Calaminus G, Bamberg M, Baranzelli M C, Benoit Y, di Montezemolo L C, Fossati-Bellani F, Jürgens H, Kühl H J, Lenard H G, Curto M L
Children's Hospital, University of Düsseldorf, Germany.
Neuropediatrics. 1994 Feb;25(1):26-32. doi: 10.1055/s-2008-1071577.
Intracranial germ cell tumors are rare tumor entities in childhood and adolescents. Extra- and intracranial germ cell tumors are identical in their histologic pattern and occur in preferential midline localizations such as the pineal and the suprasellar region. Germ cell neoplasms show increasing incidence rates over the last 30 years. The majority of intracranial germ cell neoplasms are germinomas. About 90% of the patients with pure germinomas can be salvaged by radiotherapy alone according to modern protocols. Non-germinomatous malignant CNS-germ cell tumors are considered to have a poor prognosis. In order to improve the survival of patients affected by these tumors different treatment approaches adding chemotherapy to conventional surgery and radiotherapy have been initiated by various study groups throughout the world. Due to the rarity of these neoplasms only a very limited number of patients has been enrolled in each study. In 1993 an international working group on these tumors was established by the International Society of Pediatric Oncology (SIOP).
颅内生殖细胞肿瘤在儿童和青少年中是罕见的肿瘤类型。颅外和颅内生殖细胞肿瘤在组织学模式上相同,且好发于中线部位,如松果体区和鞍上区。在过去30年中,生殖细胞肿瘤的发病率呈上升趋势。大多数颅内生殖细胞肿瘤是生殖细胞瘤。根据现代方案,约90%的单纯生殖细胞瘤患者仅通过放疗即可治愈。非生殖细胞性恶性中枢神经系统生殖细胞肿瘤被认为预后较差。为了提高这些肿瘤患者的生存率,世界各地的不同研究小组已启动了不同的治疗方法,即在传统手术和放疗的基础上加用化疗。由于这些肿瘤非常罕见,每项研究纳入的患者数量非常有限。1993年,国际小儿肿瘤学会(SIOP)成立了一个关于这些肿瘤的国际工作组。