| Literature DB >> 32114370 |
Francesco Motolese1, Mariagrazia Rossi2, Emma Gangemi3, Anna Bersano4, Emma Scelzo4, Vincenzo Di Lazzaro2, Fioravante Capone2.
Abstract
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a common cause of inherited stroke in young adults. CADASIL causes extensive white matter T2 hyperintensities at brain MRI, in particular involving anterior-temporal lobes and external capsules; usually, there is no spinal cord involvement. Since CADASIL clinical spectrum is heterogeneous and MRI findings are sometimes not specific, Multiple Sclerosis (MS) represents a frequent CADASIL misdiagnosis. Herein, we describe the case of a 48-year-old man affected by CADASIL and referred to our clinic with an initial diagnosis of secondary progressive MS because of diffuse leukoencephalopathy and spinal cord lesions at MRI.Entities:
Keywords: CADASIL; Leukoencephalopathy; Multiple Sclerosis; Spinal cord lesion
Mesh:
Year: 2020 PMID: 32114370 DOI: 10.1016/j.msard.2020.102014
Source DB: PubMed Journal: Mult Scler Relat Disord ISSN: 2211-0348 Impact factor: 4.339