我们遇见自然病程长达近8年的罕见患者1例。现摘要报告如下:林某,女,50岁,福建闽候人,汉族,工人。于1976年6月7日肿瘤普查检测,AFP血凝法为1∶10(4++),1∶100(+++)。11天后复查为1∶10(+)1∶100(++),1∶1000(+++);AFP定性对流法和扩散法均阳性。同年7月13日和28日二次放射性核素肝扫描示肝右叶下方占位性病变。AFP定量高达150,000ng/ml。此后多年患者无明显不适,未作特殊诊治。1983年9月初因修房搬移家具,突发腹内大出血。紧急剖腹探查发现左肝门处有一5×6×6cm大的 We met one rare patient who had a natural course for nearly 8 years. The summary report is as follows: Lin Mou, female, 50 years old, Fujian Clerk, Han nationality, worker. On June 7, 1976, the tumor census test showed that the AFP hemagglutination method was 1:10 (4++) and 1:100 (+++). After 11 days, the review was 1:10 (+) 1:100 (++), 1:1000 (+++); AFP was qualitatively positive by both convection and diffusion methods. On the 13th and 28th of the same year, secondary radionuclide liver scans showed lesions occupying the right lower lobe. AFP quantified up to 150,000 ng/ml. After many years, the patient did not have obvious discomfort and did not undergo special treatment. In early September 1983, due to move the furniture repair room, sudden intra-abdominal bleeding. Emergency exploratory laparotomy revealed a 5×6×6 cm large left hepatic portal