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Review
. 2010 May;138(5):581-5.
Epub 2010 Jul 12.

[Porphyria cutanea tarda, hemosiderosis and hepatocellular carcinoma: report of one case]

[Article in Spanish]
Affiliations
  • PMID: 20668813
Free article
Review

[Porphyria cutanea tarda, hemosiderosis and hepatocellular carcinoma: report of one case]

[Article in Spanish]
Carolina Whittle et al. Rev Med Chil. 2010 May.
Free article

Abstract

Porphyria cutanea tarda (PCT) is a hereditary or acquired disease. It can be unleashed by iron overload, alcohol, estrogens and other conditions. In these patients, hepatic involvement can be associated to cirrhosis, iron overload or C and B viral infections, that are predisposing factors for hepatocellular carcinoma. We report a 69-year-old man with PTC, hemosiderosis and hepatocarcinoma. The tumor was diagnosed during a routine ultrasound examination for early detection of malignant lesions. The patient was subjected to a right hepatic excision. The pathological examination of the surgical piece confirmed the diagnosis and disclosed free surgical margins. After 18 months of follow up, the patient had a relapse and a liver transplantation was performed.

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