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      Alpha-1-antitrypsin (AAT) deposits in gall bladder adenocarcinoma and liver in partial AAT deficiency (Pi SZ phenotype).

      American journal of clinical pathology
      Adenocarcinoma, analysis, pathology, Aged, Gallbladder Neoplasms, Humans, Liver, Male, Phenotype, alpha 1-Antitrypsin, alpha 1-Antitrypsin Deficiency

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          Abstract

          Alpha-1-antitrypsin (AAT) immunoreactive inclusions were found in an adenocarcinoma of a gall bladder of a patient with Pi SZ phenotype who also had globular AAT accumulation in the liver. The inclusions did not react with antibodies against other plasma proteins, thus suggesting a primary synthesis of AAT in these cells. The presence of AAT in the tumor cells may represent resurgence of an oncofetal antigen, or, indirectly, may mean that AAT-containing cells normally exist in the human non-neoplastic gall bladder. The accumulation of AAT in tumor cells might be a basic process in malignant transformation.

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          Author and article information

          Journal
          6983292
          10.1093/ajcp/78.6.878

          Chemistry
          Adenocarcinoma,analysis,pathology,Aged,Gallbladder Neoplasms,Humans,Liver,Male,Phenotype,alpha 1-Antitrypsin,alpha 1-Antitrypsin Deficiency

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