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1.
Orv Hetil ; 155(1): 30-3, 2014 Jan 05.
Artículo en Húngaro | MEDLINE | ID: mdl-24379094

RESUMEN

Wernicke encephalopathy (or Wernicke-Korsakoff encephalopathy) is a rarely diagnosed neurological disorder, which is caused by vitamin B1 deficiency. In the classical form it is characterized by a typical triad (confusion, oculomotor disturbance and ataxia), however, in the majority of the cases only confusion is present. It can be frequently observed in subjects with chronic alcohol consumption, but it may accompany different pathological states of which end stage malignant diseases are the most importants, where confusion may have different backgrounds. The authors present the case of an old male patient with advanced gastric cancer recognised and treated vitamin B1 deficiency, and they draw attention to difficulties of the diagnosis of Wernicke's disease.


Asunto(s)
Linitis Plástica/complicaciones , Linitis Plástica/diagnóstico , Neoplasias Gástricas/complicaciones , Neoplasias Gástricas/diagnóstico , Deficiencia de Vitamina B/complicaciones , Encefalopatía de Wernicke/diagnóstico , Anciano , Diagnóstico Diferencial , Resultado Fatal , Humanos , Masculino , Tiamina/administración & dosificación , Complejo Vitamínico B/administración & dosificación , Deficiencia de Vitamina B/tratamiento farmacológico , Encefalopatía de Wernicke/etiología , Encefalopatía de Wernicke/patología
2.
Orv Hetil ; 154(2): 69-73, 2013 Jan 13.
Artículo en Húngaro | MEDLINE | ID: mdl-23291205

RESUMEN

Insul(in)oma is a usually solitary or, in some cases, multifocal tumor of pancreatic beta cells. It may be a component of multiple endocrine neoplasia type 1. or von Hippel-Lindau syndrome. In typical forms the diagnosis - based on the Whipple triad - is simple, however, it may be difficult to recognize in cases with near normal or only slightly elevated serum insulin levels, as well as in patients with known convulsive episodes. With the case presentation of an 81-year-old woman the authors draw attention to the pitfalls of the correct diagnosis. A special feature of the presented case is that convulsions persisted after surgical removal of the pancreatic neuroendocrine tumor verified with functional and imaging methods. Recurrent or residual tumor was not found, and morphological damage of the brain was absent. In the background of the continuing convulsions cerebrovascular alterations as well as the cytotoxic effect of the hypoglycemia-induced excessive glutamate production can be postulated.


Asunto(s)
Glucemia/metabolismo , Insulina/sangre , Insulinoma/complicaciones , Insulinoma/diagnóstico , Pancreatectomía , Neoplasias Pancreáticas/complicaciones , Neoplasias Pancreáticas/diagnóstico , Anciano de 80 o más Años , Diagnóstico Diferencial , Femenino , Humanos , Insulinoma/sangre , Insulinoma/patología , Insulinoma/cirugía , Neoplasias Pancreáticas/sangre , Neoplasias Pancreáticas/patología , Neoplasias Pancreáticas/cirugía , Convulsiones/etiología , Inconsciencia/etiología
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