Pudhiavan Arunachalam, Agrawal Alka, Chaudhari Sangit, Shukla Anil
Department of Radiodiagnosis, M.G.M.M.C. & M.Y. Hospital, Indore, India.
J Radiol Case Rep. 2013 Apr 1;7(4):1-9. doi: 10.3941/jrcr.v7i4.1338. Print 2013 Apr.
Cerebrotendinous xanthomatosis (CTX), also known as Van Bogaert-Scherer-Epstein disease is a rare autosomal recessive genetic disorder of the lipid metabolism. To date, there are less than 300 cases reported worldwide. We present a case of a 30 year old male who presented with mental retardation and swelling of ankles, with the a spectrum of CTX imaging findings. Imaging studies were performed which included plain X-ray, Ultrasound(US) and Magnetic Resonance Imaging(MRI) of both the brain and ankles. These pointed towards the diagnosis of CTX with the entire spectrum of findings which was confirmed with biopsy and laboratory findings. CTX is a potentially treatable condition with replacement therapy, and hence early diagnosis before neurological deterioration is important. This is aided by the imaging findings which are conclusive forte diagnosis of CTX.
脑腱黄瘤病(CTX),也称为范博加尔特 - 谢勒 - 爱泼斯坦病,是一种罕见的常染色体隐性脂质代谢遗传疾病。迄今为止,全球报告的病例不到300例。我们报告一例30岁男性,表现为智力发育迟缓及脚踝肿胀,并伴有一系列CTX影像学表现。进行了包括脑部和脚踝的X线平片、超声(US)及磁共振成像(MRI)在内的影像学检查。这些检查结果指向CTX的诊断,活检和实验室检查结果证实了全部检查结果。CTX通过替代疗法有潜在的可治疗性,因此在神经功能恶化之前早期诊断很重要。影像学检查结果有助于CTX的确切诊断。