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Медицинская библиотека · Revista de neurologia · 2006

[Unusual cortical compromise in a case of Wernicke's encephalopathy].

Blanco-Múñez O, Suárez-Gauthier A, Martín-García H, Díaz-Konrad V, San Antonio-Román V, Cabello A

Клинический случайАннотация на английскомСтатьяПеревод пока не подготовлен

Аннотация

INTRODUCTION

Wernicke's encephalopathy (WE) is a metabolic disease due to thiamine deficiency; only 10% of cases are diagnosed pre-mortem. Symptoms of WE include ophthalmoplegia, nistagmus, ataxia and mental confusion; post-mortem examination shows characteristic symmetrical lesions in the mamillary bodies (MB), hypothalamus, thalamus, brain stem and cerebellum with spongiosis, demyelination, vascular proliferation and relative preservation of neurons.

CASE REPORT: 50 years-old male with alcoholic hepatopathy and orthotopic hepatic transplant who suffered a second surgical intervention 10 days after due to problems in the biliar anastomosis. After this second surgery he showed an altered mental status, with fluctuating global confusion, disorientation and agitation. He died 52 days after the hepatic transplantation. Autopsy study showed bilateral broncopneumonia, brown discoloration of the MB and bilateral linear lesions in the cortex of both motor gyri, which histologically showed identical to the MB lesions with demyelination, capillary and glial proliferation and preservation of neurons. Alzheimer type II astrocytes were also found in basal nuclei and cortex.

CONCLUSIONS

Typical WE lesions affect MB, hypothalamus, thalamus, brain stem and cerebellum; cortical lesions, when found, are due to hepatocerebral degeneration with Alzheimer type II astrocytes or to the citopathic effects of ethanol. In our case, cortical lesions were identical to the lesions found in MB, an extraordinary finding which we have not found reported in the literature.

Для цитирования: Blanco-Múñez O, Suárez-Gauthier A, Martín-García H, Díaz-Konrad V, San Antonio-Román V, Cabello A. [Unusual cortical compromise in a case of Wernicke's encephalopathy].. Revista de neurologia. 2006.

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