| Literature DB >> 19207587 |
Toshiro Masuda1, Toru Beppu, Kei Horino, Hiroyuki Komori, Hiromitsu Hayashi, Hirohisa Okabe, Ryuu Ootao, Hasita Horlad, Yoshifumi Baba, Shiho Miyase, Hiroshi Takamori, Hideo Baba.
Abstract
Hepatoblastoma is a rare malignancy in adults. It is often diagnosed after the appearance of symptoms, therefore, the tumor size tends to be larger. In patients with no indication for a hepatic resection, the prognosis of adult hepatoblastoma is quite poor. A 54-year-old man with hepatitis C virus-associated liver cirrhosis was initially treated with a hepatic resection for a hepatic tumor, 3 cm in diameter. The tumor consisted of osteoid-like and cartilaginous foci, myxomatous stroma, and poorly differentiated hepatocellular carcinomatous cells and was diagnosed as a mixed epithelial and mesenchymal hepatoblastoma. Two years after the first operation, multicentric hepatocellular carcinomas developed in the remnant liver and were successfully treated with a secondary hepatic resection combined with radio-frequency ablation. The patient is now alive with no recurrence at 5 years after the initial hepatectomy. To the best of our knowledge, the primary hepatoblastoma was the smallest such tumor reported and this is the first report of a metachronous hepatoblastoma and hepatocellular carcinoma in an adult hepatitis patient.Entities:
Year: 2009 PMID: 19207587 DOI: 10.1111/j.1872-034X.2008.00471.x
Source DB: PubMed Journal: Hepatol Res ISSN: 1386-6346 Impact factor: 4.288