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Bull Soc Pathol Exot ; 108(4): 242-6, 2015 Oct.
Artículo en Francés | MEDLINE | ID: mdl-26168850

RESUMEN

Primitive Gougerot-Sjögren syndrome (PGSS) is a systemic autoimmune exocrinopathy in which twenty percent of affected patients develop neurological manifestations. It has been little described in the Black African literature. We report a case of PGSS in a 64-year-old Black woman as revealed by neurological manifestations in an inflammatory context. Central neuropathy was present and the patient fulfilled at least four of the six Vitali American-European diagnostic criteria. There were abnormal aspects on the sylvian artery and hyperintense lesions of periventricular predominance. PGSS is a serious disease which we must consider when we encounter any unexplained neurological manifestations especially those associated with vasculitic lesions.


Asunto(s)
Encefalopatías/diagnóstico , Síndrome de Sjögren/complicaciones , Síndrome de Sjögren/diagnóstico , Población Negra , Encefalopatías/etiología , Femenino , Humanos , Imagen por Resonancia Magnética , Persona de Mediana Edad , Togo
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