Takayasu K, Muramatsu Y, Moriyama N, Makuuchi M, Yamazaki S, Kishi K, Yoshino M
Department of Diagnostic Radiology, National Cancer Center Hospital, Tokyo, Japan.
Am J Gastroenterol. 1989 May;84(5):544-7.
Double primary liver cancer, i.e., hepatocellular carcinoma (HCC) and cholangiocellular carcinoma (CCC), was detected by ultrasound (US) during the follow-up of chronic liver disease, and was safely resected in two patients, one synchronously and the other metachronously. On admission, laboratory data were normal except for slightly abnormal liver function tests. One patient (case 1) had a 5.1-cm white firm CCC with several small daughter lesions around it which was enhanced late in computed tomography, and a 2.1-cm well-circumscribed HCC with a pseudocapsule; the two were situated very close to one another in the right posterior segment of the liver. Another patient (case 2) had a small 1.5-cm CCC in the anterior superior area, and 6 yr after the first resection, alpha-fetoprotein gradually increased and a 4-cm HCC was detected anew and resected; the preoperative diagnosis made by US and ethiadol-computed tomography was correct. The histopathological diagnosis of the noncancerous portion was chronic active hepatitis in both cases. However, it changed to precirrhosis in case 2 during the follow-up.
在慢性肝病随访期间,通过超声(US)检测到双原发性肝癌,即肝细胞癌(HCC)和胆管细胞癌(CCC),并对两名患者进行了安全切除,其中一例为同时性,另一例为异时性。入院时,除肝功能检查略有异常外,实验室数据均正常。一名患者(病例1)有一个5.1厘米的白色实性CCC,周围有几个小的子病灶,在计算机断层扫描中晚期强化,还有一个2.1厘米边界清晰、有假包膜的HCC;两者位于肝脏右后段,彼此非常靠近。另一名患者(病例2)在前上区域有一个1.5厘米的小CCC,首次切除6年后,甲胎蛋白逐渐升高,新发现并切除了一个4厘米的HCC;超声和碘海醇计算机断层扫描做出的术前诊断是正确的。两例患者非癌部分的组织病理学诊断均为慢性活动性肝炎。然而,病例2在随访期间转变为肝硬化前期。