Utsuki Satoshi, Oka Hidehiro, Sagiuchi Takao, Shimizu Satoru, Suzuki Sachio, Fujii Kiyotaka
Department of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
J Neurosurg. 2007 Jun;106(6):1067-9. doi: 10.3171/jns.2007.106.6.1067.
The recurrence of intracranial mature teratomas as germ cell tumors of different histological types is rarely reported. The authors describe the first case of the malignant transformation of an intracranial mature teratoma into a yolk sac tumor in a 16-year-old boy who presented with a 1-month history of anorexia and somnolence. Seven years prior to this presentation, the boy had undergone surgery for extirpation of a mature pineal teratoma. Computed tomography images obtained at his second presentation revealed a homogeneously enhanced mass within the third ventricle. The tumor was resected and the results of a histological examination were consistent with a yolk sac tumor. After resection, the patient underwent radiation therapy followed by chemotherapy with cisplatin and etoposide but died of tumor progression 15 months after his second hospitalization.
颅内成熟畸胎瘤复发为不同组织学类型的生殖细胞肿瘤的情况鲜有报道。作者描述了首例颅内成熟畸胎瘤恶变为卵黄囊瘤的病例,患者为一名16岁男孩,有1个月的厌食和嗜睡病史。此次发病前7年,该男孩曾接受手术切除成熟松果体畸胎瘤。第二次就诊时的计算机断层扫描图像显示第三脑室内有一个均匀强化的肿块。肿瘤被切除,组织学检查结果与卵黄囊瘤一致。切除术后,患者接受了放射治疗,随后用顺铂和依托泊苷进行化疗,但在第二次住院15个月后因肿瘤进展死亡。