Takahashi Toshihide, Ishikawa Eiichi, Masuda Yosuke, Yamamoto Tetsuya, Sato Taiki, Shibuya Makoto, Matsumura Akira
Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, 305-8575, Japan.
Case Rep Surg. 2012;2012:473790. doi: 10.1155/2012/473790. Epub 2012 Dec 24.
Intracranial nongerminomatous germ cell tumors (NGGCTs) in unusual locations are extremely rare. Here, we report a case of a yolk sac tumor in the frontal lobe in a middle-aged patient. A 42-year-old man was admitted to our hospital for headache and nausea. Magnetic resonance imaging (MRI) showed an enhanced mass lesion with a marked cyst component. The serum alpha-fetoprotein (αFP) level was extremely high. Histological examination of specimens after subtotal removal revealed a primary mixed germ cell tumor with extensive yolk sac tumor elements, often referred to as an intracranial "yolk sac tumor." The preoperative diagnosis of NGGCTs in unusual age and locations is extremely difficult. Clinicians should consider the possibility of NGGCTs, including yolk sac tumors, when intracranial tumors with unusual MRI findings are encountered.
颅内非生殖细胞瘤性生殖细胞肿瘤(NGGCTs)发生于不寻常部位极为罕见。在此,我们报告一例中年患者额叶卵黄囊瘤病例。一名42岁男性因头痛和恶心入院。磁共振成像(MRI)显示一个强化肿块病变,伴有明显的囊肿成分。血清甲胎蛋白(αFP)水平极高。次全切除术后标本的组织学检查显示为原发性混合性生殖细胞肿瘤,伴有广泛的卵黄囊瘤成分,常被称为颅内“卵黄囊瘤”。在不寻常年龄和部位对NGGCTs进行术前诊断极为困难。当遇到具有不寻常MRI表现的颅内肿瘤时,临床医生应考虑NGGCTs的可能性,包括卵黄囊瘤。