2018
DOI: 10.1093/neuonc/noy151
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Uncommon low-grade brain tumors

Abstract: An initial search of PubMed used broad search terms 'brain tumors', 'low-grade', 'radiotherapy, 'chemotherapy', 'surgery' and 'treatment' from January 1990 to March 2018. A subsequent focused search was undertaken using the names of individual histological subtypes of low-grade brain tumors as in the 2016 WHO classification. Only papers published in English were reviewed. The final reference list was generated on the basis of originality and relevance to the broad scope of this review.

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Cited by 10 publications
(6 citation statements)
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References 78 publications
(98 reference statements)
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“…The mechanism underlying the association between preNLR and severe peritumoral edema is complex and needs to be elucidated. Peritumoral edema has been described as a risk factor for early recurrence or progression and was the consequence of a disruption of the blood-brain barrier [ 27 , 28 ]. The reasons for preNLR value in predicting the occurrence and development of brain edema could be explained by neutrophil-induced neurotoxicity, increased capillary permeability, destruction of the BBB (Blood Brain Barrier), and cell swelling [29] , [30] , [31] .…”
Section: Discussionmentioning
confidence: 99%
“…The mechanism underlying the association between preNLR and severe peritumoral edema is complex and needs to be elucidated. Peritumoral edema has been described as a risk factor for early recurrence or progression and was the consequence of a disruption of the blood-brain barrier [ 27 , 28 ]. The reasons for preNLR value in predicting the occurrence and development of brain edema could be explained by neutrophil-induced neurotoxicity, increased capillary permeability, destruction of the BBB (Blood Brain Barrier), and cell swelling [29] , [30] , [31] .…”
Section: Discussionmentioning
confidence: 99%
“…Eosinophilic granular bodies and perivascular inflammation are often present. Typically, gangliogliomas align with a WHO grade 1 classification in the CNS [ 53 , 54 ].…”
Section: Gangliogliomamentioning
confidence: 99%
“…Ganglioglioma are benign (WHO grade I) [1] and rare well-differentiated and typically slow-growing mixed glioneuronal tumors composed of dysplastic mature ganglion cells and neoplastic glial cells with the highest incidence rates being in children and young adults, but they can occur at any age and anywhere in the central nervous system [2][3][4]. They are mainly characterized by a space-occupying lesion in the temporal and frontal lobes and are usually associated with chronic drug-resistant epilepsy [3][4][5]. The standard treatment is complete surgical resection [4,6], but even then ganglioglioma can develop a malignant transformation into anaplastic ganglioglioma (AGGL) classified as a grade III tumor [1,7].…”
Section: Introductionmentioning
confidence: 99%