A clinical review of congenital hepatic fibrosis diagnosed in adulthood: presentation, complications, and outcomes

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Summary: Congenital hepatic fibrosis (CHF) is a hereditary disease that may require liver and kidney transplantation. Patients undergoing liver transplantation for CHF have good short-term and long-term survival rates, with no significant differences in outcomes between simultaneous liver-kidney and isolated liver transplantation. Half of patients with CHF also require kidney transplantation.

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Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease

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Article Gastroenterology & Hepatology

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease

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A clinical review of congenital hepatic fibrosis diagnosed in adulthood: presentation, complications, and outcomes

Related references

Baveno VII - Renewing consensus in portal hypertension

Liver transplantation for congenital hepatic fibrosis

Diagnosis of Congenital Hepatic Fibrosis in Adulthood A Multidisciplinary Approach

Diagnosis, Staging, and Management of Hepatocellular Carcinoma: 2018 Practice Guidance by the American Association for the Study of Liver Diseases

Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease

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