Results 21 to 30 of about 7,310 (199)
Diffusion, Perfusion, and Histopathologic Characteristics of Desmoplastic Infantile Ganglioglioma. [PDF]
, 2016 We present a case series of a rare tumor, the desmoplastic infantile ganglioglioma (DIG) with MRI diffusion and perfusion imaging quantification as well as histopathologic characterization. Four cases with pathologically-proven DIG had diffusion weighted
Bonnin, Jose +3 more
core +1 more source
Journal of Spinal Surgery, 2016 Gangliogliomas are relatively rare primary tumors of the central nervous system (CNS). It may occur throughout the CNS, predominantly the supratentorial area. Spinal cord ganglioglioma is a very rare entity. Majority of spinal gangliogliomas occur in the
B V Sandeep +3 more
doaj +1 more source
Seizure outcomes and prognostic factors in patients with gangliogliomas associated with epilepsy
Frontiers in Surgery, 2022 IntroductionGanglioglioma (GG) patients often present with seizures. Although most patients can be seizure-free after tumor resection, some still experience seizures. The present study aimed to analyze a group of GGs patients associated with epilepsy and
Yue Hu +14 more
doaj +1 more source
Tomography, 2022 Gangliogliomas are uncommon intracranial tumors that include neoplastic and abnormal ganglion cells, and show positive immunohistochemical staining for GFAP and syn.
Shaoguang Li +6 more
doaj +1 more source
Desmoplastic infantile ganglioglioma
The Pan African Medical Journal, 2019 The term desmoplastic infantile ganglioglioma was coined by VandenBerg et al in 1987. In their first report these authors referred to a rare, distinct brain tumor.
Salma Kamoun +4 more
doaj +1 more source
Cervicomedullary Ganglioglioma in a Child – A Case Report
Prague Medical Report, 2018 Ganglioglioma is a benign slow-growing neoplasm that most frequently occurs at the supratentorial region. Nevertheless, there are occasional reports of ganglioglioma occurring in the brainstem and spinal cord.
Eshagh Bahrami +2 more
doaj +1 more source
IDH1 mutant negative ganglioglioma progression to gliosarcoma
Interdisciplinary Neurosurgery, 2017 Gangliogliomas comprise of less than 1% of all primary brain tumours. Malignant transformation is rare. Correspondingly, secondary gliosarcomas, especially in the absence of previous irradiation exposure is too, exceedingly rare. Recent evidence supports
Liming Qiu +7 more
doaj +1 more source
Archives of the Balkan Medical Union, 2021 Introduction. Ganglioglioma represents a rare neuroglial tumour, affecting most frequently the pediatric population and arising in the temporal lobe. Based on the Ki67 proliferation index, gangliogliomas can be divided into benign and anaplastic.
Antonia C. LISIEVICI +6 more
doaj +1 more source
Frontiers in Pediatrics, 2021 Background: A ganglioglioma (GG), a tumor with both neuronal and astrocytic components, rarely occurs outside the central nervous system.Case Summary: We present the first reported case of a 1-month-old male with a congenital nasopharyngeal GG, nasal ...
He Zhao, Zhiwei Cao, Zhaowei Gu
doaj +1 more source
Comprehensive molecular characterisation of epilepsy-associated glioneuronal tumours [PDF]
, 2017 Glioneuronal tumours are an important cause of treatment-resistant epilepsy. Subtypes of tumour are often poorly discriminated by histological features and may be difficult to diagnose due to a lack of robust diagnostic tools.
Apps, J +19 more
core +2 more sources