Ahsan M, Choudhury S, Razi R M, Verma D K
Dr Mainul Ahsan, Associate Professor, Department of Radiology & Imaging, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh; E-mail:
Mymensingh Med J. 2021 Jul;30(3):850-854.
Angiomyolipomas (AML) are benign tumor of kidney also referred as renal hamartoma composed of varying amounts of mature adipose tissue, smooth muscle, and blood vessels. It is seen in two distinct clinical forms, a sporadic (isolated) form and 55-80% seen in association with Tuberous sclerosis complex (TSC). If the lesion grows to a large size, a series of clinical manifestations and serious complications may occur. Here we present a case of 26 years lady who presented in the Department Radiology & Imaging of Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh with chief complaints of bilateral loin pain and occasional hematuria for 2 months. Ultrasound abdomen and contrast enhanced computed tomography shows bilateral renal angiomyolipoma (left>right). In order to look for tuberous sclerosis features, we followed her with plain computed tomography of head which shows subependymal calcifications.
血管平滑肌脂肪瘤(AML)是一种肾脏良性肿瘤,也被称为肾错构瘤,由不同比例的成熟脂肪组织、平滑肌和血管组成。它有两种不同的临床形式,一种是散发性(孤立性)形式,另一种是与结节性硬化症(TSC)相关,发生率为55%-80%。如果病变生长到很大尺寸,可能会出现一系列临床表现和严重并发症。在此,我们报告一例26岁女性患者,她因双侧腰痛和偶尔血尿2个月,就诊于孟加拉国达卡班加班德谢赫穆吉布医科大学(BSMMU)放射科和影像科。腹部超声和增强CT显示双侧肾血管平滑肌脂肪瘤(左侧>右侧)。为了寻找结节性硬化症的特征,我们对她进行了头部平扫CT检查,发现了室管膜下钙化。