Journal of Clinical Medicine (Apr 2023)

Intrahepatic Cholangiocarcinoma and Acute Intermittent Porphyria: A Case Report

  • Claudio Carmine Guida,
  • Maria Nardella,
  • Leonardo Fiorentino,
  • Tiziana Latiano,
  • Francesco Napolitano,
  • Gaetano Ferrara,
  • Annalisa Crisetti,
  • Gianluigi Mazzoccoli,
  • Francesco Aucella,
  • Filippo Aucella

DOI
https://doi.org/10.3390/jcm12093091
Journal volume & issue
Vol. 12, no. 9
p. 3091

Abstract

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Patients suffering from different forms of acute hepatic porphyria present a high risk of primary liver cancer, specifically hepatocellular carcinoma and cholangiocarcinoma, determined by the activity of the disease even though an exact mechanism of carcinogenesis has not been recognized yet. Here, we present the clinical case of a 72-year-old woman who, approximately 29 years after the diagnosis of acute intermittent porphyria, presented with intrahepatic cholangiocarcinoma with a histological diagnosis of adenocarcinoma starting from the biliary-pancreatic ducts, which was diagnosed during the clinical and anatomopathological evaluation of a pathological fracture of the femur.

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