Parente Fabienne, Vesnaver Matthew, Massie Rami, Baass Alexis
Department of Medical Biochemistry, Research Institute of McGill University Health Center (RI-MUHC), Centre for Translational Biology, Montreal, Quebec, Canada.
Department of Medical Biochemistry, Research Institute of McGill University Health Center (RI-MUHC), Centre for Translational Biology, Montreal, Quebec, Canada; Department of Experimental Medicine, McGill University, Montreal, Quebec, Canada.
J Clin Lipidol. 2016 Jul-Aug;10(4):1040-1044. doi: 10.1016/j.jacl.2016.05.001. Epub 2016 May 13.
Tendinous xanthomas are often thought to be pathognomonic for familial hypercholesterolemia. In this report, we present the case of a young man with a normal lipid profile and Achilles tendon xanthoma. Biochemical and genetic studies confirmed the diagnosis of cerebrotendinous xanthomatosis in this patient. Cerebrotendinous xanthomatosis is a rare autosomal recessive disease associated with xanthoma in tendons and the brain as well as progressive neurologic deficits. Unfortunately, this rare form of reversible dementia is thought to be underdiagnosed. Early diagnosis and treatment of this disease with chenodeoxycholic acid is essential and has been shown to greatly improve the patient's symptoms and prognosis.
腱黄瘤通常被认为是家族性高胆固醇血症的特征性表现。在本报告中,我们介绍了一名血脂谱正常但患有跟腱黄瘤的年轻男性病例。生化和基因研究证实该患者患有脑腱性黄瘤病。脑腱性黄瘤病是一种罕见的常染色体隐性疾病,与肌腱和脑部的黄瘤以及进行性神经功能缺损有关。不幸的是,这种罕见的可逆性痴呆形式被认为诊断不足。早期诊断并用鹅去氧胆酸治疗这种疾病至关重要,并且已证明可大大改善患者的症状和预后。