Yokoi Kentaro, Akiyama Masaharu, Yanagisawa Takaaki, Yoshino Masami, Nakazaki Hiromichi, Takahashi Koichi, Takahashi-Fujigasaki Junko, Kanetsuna Yukiko, Yamada Hisashi, Oi Shizuo, Eto Yoshikatsu
Department of Pediatrics, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Pediatr Blood Cancer. 2005 May;44(5):516-20. doi: 10.1002/pbc.20274.
Congenital intracranial tumors are extremely rare and account only for 0.5%-1.5% of brain tumors in children. We report a large intrauterine congenital teratoma in a female fetus at gestation weeks 37, which was diagnosed by detecting the tumor and associated craniomegaly with ultrasonography (US) and magnetic resonance (MR) imaging. The tumor had replaced the cerebral hemispheres and produced prenatal manifestations. Pathologic examination showed an immature teratoma, which was differentiated from all three germ layers. Microarray analysis revealed upregulation of ten genes and downregulation of three genes, as well as upregulation of 41 genes of ribosomal proteins in teratoma cells, compared to normal brain tissue of the patient. The data from the microarray analysis offer not only the potential to help define disease pathogenesis but may also provide clues to identify potential molecular therapeutic targets.
先天性颅内肿瘤极为罕见,仅占儿童脑肿瘤的0.5%-1.5%。我们报告了一例孕37周女性胎儿的巨大宫内先天性畸胎瘤,通过超声(US)和磁共振(MR)成像检测肿瘤及相关的巨头畸形而得以诊断。该肿瘤取代了大脑半球并产生了产前表现。病理检查显示为未成熟畸胎瘤,由所有三个胚层分化而来。与患者正常脑组织相比,基因芯片分析显示畸胎瘤细胞中有10个基因上调、3个基因下调,以及41个核糖体蛋白基因上调。基因芯片分析的数据不仅有助于明确疾病发病机制,还可能为识别潜在的分子治疗靶点提供线索。