1. Adult hippocampal ganglioneuroblastoma: Case report and literature review.
- Author
-
Yao PS, Chen GR, Shang-Guan HC, Lin QS, Wang XF, Zheng SF, and Kang DZ
- Subjects
- Adolescent, Brain Neoplasms complications, Brain Neoplasms diagnostic imaging, Brain Neoplasms therapy, Combined Modality Therapy, Diagnosis, Differential, Ganglioneuroblastoma complications, Ganglioneuroblastoma diagnostic imaging, Ganglioneuroblastoma therapy, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Seizures etiology, Brain Neoplasms diagnosis, Ganglioneuroblastoma diagnosis
- Abstract
Rationale: Intracranial ganglioneuroblastoma represents a rare subtype of primitive neuroectodermal tumor. Here, we report a hippocampal ganglioneuroblastoma and a literature review of cerebral anglioneuroblastoma is carried out., Patient Concerns: We report a 16-year-old male patient presenting with absence seizure and high-infiltration hippocampal ganglioneuroblastoma., Interventions: Magnetic resonance imaging (MRI) indicates a space-occupying lesion with a well-defined margin in the right temporal lobe and hippocampus. However, hyper-signal on flair and diffusion-weighted imaging (DWI) with a low apparent diffusion coefficient (ADC) value is detected, which prompts high tumoral invasiveness., Interventions: A total resection of tumor and subsequent chemotherapy combing with radiotherapy is performed., Outcomes: For a follow-up period of 60 months, no evidence of recurrence and further seizures are detected., Lessons: High-infiltration hippocampal ganglioneuroblastoma is a rare event. MRI examination often showed features of low-grade gliomas, while hyper-signal lesion on DWI with a low ADC value can be detected. Complete resection combined with fractionated radiotherapy and chemotherapy was the optimal treatment for cerebral ganglioneuroblastoma., (Copyright © 2017 The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF