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J Clin Gastroenterol ; 4(3): 269-73, 1982 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-6980239

RESUMO

We report a 73-year-old woman with homozygous ZZ alpha-1-antitrypsin deficiency (AATD), micronodular cirrhosis, cholestatic jaundice, and emphysema. An elevated SGOT/SGPT ratio was noted in the absence of chronic alcoholism. ERCP demonstrated a normal extrahepatic biliary system and suggested obstruction of the intrahepatic ducts. An operative liver biopsy demonstrated periodic acid-Schiff-positive, diastase resistant intracytoplasmic inclusion bodies. This patient reminds us that metabolic causes of cryptogenic liver disease need to be considered, even in the elderly. We review briefly the literature concerning AATD and liver disease.


Assuntos
Cirrose Hepática/etiologia , Deficiência de alfa 1-Antitripsina , Idoso , Alelos , Feminino , Humanos , Fígado/patologia , Testes de Função Hepática , Fenótipo , alfa 1-Antitripsina/genética
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