» Articles » PMID: 36910263

The Clinicopathological Features of Ganglioglioma with CD34 Expression and BRAF Mutation in Patients with Epilepsy

Overview
Specialty Molecular Biology
Date 2023 Mar 13
PMID 36910263
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The aim of the study was to evaluate the clinicopathological features, as well as the surgical prognosis, of epilepsy-associated gangliogliomas (GG) with CD34 expression and BRAF mutation.

Methods: Clinical data of patients who underwent epilepsy surgery for GG were retrospectively studied. Univariate and multivariate analyses were performed to evaluate the correlations of clinical and pathological factors with molecular markers of CD34 expression and BRAF mutation in GG.

Results: A total of 208 patients with GG had immunohistochemical detection of CD34 expression (positive/negative: 184/24), and among them, 89 patients had immunohistochemical detection of BRAF mutation (positive/negative: 54/35). By univariate and multivariate analyses, seizure aura ( = 0.025), concordance of ictal electroencephalogram (EEG) findings ( = 0.045) and medial temporal tumor ( = 0.030) were found to be related to CD34 expression, but only hospitalization time ( = 0.042) was different for BRAF-mutated status. In addition, drug-resistant epilepsy ( = 0.040) and concordance of interictal EEG findings ( = 0.009) were found to be associated with tumor progression-free survival (PFS) in univariate analysis, but only concordance of interictal EEG findings was with significance in multivariate analysis. However, CD34 expression or BRAF mutation in GG was not found to be associated with surgical outcomes of seizure control and tumor PFS.

Conclusion: The CD34 expression or BRAF mutation in GG may partly influence the distribution of clinicopathological features of patients with epilepsy, but they may be not able to predict the surgical prognosis of seizure outcome and tumor recurrence.

Citing Articles

Pediatric cerebral ganglioglioma epilepsy surgery: enhancing seizure outcomes through optimized resection applying high-field intraoperative magnetic resonance imaging.

Kurzbuch A, Cooper B, Kitchen J, McLaren A, Tronnier V, Ellenbogen J Childs Nerv Syst. 2025; 41(1):110.

PMID: 39934322 DOI: 10.1007/s00381-025-06766-9.

References
1.
Koelsche C, Wohrer A, Jeibmann A, Schittenhelm J, Schindler G, Preusser M . Mutant BRAF V600E protein in ganglioglioma is predominantly expressed by neuronal tumor cells. Acta Neuropathol. 2013; 125(6):891-900. DOI: 10.1007/s00401-013-1100-2. View

2.
Zaky W, Patil S, Park M, Liu D, Wang W, Wani K . Ganglioglioma in children and young adults: single institution experience and review of the literature. J Neurooncol. 2018; 139(3):739-747. DOI: 10.1007/s11060-018-2921-6. View

3.
Slegers R, Blumcke I . Low-grade developmental and epilepsy associated brain tumors: a critical update 2020. Acta Neuropathol Commun. 2020; 8(1):27. PMC: 7063704. DOI: 10.1186/s40478-020-00904-x. View

4.
Deb P, Sharma M, Tripathi M, Chandra P, Gupta A, Sarkar C . Expression of CD34 as a novel marker for glioneuronal lesions associated with chronic intractable epilepsy. Neuropathol Appl Neurobiol. 2006; 32(5):461-8. DOI: 10.1111/j.1365-2990.2006.00734.x. View

5.
Sidney L, Branch M, Dunphy S, Dua H, Hopkinson A . Concise review: evidence for CD34 as a common marker for diverse progenitors. Stem Cells. 2014; 32(6):1380-9. PMC: 4260088. DOI: 10.1002/stem.1661. View