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
下载
收藏
页码:669 / 671
页数:3
相关论文
共 50 条
  • [1] Brainstem Glioblastoma Multiforme in a Patient with NF1
    Fortunato, John T.
    Reys, Brian
    Singh, Pawan
    Pan, Edward
    ANTICANCER RESEARCH, 2018, 38 (08) : 4897 - 4900
  • [2] NF1 MOSAICISM IN A CMMRD-PATIENT WITH A GLIOBLASTOMA
    Guerrini-Rousseau, Lea
    Cabaret, Odile
    Muleris, Martine
    Vidaud, Dominique
    Cotteret, Sophie
    Rouleau, Etienne
    de Beaumais, Tiphaine Adam
    Varlet, Pascale
    Morscher, Raphael
    Abbou, Samuel
    Dufour, Christelle
    Brugieres, Laurence
    Grill, Jacques
    NEURO-ONCOLOGY, 2022, 24 : 69 - 70
  • [3] Management of glioblastoma in an NF1 patient with moyamoya syndrome: a case report
    Hideyuki Arita
    Yoshitaka Narita
    Makoto Ohno
    Yasuji Miyakita
    Yoshiko Okita
    Takafumi Ide
    Soichiro Shibui
    Child's Nervous System, 2013, 29 : 341 - 345
  • [4] Management of glioblastoma in an NF1 patient with moyamoya syndrome: a case report
    Arita, Hideyuki
    Narita, Yoshitaka
    Ohno, Makoto
    Miyakita, Yasuji
    Okita, Yoshiko
    Ide, Takafumi
    Shibui, Soichiro
    CHILDS NERVOUS SYSTEM, 2013, 29 (02) : 341 - 345
  • [5] A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma
    Seo, Yoorim
    Jeong, Yeonjeong
    Kim, Dong Yoon
    Choi, Kyueun
    Kim, Eun Sook
    Moon, Sung Dae
    Han, Je Ho
    KOREAN JOURNAL OF INTERNAL MEDICINE, 2018, 33 (01): : 214 - 217
  • [6] Cerebellar gliomas in children with NF1: pathology and surgery
    M. Vinchon
    Gustavo Soto-Ares
    Marie-Madeleine Ruchoux
    Patrick Dhellemmes
    Child's Nervous System, 2000, 16 : 417 - 420
  • [7] Cerebellar gliomas in children with NF1: pathology and surgery
    Vinchon, M
    Soto-Ares, G
    Ruchoux, MM
    Dhellemmes, P
    CHILDS NERVOUS SYSTEM, 2000, 16 (07) : 417 - 420
  • [8] Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma
    Origone, P
    Defferrari, R
    Mazzocco, K
    Lo Cunsolo, C
    De Bernardi, B
    Tonini, GP
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 118A (04): : 309 - 313
  • [9] Intraocular Ganglioneuroma In A Patient With NF1
    Harmsen, Hannah
    Mobley, Bret
    Abel, Ty
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2019, 78 (06): : 546 - 546
  • [10] Recurrent NF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)
    Buske, A
    Gewies, A
    Lehmann, R
    Rüther, K
    Algermissen, B
    Nürnberg, P
    Tinschert, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 86 (04): : 328 - 330