Takayasu K, Itabashi M, Moriyama N
Department of Diagnostic Radiology, National Cancer Center Hospital, Tokyo, Japan.
Clin Radiol. 1994 Aug;49(8):579-81. doi: 10.1016/s0009-9260(05)82944-7.
A 57-year-old man with high alpha-fetoprotein (AFP) and suspected submucosal tumour of the stomach was referred for investigation. A 6 cm hypervascular tumour with tumour vessels in the left diaphragm was diagnosed by a combination of angiography and computed tomography. At laparotomy, the tumour was confirmed to be located just beneath the left diaphragm and to be isolated from the liver parenchyma. The resected specimen was histopathologically hepatocellular carcinoma. The level of AFP returned to normal, and the patient is free of recurrence 8 years after operation.
一名57岁男性,甲胎蛋白(AFP)水平高,怀疑有胃黏膜下肿瘤,前来接受检查。通过血管造影和计算机断层扫描相结合的方法,诊断出左膈有一个6厘米的高血管肿瘤,伴有肿瘤血管。剖腹手术时,证实肿瘤位于左膈下方,与肝实质分离。切除的标本经组织病理学检查为肝细胞癌。AFP水平恢复正常,患者术后8年无复发。