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Liver Transplantation to Treat Suspected Hepatocellular Carcinoma in Iron-Free Foci in Congenital Hemochromatosis: Case Report

M Quante, C Benckert, A Thelen, D Uhlmann… - Transplantation …, 2011 - Elsevier
... The current literature reports approximately 30 patients with HCC in congenital hemochromatosis
in the absence of cirrhosis. ... [8] and [9]. Hepatocellular carcinoma in congenital hemochromatosis
is different from HCC in livers with cirrhosis due to other underlying diseases. ...
Related articles - All 2 versions

[HTML] Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: a case report

[HTML] from nih.govMR Ghadir, M Bagheri… - Journal of medical case …, 2011 - ncbi.nlm.nih.gov
Congenital hepatic fibrosis is an uncommon cause of portal hypertension. Despite the presence
of portal hypertension, hepatocellular and renal function are usually well preserved. Congenital
hepatic fibrosis is included in the group of congenital diseases of fibropolycystic ...
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Imaging of biliary disorders in children

C Rozel, L Garel, F Rypens, L Viremouneix… - Pediatric radiology, 2011 - Springer
... of the biliary tree. Combined increased production and decreased excretion is seen
in sepsis, infection and congenital cirrhosis. Biliary disorders are often overlooked
in the pediatric age group. Pediatric biliary tract diseases ...
Cited by 2 - Related articles - All 3 versions

[HTML] Situs inversus totalis and secondary biliary cirrhosis: a case report

[HTML] from comparative-hepatology.comHM Sökmen, K Özdil, T Çalhan… - Comparative …, 2011 - comparative-hepatology.com
Situs inversus totalis is is a congenital anomaly associated with various visceral
abnormalities, but there is no data about the relationship between secondary biliary
cirrhosis and that condition. We here present a case of a 58 ...
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Congenital Extrahepatic Portosystemic Shunts (Abernethy Malformation): A Histopathologic Evaluation

M Lisovsky, AA Konstas… - The American Journal of …, 2011 - journals.lww.com
... study, the imaging findings of all potential congenital portosystemic shunt cases were reviewed.
Patients whose shunts had radiologic features that suggested that they were acquired shunts
were excluded. Patients were excluded if they had established cirrhosis or imaging ...

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