Cerebellar glioblastoma in an NF1 patient. Is it surgical debulking really necessary?

被引:4
|
作者
Flower, Hannah [1 ]
Gallo, Pasquele [1 ,2 ,3 ]
机构
[1] Univ Edinburgh, Med Sch, Edinburgh, Midlothian, Scotland
[2] Western Gen Hosp, Edinburgh, Midlothian, Scotland
[3] Royal Hosp Sick Children, Edinburgh, Midlothian, Scotland
关键词
Cerebellar glioblastoma; NF1; MGMT methylation; Temozolomide; NEUROFIBROMATOSIS TYPE-1; MOYAMOYA SYNDROME; MULTIFORME; ADULT; CHILD;
D O I
10.1080/02688697.2019.1690127
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Neurofibromatosis type 1 is an autosomal dominant tumour syndrome with an increased risk of developing central nervous system neoplasms, mostly benign low-grade gliomas involving the optic pathway and the brainstem. High-grade astrocytomas or glioblastoma multiforme (GBM) are rare. Cerebellar GBMs are rarer still, only seven cases NF1 patients have been reported Case description: We report a case of a cerebellar GBM in a 25-year-old male with NF1 who survived 18 months from the initial diagnosis without surgical debulking but only chemo and radiotherapy. Conclusion: A literature review found that the best outcomes were achieved in NF1 patients who didn't undergo gross surgical resection. Possible reasons and future directions are discussed.
引用
收藏
页码:669 / 671
页数:3
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