Department of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Hepatol Res. 2009 May;39(5):525-30. doi: 10.1111/j.1872-034X.2008.00471.x. Epub 2009 Jan 12.
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.
肝母细胞瘤在成人中较为罕见。它通常在出现症状后被诊断出来,因此肿瘤的大小往往更大。对于没有肝切除术指征的患者,成人肝母细胞瘤的预后相当差。一名 54 岁男性,患有丙型肝炎病毒相关的肝硬化,最初因肝肿瘤接受了肝切除术治疗,肿瘤直径为 3 厘米。肿瘤由骨样和软骨样灶、黏液样基质和低分化肝细胞癌组成,被诊断为混合上皮和间叶性肝母细胞瘤。第一次手术后两年,残余肝脏中出现多中心肝细胞癌,并成功接受了二次肝切除术联合射频消融治疗。患者在初次肝切除术后 5 年无复发,目前仍存活。据我们所知,这是报告的最小的原发性肝母细胞瘤,也是首例成人肝炎患者的肝母细胞瘤和肝细胞癌的同时性发生。