以Wunderlich综合征为表现的大肾血管平滑肌脂肪瘤的治疗结果——来自三级中心的经验。

IF 1.9 Q3 ONCOLOGY
Atanu Kumar Pal, Sidhartha Kalra, Sreerag Kodakkattil Sreenivasan, Lalgudi Narayanan Dorairajan, Ramanitharan Manikandan, Shailendra Kumar Sah
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引用次数: 1

摘要

肾血管平滑肌脂肪瘤是一种罕见的良性混合间充质肿瘤,由厚壁血管、平滑肌和成熟脂肪组织组成。这些肿瘤中有20%与结节性硬化症有关。Wunderlich综合征(WS)是一种急性非创伤性自发性肾周出血,可表现为大血管平滑肌脂肪瘤。本研究评估了2019年1月至2021年12月期间急诊就诊的8例肾血管平滑肌脂肪瘤合并WS患者的表现、处理和并发症。临床表现为腹部疼痛、可触及肿块、血尿及肾周间隙出血。评估了人口统计学数据、出现时的症状、合并症、血流动力学参数、与结节硬化的关系、输血要求、血管栓塞的需要、手术处理、Clavien-Dindo并发症、住院时间和30天再入院率。平均发病年龄为38岁。8例患者中女性5例(62.5%),男性3例(37.5%)。2例(25%)患者有结节性硬化症合并血管平滑肌脂肪瘤,3例(37.5%)患者有低血压。平均填充细胞输注量为3个单位,平均肿瘤大小为7.85 cm (3.5-25 cm)。其中3例(37.5%)需要紧急血管栓塞以防止失血。1例(33%)接受急诊开放式部分肾切除术的患者栓塞失败,1例(33%)患者出现栓塞后综合征。共有6例患者接受了选择性手术,其中4例接受了部分肾切除术(腹腔镜- 1,机器人- 1,开放式- 2),2例接受了开放式肾切除术。3例患者出现Clavien-Dindo并发症(1级,n = 2, IIIA级,n = 2)。WS是大型血管平滑肌脂肪瘤患者中一种罕见的危及生命的并发症。明智的优化、血管栓塞和及时的手术干预将有助于获得更好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Management Outcomes of Large Renal Angiomyolipoma Presenting with Wunderlich Syndrome-Experience from a Tertiary Center.

Management Outcomes of Large Renal Angiomyolipoma Presenting with Wunderlich Syndrome-Experience from a Tertiary Center.

Management Outcomes of Large Renal Angiomyolipoma Presenting with Wunderlich Syndrome-Experience from a Tertiary Center.
Renal angiomyolipoma is an uncommon, benign-mixed mesenchymal tumor consisting of thick-walled blood vessels, smooth muscles, and mature adipose tissues. Twenty percent of these tumors are associated with tuberous sclerosis. Wunderlich syndrome (WS), an acute nontraumatic spontaneous perirenal hemorrhage, can be a presentation of large angiomyolipoma. This study evaluated the presentation, management, and complications of renal angiomyolipoma with WS in eight patients who presented to the emergency department between January 2019 and December 2021. The presenting symptoms included flank pain, palpable mass, hematuria, and bleeding in the perinephric space on computerized tomography. Demographic data, symptoms at presentation, comorbidities, hemodynamic parameters, the association with tuberous sclerosis, transfusion requirements, need for angioembolization, surgical management, Clavien–Dindo complication, duration of hospital stay, and 30-day readmission rates were evaluated. The mean age of presentation was 38 years. Of the eight patients, five (62.5%) were females and 3(37.5%) were males. Two (25%) patients had tuberous sclerosis with angiomyolipoma, and three (37.5%) patients presented with hypotension. The mean packed cell transfusion was three units, and the mean tumor size was 7.85 cm (3.5–25 cm). Three of them (37.5%) required emergency angioembolization to prevent exsanguination. Embolization was unsuccessful in one patient (33%) who underwent emergency open partial nephrectomy, and one (33%) patient developed post-embolization syndrome. A total of six patients underwent elective surgery—four underwent partial nephrectomy (laparoscopic - 1, robotic - 1, open - 2) and two underwent open nephrectomy. Three patients encountered Clavien–Dindo complications (Grade 1, n = 2 and IIIA, n = 2). WS is a rare, life-threatening complication in patients with large angiomyolipoma. Judicious optimization, angioembolization, and prompt surgical intervention will help deliver better outcomes.
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