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Clinical features and management of intracranial subependymomas in children
Zonggang Hou1, Zhen Wu, Junting Zhang
1Beijing Neurosurgical Institute, Capital Medical University, Tiantan Xili 6, Dongcheng District, Beijing 100050, China.
Insights
Subependymomas are rare brain tumors in children. Surgical resection is the optimal treatment, leading to good outcomes and no recurrence in a study of five pediatric patients.
Area of Science:
- Neuro-oncology
- Pediatric Neurosurgery
- Central Nervous System Tumors
Background:
- Subependymoma is a rare, low-grade glioma affecting the central nervous system.
- It predominantly occurs in middle-aged and elderly men, with rare occurrences reported in children.
- Limited data exists on pediatric intracranial subependymoma.
Purpose of the Study:
- To retrospectively analyze the clinical characteristics and management of pediatric intracranial subependymoma.
- To summarize outcomes following surgical intervention in children diagnosed with this rare tumor.
Main Methods:
- Retrospective analysis of five pediatric patients diagnosed with intracranial subependymoma between July 1998 and April 2009.
- Review of clinical data, tumor location, surgical approach, and patient outcomes.
Main Results:
- Five pediatric patients (4 males, 1 female; mean age 8.6 years) were included.
- Intracranial hypertension was the most common presenting symptom.
- Tumor locations varied, including the fourth ventricle, cerebellopontine angle (CPA), and left parietal lobe.
- All patients underwent surgery with either total (3 patients) or subtotal (2 patients) resection.
- All patients achieved good outcomes without recurrence.
Conclusions:
- Surgery is the optimal therapeutic approach for pediatric intracranial subependymoma.
- Prompt surgical intervention leads to favorable outcomes and no recurrence in pediatric cases.
- Further research into rare pediatric central nervous system tumors like subependymoma is warranted.
Abstract:
Subependymoma is a rare low-grade glioma of the central nervous system that occurs most commonly in middle-aged and elderly men and rarely in children. Only a few paediatric patients with subependymomas have been reported. The authors retrospectively analysed five paediatric patients (4 males and 1 female; mean age 8.6 years; age range 5-13 years) at a single institute from July 1998 to April 2009 and summarised the clinical characteristics and management of paediatric intracranial subependymoma. The most common symptom in these five paediatric patients with subependymoma was intracranial hypertension. The tumours were located in the fourth ventricle in two patients, in the fourth ventricle with extension to the cerebellopontine angle (CPA) in one patient; in the right CPA exclusively in one patient, and intraparenchymally in the left parietal lobe in one patient, the latter two of which are rare locations for subependymoma. Surgery was performed on all five patients. The surgical approach was selected as appropriate for the tumor location. Total resection was achieved in three patients, and subtotal resection in two. All five patients had good outcomes without recurrence. We conclude that surgery is the optimal therapy for paediatric patients with intracranial subependymoma.
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