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Background: Stereotactic radiosurgery (SRS) is a potentially important option for intracranial ependymoma patients.
Objective: To analyze the outcomes of intracranial ependymoma patients who underwent SRS as a part of multimodality management.
Methods: Seven centers participating in the International Gamma Knife Research Foundation identified 89 intracranial ependymoma patients who underwent SRS (113 tumors). The median patient age was 16.3 yr (2.9-80). All patients underwent previous surgical resection and radiation therapy (RT) of their ependymomas and 40 underwent previous chemotherapy. Grade 2 ependymomas were present in 42 patients (52 tumors) and grade 3 ependymomas in 48 patients (61 tumors). The median tumor volume was 2.2 cc (0.03-36.8) and the median margin dose was 15 Gy (9-24).
Results: Forty-seven (53%) patients were alive and 42 (47%) patients died at the last follow-up. The overall survival after SRS was 86% at 1 yr, 50% at 3 yr, and 44% at 5 yr. Smaller total tumor volume was associated with longer overall survival (P = .006). Twenty-two patients (grade 2: n = 9, grade 3: n = 13) developed additional recurrent ependymomas in the craniospinal axis. The progression-free survival after SRS was 71% at 1 yr, 56% at 3 yr, and 48% at 5 yr. Adult age, female sex, and smaller tumor volume indicated significantly better progression-free survival. Symptomatic adverse radiation effects were seen in 7 patients (8%).
Conclusion: SRS provides another management option for residual or recurrent progressive intracranial ependymoma patients who have failed initial surgery and RT.
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http://dx.doi.org/10.1093/neuros/nyy082 | DOI Listing |
Asian J Neurosurg
September 2025
Department of Neurosurgery, Max Super Speciality Hospital, Vaishali, Ghaziabad, Uttar Pradesh, India.
Objective: Deeply located intracranial lesions such as intraparenchymal and intraventricular lesions are surgically challenging and associated with unavoidable complications such as seizure, surgical bed hematoma, and brain contusion caused by traction. The objective of this study is to evaluate the safety and effectiveness of the microscopic tubular retractor of a plastic syringe for the resection of deeply located brain lesions.
Materials And Methods: We retrospectively studied 157 patients with deep-seated intracranial lesions who underwent microscopic resection with the help of a tubular retractor made of a plastic syringe and Teflon introducer between January 2018 and January 2024 in a tertiary hospital.
Cureus
July 2025
Neurology Department, Agadir University Hospital, Agadir, MAR.
Neurofibromatosis type 2 (NF2) is a rare genetic disorder affecting the nervous system, primarily characterized by benign tumor formation, including bilateral vestibular schwannomas, meningiomas, and ependymomas. These tumors are collectively known as MISME (multiple intracranial schwannomas, meningiomas, and ependymomas) syndrome. We report a case of a 35-year-old woman with no notable medical or family history, who presented with progressive hearing loss and right upper limb weakness.
View Article and Find Full Text PDFNeurol Med Chir (Tokyo)
August 2025
Department of Neurosurgery, the University of Tokyo.
Ependymoma, a rare neuroepithelial malignancy of the central nervous system, affects both children and adults and may occur anywhere along the neuroaxis. This study aimed to analyze the treatment outcomes of adult intracranial ependymoma cases in Japan using data from the Brain Tumor Registry of Japan between 2001 and 2008. The dataset comprised 169 eligible patients after applying exclusion criteria, such as subependymoma and myxopapillary ependymoma cases.
View Article and Find Full Text PDFHum Pathol
August 2025
Department of Neurosurgery, Qilu Hospital of Shandong University and Institute of Brain and Brain-Inspired Science, Shandong University, Jinan, China; Shandong Key Laboratory of Brain Function Remodeling, Jinan, China. Electronic address:
Although anaplastic lymphoma kinase (ALK) gene fusions are increasingly recognized in newly classified pediatric high-grade gliomas, intracranial low-grade tumors harboring ALK rearrangements remain under characterized in the literature. Herein, we present five cases of low-grade intracranial tumors with ALK rearrangements that were diagnosed at a single institution over a continuous 24-month period. Comprehensive clinicopathological evaluation integrating morphological analysis, immunohistochemical profiling, and molecular characterization of fusion partners was performed.
View Article and Find Full Text PDFCureus
July 2025
General Practice, General Hospital, Umunze, NGA.
Myxopapillary ependymomas (MPEs) are rare, slow-growing spinal tumors that arise from the filum terminale and are classified as World Health Organization (WHO) Grade 2 tumors. They typically present with features of lower spinal cord or cauda equina compression, such as radiculopathy, limb weakness, or sphincter dysfunction. Presentation with features of increased intracranial pressure (IIP) is rare and has been reported in a few isolated cases.
View Article and Find Full Text PDF