Title | Multifocal hepatocellular carcinoma and precancerous lesions in a patient with autoimmune hepatitis-related cirrhosis. |
Publication Type | Journal Article |
Year of Publication | 2008 |
Authors | Ward SC, Deniz K, Roayaie S, Qin L |
Journal | Semin Liver Dis |
Volume | 28 |
Issue | 1 |
Pagination | 123-7 |
Date Published | 2008 Feb |
ISSN | 0272-8087 |
Keywords | Adult, Biopsy, Needle, Carcinoma, Hepatocellular, Diagnosis, Differential, Female, Follow-Up Studies, Hepatitis, Autoimmune, Humans, Liver Cirrhosis, Liver Neoplasms, Liver Transplantation, Magnetic Resonance Imaging, Precancerous Conditions |
Abstract | A 44-year-old woman with a 29-year history of autoimmune hepatitis (AIH) received a living donor liver transplant for multifocal hepatocellular carcinoma (HCC) and cirrhosis in 2007. Her initial laboratory workup at our institution in 1996 revealed a positive antismooth muscle antibody with a titer of 1:640. Serum electrophoresis showed a monoclonal gamma globulin spike with elevated IgG, IgA, and IgM. The patient was negative for hepatitis B and hepatitis C (HCV) by serology and serum polymerase chain reaction. She was treated with corticosteroids and azathioprine, but her disease progressed. In 1997, a liver needle biopsy revealed cirrhosis and a focus of small cell change. In 2004, a 2-cm exophytic mass was detected on magnetic resonance imaging. Follow-up imaging in 2005 and 2006 showed growth of the exophytic mass and development of new tumors. The exophytic mass was treated with ethanol ablation and she received a transplant. Examination of the explant revealed multiple high-grade dysplastic nodules and four moderately differentiated HCCs, one of which is arising in a high-grade dysplastic nodule. We believe this to be the first case in the English literature documenting the presence of preneoplastic lesions in an HCV-negative patient with AIH who developed HCC. |
DOI | 10.1055/s-2008-1040326 |
Alternate Journal | Semin Liver Dis |
PubMed ID | 18293282 |
Related Faculty:
Lihui Qin, M.D., Ph.D.