Department of Oncology, Rigshospitalet, Denmark.
Acta Oncol. 2012 Jan;51(1):3-9. doi: 10.3109/0284186X.2011.586000.
Intracranial germ cell tumours (icGCTs) represent 3-15% of primary paediatric intracranial neoplasms with a considerable geographical variation in incidence. Ninety percent of patients diagnosed with icGCTs are under 20 years of age.
Histologic characteristics and investigation of the tumour markers β-human chorionic gonadotropin (β-hCG) and alpha-fetoprotein (AFP) help define the different categories of icGCTs. The tumours are divided into two major groups called germinomas and non-germinomatous GCTs (NGGCTs).
The clinical symptoms depend on the size and location of tumour in the brain, which is most commonly in the pineal or suprasellar region. Pineal GCTs often present with neurological symptoms because of their tendency to cause increased intracranial pressure. Suprasellar GCTs are often accompanied by endocrine abnormalities such as diabetes insipidus (DI), growth retardation and precocious or delayed puberty.
A combination of clinical findings, endocrine and tumour marker evaluation, spinal fluid cytology, magnetic resonance imaging (MRI) and biopsy helps verifying the diagnosis of an icGCT. A summary of published data (n = 97) revealed that >90% of patients at diagnosis had at least one endocrine abnormality, DI being the most common (>80%).
Classification of tumour is important for choice of treatment and for prognosis. A combination of chemotherapy and radiotherapy is often used, since most icGCTs have a great sensitivity to these treatment modalities.
Endocrine symptoms are very frequently appearing in patients with icGCTs and they can present long before neuroimaging verification of tumour is possible. It is of the outmost importance to have the diagnosis of icGCTs in mind when children, adolescents and young adults are presenting with endocrine irregularities, because most icGCTs are very sensitive to radiotherapy and chemotherapy, and early onset of treatment is important in order to minimize morbidity and mortality.
颅内生殖细胞瘤(icGCTs)占儿童原发性颅内肿瘤的 3-15%,发病率存在相当大的地域差异。90%诊断为 icGCTs 的患者年龄在 20 岁以下。
组织学特征和肿瘤标志物β-人绒毛膜促性腺激素(β-hCG)和甲胎蛋白(AFP)的检测有助于确定 icGCTs 的不同类别。肿瘤分为两大主要类型,称为生殖细胞瘤和非生殖细胞瘤生殖细胞瘤(NGGCTs)。
临床症状取决于肿瘤在大脑中的大小和位置,最常见于松果体或鞍上区。松果体生殖细胞瘤常因引起颅内压增高而出现神经系统症状。鞍上生殖细胞瘤常伴有内分泌异常,如尿崩症(DI)、生长迟缓、性早熟或青春期延迟。
临床发现、内分泌和肿瘤标志物评估、脑脊液细胞学、磁共振成像(MRI)和活检的综合运用有助于确诊 icGCT。对已发表数据(n=97)的总结显示,>90%的患者在诊断时至少存在一种内分泌异常,DI 最常见(>80%)。
肿瘤分类对治疗选择和预后都很重要。化疗和放疗的联合通常用于治疗,因为大多数 icGCTs 对这些治疗方法非常敏感。
内分泌症状在 icGCTs 患者中非常常见,并且在肿瘤的神经影像学证实之前很久就可能出现。当儿童、青少年和年轻人出现内分泌紊乱时,首先要考虑 icGCTs 的诊断,因为大多数 icGCTs 对放疗和化疗非常敏感,早期开始治疗对于降低发病率和死亡率非常重要。