TY - JOUR
T1 - Hepatocellular carcinoma occurring in hepatobiliary fibropolycystic disease
AU - Kinugasa, Hideaki
AU - Nouso, Kazuhiro
AU - Kobayashi, Yoshiyuki
AU - Yasunaka, Tetsuya
AU - Onishi, Hideki
AU - Nakamura, Shinichiro
AU - Shiraha, Hidenori
AU - Takayama, Hiroki
AU - Toshimori, Junichi
AU - Kuwaki, Kenji
AU - Hagihara, Hiroaki
AU - Miyake, Yasuhiro
AU - Ikeda, Fusao
AU - Takaki, Akinobu
AU - Kobashi, Haruhiko
AU - Yamamoto, Kazuhide
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2011/3
Y1 - 2011/3
N2 - Congenital hepatic fibrosis (CHF) and bile duct hamartomas (von Meyenburg complexes) are hepatobiliary fibropolycystic diseases. There have been several reports of liver neoplasias arising in hepatobiliary fibropolycystic diseases. However, most of them were cholangiocarcinomas and cases involving hepatocellular carcinoma (HCC) are rare. A 51-year-old woman was found to have multiple hepatic tumors by ultrasonography and enhanced computed tomography (CT) during a regular work-up for the recurrence of lung cancer and thyroid cancer, which had been surgically removed 4 and 3years ago, respectively. Nodules were observed at S3, S5, and S6 (2cm in diameter). All of the nodules were hyperattenuated at the early arterial phase, and the main tumor at S5 showed hypoattenuation at the delayed phase on dynamic CT and magnetic resonance imaging (MRI). HCC was suspected from these findings. She also suffered from multiple small cystic lesions in the liver. The surgically removed liver showed HCC arising in CHF, which is a rare histological finding.
AB - Congenital hepatic fibrosis (CHF) and bile duct hamartomas (von Meyenburg complexes) are hepatobiliary fibropolycystic diseases. There have been several reports of liver neoplasias arising in hepatobiliary fibropolycystic diseases. However, most of them were cholangiocarcinomas and cases involving hepatocellular carcinoma (HCC) are rare. A 51-year-old woman was found to have multiple hepatic tumors by ultrasonography and enhanced computed tomography (CT) during a regular work-up for the recurrence of lung cancer and thyroid cancer, which had been surgically removed 4 and 3years ago, respectively. Nodules were observed at S3, S5, and S6 (2cm in diameter). All of the nodules were hyperattenuated at the early arterial phase, and the main tumor at S5 showed hypoattenuation at the delayed phase on dynamic CT and magnetic resonance imaging (MRI). HCC was suspected from these findings. She also suffered from multiple small cystic lesions in the liver. The surgically removed liver showed HCC arising in CHF, which is a rare histological finding.
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U2 - 10.1111/j.1872-034X.2010.00761.x
DO - 10.1111/j.1872-034X.2010.00761.x
M3 - Article
C2 - 21338456
AN - SCOPUS:79951807578
SN - 1386-6346
VL - 41
SP - 277
EP - 281
JO - Hepatology Research
JF - Hepatology Research
IS - 3
ER -