Lowis S P, Pizer B L, Coakham H, Nelson R J, Bouffet E
Bristol Royal Hospital for Sick Children, UK.
Childs Nerv Syst. 1998 Jul;14(7):317-21. doi: 10.1007/s003810050233.
Standard treatment of spinal cord astrocytomas is based upon surgery, followed by radiotherapy when resection is incomplete or when histology is of high grade. Owing to the major consequences of radiotherapy on the spine in childhood, alternative therapies must be explored. The potential role of chemotherapy in the management of spinal cord astrocytoma remains to be defined. Two patients are described. The first was a 19-month-old child with an anaplastic astrocytoma of the cervical spinal cord that progressed rapidly after initial partial resection. Chemotherapy was begun according to the UKCCSG Baby Brain Protocol, with marked clinical improvement. Reassessment by MRI at 4 months showed improvement, and at the end of treatment no evaluable disease remained. The second was a 4-year-old child with a recurrent low-grade astrocytoma. Chemotherapy according to the SIOP Protocol for Low Grade Gliomas was administered for 3 months, after which marked tumour regression was seen, with neurological recovery. These patients demonstrate the potential value and low morbidity of chemotherapy in spinal cord astrocytoma. The management of this rare tumour is discussed.
脊髓星形细胞瘤的标准治疗方法是手术,若切除不完全或组织学分级为高级别,则术后进行放疗。由于放疗对儿童脊柱有重大影响,必须探索替代疗法。化疗在脊髓星形细胞瘤治疗中的潜在作用仍有待确定。本文描述了两名患者。第一名是一名19个月大的儿童,患有颈髓间变性星形细胞瘤,初次部分切除后病情迅速进展。根据英国儿童癌症研究组婴儿脑肿瘤方案开始化疗,临床症状明显改善。4个月时通过磁共振成像重新评估显示病情好转,治疗结束时无可评估的疾病残留。第二名是一名4岁儿童,患有复发性低级别星形细胞瘤。根据国际小儿肿瘤学会低级别胶质瘤方案进行了3个月的化疗,之后肿瘤明显消退,神经功能恢复。这些患者证明了化疗在脊髓星形细胞瘤治疗中的潜在价值和低发病率。本文还讨论了这种罕见肿瘤的治疗方法。