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Acta Neurol Taiwan ; 24(1): 30-3, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26179688

RESUMO

PURPOSE: Relapsing polychondritis (RP) is a rare systemic autoimmune disease affecting cartilaginous and non-cartilaginous structures. Neurological involvement is rarer but results in profound disability. Early identification and treatment of underlying RP may promote neurological recovery. CASE REPORT: We illustrated a 53-year-old man diagnosed with dementia. Neuroimaging and cerebrospinal fluid studies disclosed meningoencephalitis. "Prominent ear sign" was evident on diffusion-weight magnetic resonance imaging. After glucocortisone administration, the improvement of clinical manifestations was closely correlated subsequent neuroimaging findings. CONCLUSION: The importance of better understanding of this disease in terms of the prevention of further tissue damage in patients with RP cannot be overemphasized.


Assuntos
Demência/diagnóstico , Meningoencefalite/diagnóstico , Policondrite Recidivante/diagnóstico , Demência/etiologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Meningoencefalite/etiologia , Pessoa de Meia-Idade , Policondrite Recidivante/complicações , Tomografia Computadorizada de Emissão de Fóton Único
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