Hepatocellular carcinoma in patients with thalassaemia syndromes: clinical characteristics and outcome in a long term single centre experience

Saved in:
Bibliographic Details
Published inBritish journal of haematology Vol. 150; no. 2; pp. 245 - 247
Main Authors Restivo Pantalone, Gaetano, Renda, Disma, Valenza, Franco, D’Amato, Fabio, Vitrano, Angela, Cassarà, Filippo, Rigano, Paolo, Salvo, Veronica Di, Giangreco, Antonino, Bevacqua, Elvira, Maggio, Aurelio
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.07.2010
Blackwell
Subjects
Adult
Aged
Anemias. Hemoglobinopathies
Biological and medical sciences
Carcinoma, Hepatocellular - etiology
cirrhosis
Diseases of red blood cells
Female
Gastroenterology. Liver. Pancreas. Abdomen
Hematologic and hematopoietic diseases
hepatitis C
Hepatitis C, Chronic - complications
hepatocellular carcinoma
Humans
iron overload
Iron Overload - complications
Liver Neoplasms - etiology
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Metabolic diseases
Metals (hemochromatosis...)
Middle Aged
Other diseases. Semiology
Other metabolic disorders
Prognosis
thalassaemia
Thalassemia - therapy
Transfusion Reaction
Tumors
Human
Iron overload
Hemoglobinopathy
Prognosis
Hematology
hepatitis C
Metabolic diseases
Hepatic disease
Hepatocellular carcinoma
Thalassemia
Hemopathy
Iron
Malignant tumor
Long term
Genetic disease
Infection
Liver cancer
Cirrhosis
Hemolytic anemia
Viral disease
Digestive diseases
thalassaemi
Cancer
Viral hepatitis C
Online AccessGet full text

Cover

More Information
Bibliography:The same day this report was submitted, on November 25th 2009, another patient received orthotopic liver transplantation and survived her treatment (patient n.1, a 54 years old woman with thalassaemia major).
SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:0007-1048
1365-2141
DOI:10.1111/j.1365-2141.2010.08180.x