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Case Report
BRAIN

Proton MR Spectroscopy in Wernicke Encephalopathy

Carlos A. Rugiloa,c, Marcela C. Uribe Rocad, Maria C. Zurrua, Arístides A. Capizzanoc, Gustavo A. Pontellob and Emilia M. Gattoa,d

a the Servicio de Neurología, Buenos Aires
b Sanatorio Mitre, the Servicio de Clínica Médica, Buenos Aires
c Fundación Femien, Buenos Aires
d the Programa de Parkinson y Movimientos Anormales, Hospital de Clínicas, Buenos Aires, Argentina

Address reprint requests to Emilia Mabel Gatto, MD, Juramento 1155, 3° A, Buenos Aires, Argentina, C1428DMK

Summary: Wernicke encephalopathy is caused by thiamine deficiency. Although the clinical picture has been well established for some time, clinical diagnosis is attained in only 20% of the cases. MR imaging techniques contribute to early diagnosis of Wernicke encephalopathy. We herein report MR imaging and proton MR spectroscopic findings for a patient with clinical and biochemical features consistent with Wernicke encephalopathy. Increased lactate and typical MR imaging findings are discussed in the context of the known pathophysiology of Wernicke encephalopathy.




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