High risk of primary liver cancer in a cohort of 179 patients with Acute Hepatic Porphyria. Issue 6 (23rd January 2013)

• Record Type: Journal Article
• Authors: Sardh, Eliane; Wahlin, Staffan; Björnstedt, Mikael; Harper, Pauline; Andersson, Dan E. H.
• Is Part Of: Journal of inherited metabolic disease. Volume 36:Issue 6(2013)
• Page Start: 1063
• Page End: 1071
• Publication Date: 2013-01-23
• Subjects: Metabolism, Inborn errors of -- Periodicals; Metabolism -- Disorders -- Periodicals; 616.39042
• DOI: 10.1007/s10545-012-9576-9
• Languages: English
• ISSNs: 0141-8955

Abstract

Abstract: Background/aims: Previous studies have indicated a high risk of hepatocellular carcinoma in acute hepatic porphyrias. In this retrospective study we present the incidence of primary liver cancer and clinical characteristics in a cohort of 179 acute porphyria patients above the age of 50 years. Methods: Twenty‐three cases with primary liver cancer were found either by a surveillance program or due to clinical suspicion. Standardized rate ratio was used to estimate the relative risk of primary liver cancer after indirect standardization. Survival data were calculated using the Kaplan‐Meier method. Results: The mean age at diagnosis was 69 years. Hepatocellular carcinoma was found in 19 patients while four patients had cholangiocarcinoma or a combination of the two. Four patients had underlying cirrhosis. Mean tumour size was 4.3 cm in the surveillance group and 10.3 cm in the non‐surveillance group ( p = 0.01). The overall relative risk of primary liver cancer was 86 above the age of 50: 150 for women and 37 for men. Mean survival time was 5.7 years. Conclusion: Acute hepatic porphyria carries a high risk of primary liver cancer above the age of 50 which warrants ultrasound surveillance. Sex distribution and frequency of cirrhosis differs from more common aetiologies of primary liver cancer.