Packer R J, Sutton L N, Rorke L B, Zimmerman R A, Littman P, Bruce D A, Schut L
Cancer. 1985 Jul 1;56(1):195-9. doi: 10.1002/1097-0142(19850701)56:1<195::aid-cncr2820560133>3.0.co;2-3.
Oligodendrogliomas are uncommon intracranial tumors of childhood, especially when these tumors arise in the posterior fossa. Oligodendrogliomas are usually treated with local radiation therapy. The authors report four children, median age 7.5 years, cared for over a 7-year period, who had oligodendrogliomas (all histologically malignant) of the cerebellar region. Three patients received local radiation therapy and all had recurrent disease at a median of 11 months posttreatment outside their radiation field; at the time of relapse, disease at the primary tumor site was stable. One child treated with craniospinal and local radiation therapy is disease-free 15 months after diagnosis. These results suggest that oligodendrogliomas of the posterior fossa should be considered potentially malignant lesions and treated with local plus presymptomatic craniospinal radiation therapy.
少突胶质细胞瘤是儿童期罕见的颅内肿瘤,尤其是当这些肿瘤发生于后颅窝时。少突胶质细胞瘤通常采用局部放射治疗。作者报告了4名儿童,中位年龄7.5岁,在7年期间接受治疗,他们患有小脑区域的少突胶质细胞瘤(所有组织学上为恶性)。3例患者接受了局部放射治疗,所有患者在治疗后中位11个月时在放射野外复发;复发时,原发肿瘤部位的疾病稳定。1名接受全脑全脊髓和局部放射治疗的儿童在诊断后15个月无疾病。这些结果表明,后颅窝少突胶质细胞瘤应被视为潜在的恶性病变,并采用局部加症状前全脑全脊髓放射治疗。