略规划至关重要。如果必须夹闭血管,应尽量减少缺血时间和/或选择性夹闭,以帮助保留肾功能。