Shah Adil A, Luca Dragos C, Kane Timothy D, Petrosyan Mikael
Department of Surgery, Howard University College of Medicine, Washington, District of Columbia, USA.
Department of General and Thoracic Pediatric Surgery, Children's National Health System, Washington, District of Columbia, USA.
BMJ Case Rep. 2018 May 18;2018:bcr-2018-224550. doi: 10.1136/bcr-2018-224550.
Myoid angioendothelioma are rare and benign vascular tumours of the spleen. Radiographic evaluation and diagnosis is often challenging and subjecting tissue samples to immuhistochemical analysis is often required to make a definitive diagnosis. Myoidangioendotheliomas can be managed with open or laparoscopic splenectomy with minimal risk of recurrent disease. Herein, we present a case of a myoid angioendothelioma in a patient with stage IV Wilms' tumour.
肌样血管内皮瘤是脾脏罕见的良性血管肿瘤。影像学评估和诊断往往具有挑战性，通常需要对组织样本进行免疫组织化学分析才能做出明确诊断。肌样血管内皮瘤可通过开放性或腹腔镜脾切除术进行治疗，疾病复发风险极小。在此，我们报告一例患有IV期威尔姆斯瘤患者的肌样血管内皮瘤病例。
