Development of hepatocellular carcinoma following treatment with6-mercaptopurine for ulcerative colitis: investigation of chromosomal aberration by comparative genomic hybridization |
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Authors: | Kentaro Nakao Akira Tsunoda Yoshinori Shimizu Koji Takenaka Koji Morohara Naoto Suzuki Katsuo Yamazaki Takeshi Aoki Mitsunori Hoshino Mitsuo Kusano Eri Kitadai Toshikazu Kurihara Yoshiaki Takeuchi Michio Imawari |
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Affiliation: | (1) Second Department of Surgery, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 146-8666, Japan;(2) Link Genomics Co., Tokyo, Japan;(3) Second Department of Internal Medicine, Showa University School of Medicine, Tokyo, Japan |
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Abstract: | In a 64-year-old man who had been treated with prednisolone (PSL) and 6-mercaptopurine (6MP) for a long period, for ulcerative colitis (UC), hepatocellular carcinoma (HCC) was detected incidentally. The UC was in remission with these medications. After he had been taking these medications for about 8 years, HCC was detected by computed tomography (CT), done for the evaluation of an other disease. Blood chemistry examination results were normal, except that the protein induced by vitamin K antagonist (PIVKA)-II level was 7940 AU/ml. We performed resection of liver segment V. With comparative genomic hybridization, chromosomal aberrations were recognized; these were gains of 1q, 3ptel-21, 8p12, and 22q11.23–22q13.1. Generally, HCC is associated with hepatitis virus infection in most cases, but in this patient, the HCC was not related to hepatitis C virus (HCV) or HBV. It is presumed that this case was related to the immunosuppressive therapy for UC and was associated with the gains of 1q, 3p, and 8p. |
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Keywords: | Hepatocellular carcinoma 6-Mercaptopurine Ulcerative colitis Comparative genomic hybridization (CGH) |
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