Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: An imaging mimic of multiple sclerosis: A report of two cases

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Abstract

Objective and Importance: To describe the imaging findings of two cases of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) mimicking multiple sclerosis. Clinical Presentation and Intervention: Two cases presenting with neurological signs and symptoms were referred for magnetic resonance imaging (MRI) evaluation of the brain. Case 1 was a 36-year-old female patient presenting with recurrent headaches and recent onset numbness in the fingers of the right hand. Neurological examination showed a mild sensory deficit in the right hand. Case 2 was a 31-year-old female patient presenting with attacks of right-sided numbness of the face and body. The neurological examination revealed a sensory loss in the face and brisk deep tendon reflexes. Routine MRI sequences showed two types of lesions in both cases: 'punctate' hyperintense lesions on T 2-weighted images (T2WI)/fluid-attenuated inversion recovery (FLAIR) images, hypointense on T1-weighted images (T 1WI) and 'diffuse' white matter lesions, hyperintense on T 2WI/FLAIR sequences and isointense to hypointense on T1WI. All lesions showed no contrast enhancement. Both cases were previously clinically and radiologically diagnosed as multiple sclerosis. There was a strong family history consistent with recurrent infarctions in other family members of both patients. Both cases were later diagnosed as CADASIL by skin biopsy/genetic linkage studies and follow-up. Conclusion: The cases showed that CADASIL causes stroke-like episodes in adults and can mimic multiple sclerosis on imaging. Clinical evaluation and MRI findings allow a differentiation of the two entities. Copyright © 2006 S. Karger AG.

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Pandey, T., & Abubacker, S. (2006). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: An imaging mimic of multiple sclerosis: A report of two cases. Medical Principles and Practice, 15(5), 391–395. https://doi.org/10.1159/000094276

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