RESUMO
Patients with vitamin B12 deficiency have protean neurological manifestations that are often insidious. Acute onset of cerebellar dysfunction and extrapyramidal manifestations like dystonia and chorea are rather uncommon in adults. We describe a patient who manifested with acute onset of language dysfunction, chorea and ataxia. There was no history of hypertension, diabetes or ischemic heart disease. He had low serum vitamin B12 and elevated serum homocystine levels. He improved dramatically following B12 replacement therapy. Our patient provides insight into the pathophysiological mechanism of this rare manifestation. Further the importance of considering vitamin B12 deficiency, in country like India, where vegetarian food practice is quite common, is being emphasized.
Assuntos
Isquemia Encefálica/complicações , Ataxia Cerebelar/complicações , Coreia/complicações , Hiper-Homocisteinemia/complicações , Deficiência de Vitamina B 12/sangue , Deficiência de Vitamina B 12/complicações , Adulto , Isquemia Encefálica/etiologia , Isquemia Encefálica/patologia , Ataxia Cerebelar/etiologia , Coreia/etiologia , Coreia/patologia , Humanos , Hiper-Homocisteinemia/patologia , Imageamento por Ressonância Magnética , Masculino , Deficiência de Vitamina B 12/patologiaRESUMO
Central to the diagnosis of Waldenstrom's Macroglobulinemia is the demonstration of bone marrow infiltration by lymphoplasmacytic lymphoma with Ig M monoclonal gammopathy. We describe a patient who presented with a clinical and haematological picture, highly suggestive of Waldenstrom's Macroglobulinemia, but whose serum monoclonal immunoglobulin belonged to Ig A class. Ig A secreting lymphoplasmacytic lymphoma undoubtedly exist but are exceedingly uncommon and their relationship to Waldenstrom's Macroglobulinemia needs to be clarified.