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Recurrent Vertebrobasilar Strokes Associated With Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE).
Collía Fernández, Alejandra; García Sánchez, Juan M; Rivera-Pérez de Rada, Pablo; Fernández-Avellaneda, Pedro; Rodrigo Armenteros, Patricia; Torre Salaberri, Ignacio; Castillo Calvo, Beatriz; Gómez Muga, Juan J; Gil Alzueta, María D C; García-Moncó, Juan C.
Afiliación
  • Collía Fernández A; Departments of Neurology.
  • García Sánchez JM; Departments of Neurology.
  • Rivera-Pérez de Rada P; Ophthalmology.
  • Fernández-Avellaneda P; Ophthalmology.
  • Rodrigo Armenteros P; Departments of Neurology.
  • Torre Salaberri I; Rheumatology.
  • Castillo Calvo B; Departments of Neurology.
  • Gómez Muga JJ; Radiology, Osakidetza Basque Health Service, Basurto University Hospital, Bilbao, Spain.
  • Gil Alzueta MDC; Departments of Neurology.
  • García-Moncó JC; Departments of Neurology.
Neurologist ; 25(5): 131-136, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32925484
INTRODUCTION: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an ophthalmologic condition of likely immune origin. Typically, it presents as a chorioretinitis with bilateral visual disturbance and characteristic funduscopic lesions of the retinal pigment epithelium. APMPPE has been associated with several systemic and neurological complications, including cerebrovascular diseases. CASE REPORT: A 58-year-old woman presented with sudden right hemiparesis and dysarthria, with magnetic resonance imaging evidence of an acute ischemic lesion in the left pons. Five days later, she developed contralateral hemiparesis and evolved into a locked-in syndrome. A new lesion located at the right pontomedullary junction was detected by magnetic resonance imaging. The patient developed a visual deterioration that had started 1 week before admission. An ophthalmologic evaluation showed visual acuity loss (20/200 in both eyes) and characteristic yellow-white lesions in the posterior pole of both eyes. Laboratory analyses were remarkable for positive antinuclear antibodies, an elevated erythrocyte sedimentation rate, and C-reactive protein. The cerebrospinal fluid showed elevated protein levels, lymphocytic pleocytosis, and normal glucose levels. The fundoscopy findings together with recurrent strokes led to the diagnosis of APMPPE and appropriate immunomodulatory treatment with corticosteroids and azathioprine was started. CONCLUSIONS: This case illustrates the importance of careful evaluation and high clinical suspicion for this entity when dealing with patients with new-onset headache or stroke associated with visual impairment. Proper ophthalmologic evaluation is important so that adequate therapy is established.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes de Puntos Blancos Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Neurologist Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes de Puntos Blancos Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Neurologist Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos