Intracranial ganglioglioma WHO I: results in a series of eight patients treated with stereotactic interstitial brachytherapy.

J Neurooncol

Department of Stereotaxy and Functional Neurosurgery, Hospital of Cologne-Merheim, University of Witten/Herdecke, Ostmerheimer Strasse 200, 51109, Cologne, Germany.

Published: June 2014

In this retrospective study we evaluated the efficacy of interstitial brachytherapy (IBT) using (125)Iodine seeds ((125)I) for intracranial ganglioglioma WHO I. Between October 1994 and March 2010, eight patients (m/f = 5/3, median age 30.4 years, age range 7-42.5 years) with intracranial ganglioglioma WHO I were treated with IBT using stereotactically implanted (125)I seeds. The median follow-up time was 41.5 months (range 16.7-140.1 months). Prior to interstitial brachytherapy one patient underwent microsurgical resection for three times; seven patients were treated with IBT primarily. In all patients we implanted the (125)I seeds stereotactically guided. The cumulative tumor surface dose ranged between 50 and 65 Gy (permanent implantation) and the median tumor volume was 5.6 ml (range 0.9-26 ml). After brachytherapy, follow-up MR imaging revealed complete remission in one patient, partial remission in three and stable disease in the remaining four patients. Five of eight patients presented with seizures were either seizure-free (1/5) or improved (4/5). Temporary treatment-related morbidity occurred in one patient only (headache, nausea/vomiting) and resolved completely under steroid medication after 4 weeks. No treatment-related mortality was observed. This study indicates that interstitial brachytherapy for the treatment of intracranial ganglioglioma WHO I is safe and provides a high rate of local tumor control. Due to the limited number of cases, it is not possible to conduct a rigorous statistical evaluation. Thus, larger numbers of patients are required.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11060-014-1438-xDOI Listing

Publication Analysis

Top Keywords

intracranial ganglioglioma
16
interstitial brachytherapy
16
patients treated
8
treated ibt
8
implanted 125i
8
125i seeds
8
patients
7
brachytherapy
5
intracranial
4
ganglioglioma series
4

Similar Publications

and () gene fusion central nervous system (CNS) tumors are increasingly recognized as a potential distinct entity, with only limited reported cases. The imaging characteristics of these tumors have not been well established. In this study, we provide a detailed radiological description of a case in a 24‑year‑old man and conduct a literature review to identify common imaging features.

View Article and Find Full Text PDF

Gangliogliomas (GG) are rare primary central nervous system (CNS) tumors. These CNS tumors are more commonly located at the supratentorial level. The treatment of choice for these tumors is surgical resection, and the role of radiotherapy remains controversial.

View Article and Find Full Text PDF
Article Synopsis
  • - The article discusses a rare finding of atypical pathological features in the brains of patients with drug-resistant epilepsy, revealing a mix of ganglioglioma and focal cortical dysplasia, which hasn't been documented before.
  • - Comprehensive tests including histopathological staining and molecular genetic analysis were conducted, and MRI scans showed unusual patterns such as "transmantle" distribution and local alterations in the brain structure.
  • - The findings suggest the presence of a new subgroup of gangliogliomas characterized by cellular atypia, indicating a potential link between different types of neuronal-glial tumors that could reshape our understanding of epilepsy-related brain pathology.
View Article and Find Full Text PDF

Child Neurology: Simple Motor Tics Associated With Thalamic Ganglioglioma.

Neurology

December 2024

From the Department of Pediatric Neurology (Y.C.), Guizhou Branch of Shanghai Children's Medical Center of Shanghai Jiaotong University School of Medicine; Department of Pediatric Neurology (Y.C.), Guizhou Provincial People's Hospital; School of Public Heath (M.Y.), the Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang; and Department of Rehabilitation (H.Z.), Children's Hospital of Fudan University, Shanghai, China.

Tic disorders (TDs) include a heterogeneous group of neurodevelopmental conditions linked to dysfunction of the cortical-striatal-thalamic-cortical (CSTC) circuit. In this article, we report a case of a 9-year-old boy who presented with infrequent tics affecting the right eye and mouth. Brain imaging revealed a T2-weighted hyperintense mass in the left thalamus.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!