Zhang Sheng, Wang Mi, Xue Yi-Hui, Chen Yu-Peng
Department of Pathology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, Fujian Province, China.
World J Gastroenterol. 2007 Nov 21;13(43):5787-93. doi: 10.3748/wjg.v13.i43.5787.
We first report a rare case of metastasis from gastric hepatoid adenocarcinoma (HAC) to cerebral parenchyma, in a 50-year-old Chinese patient. He complained of a one-month history of a paroxysm of headache in the left temple and pars parietalis accompanied with binocular caligation caligo, insensible feeling of limbs and transient anepia. Magnetic resonance (MR) imaging revealed a spherical occupying lesion in the left posterior-temple lobe which was clinically diagnosed as a metastatic tumor. Three years ago, the patient accepted total gastrectomy as he was pathologically diagnosed at gastroscopy having an adenocarcinoma. Eight months after gastrectomy, the occupying lesion in liver was detected by ultrasound and CT, and he accepted transcatheter arterial embolization. Before operation of the brain metastasis, no obvious abnormality was found in liver by ultrasound. Histopathological characteristics of the brain tumor were identical to those of stomach tumor. The growth pattern of both tumors showed solid cell nests. The tumor cells were polygonal, and had abundant eosinophilic cytoplasm and round nuclei with obvious nucleoli. Sinusoid-like blood spaces were located between nodular tumor cells. Immunohistochemistry-stained tumor cells were positive for AFP and negative for Hep-Par-1. According to these histopathological findings, both tumors were diagnosed as HAC and metastatic HAC. The patient remained alive 16 mo after tumorectomy of the cerebral metastasis. The differential diagnosis of brain metastasis from metastatic tumors should use a panel of antibodies to avoid confusing with the brain metastasis of hepatocellular carcinoma (HCC). This paper describes this rare case of metastasis from gastric hepatoid adenocarcinoma to cerebral parenchyma, and provides a review of the literature concerning its histopathological and immunohistochemical characteristics.
我们首次报告了一例50岁中国患者胃肝样腺癌(HAC)转移至脑实质的罕见病例。他主诉左侧颞部和顶叶阵发性头痛1个月,伴有双眼视力模糊、肢体麻木感和短暂性失语。磁共振成像(MR)显示左侧颞叶后部有一个球形占位性病变,临床诊断为转移性肿瘤。三年前,患者因胃镜病理诊断为腺癌接受了全胃切除术。胃切除术后8个月,超声和CT检查发现肝脏有占位性病变,随后接受了经导管动脉栓塞术。在脑转移瘤手术前,超声检查肝脏未发现明显异常。脑肿瘤的组织病理学特征与胃肿瘤相同。两种肿瘤的生长模式均显示为实性细胞巢。肿瘤细胞呈多边形,胞质嗜酸性丰富,核圆形,核仁明显。结节状肿瘤细胞之间可见窦状血腔。免疫组化染色肿瘤细胞AFP阳性,Hep-Par-1阴性。根据这些组织病理学结果,两种肿瘤均诊断为HAC和转移性HAC。脑转移瘤切除术后16个月患者仍存活。转移性肿瘤脑转移的鉴别诊断应使用一组抗体,以避免与肝细胞癌(HCC)脑转移混淆。本文描述了这例胃肝样腺癌转移至脑实质的罕见病例,并对其组织病理学和免疫组化特征的相关文献进行了综述。