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Oculomotor nerve schwannoma: a case report
Yong-Hwan Cho1, Kyung-Su Sung1, Young-Jin Song1
1Brain Tumor Institute Medical Science Research Center, College of Medicine, Dong-A University, Busan, Korea. ; Department of Neurosurgery, College of Medicine, Dong-A University, Busan, Korea.
Brain Tumor Research and Treatment
|June 14, 2014
Summary
Oculomotor schwannoma, a rare tumor of the oculomotor nerve, can cause vision problems. Surgical removal is effective, with symptoms gradually improving post-operation.
Area of Science:
- Neuro-oncology
- Ophthalmology
- Neurosurgery
Background:
- Schwannomas represent 8% of intracranial tumors, with 90% being vestibular schwannomas.
- Oculomotor schwannoma, particularly without neurofibromatosis, is exceptionally rare.
- Intracranial tumors can present with diverse neurological deficits.
Purpose of the Study:
- To report an extremely rare case of oculomotor schwannoma.
- To describe the clinical presentation, surgical management, and outcome of this rare tumor.
- To highlight the diagnostic and therapeutic challenges of atypical schwannomas.
Main Methods:
- A case study of a 41-year-old female with blurred vision.
- Diagnostic imaging using Brain Magnetic Resonance Imaging (MRI).
- Surgical intervention via a fronto-temporal approach with subtotal tumor removal under microscopic guidance.
Main Results:
- Brain MRI revealed an extra-axial mass in the left superior orbital fissure, originating from the oculomotor nerve.
- Pathological examination confirmed the mass as a schwannoma.
- Post-surgery, the patient experienced temporary ptosis and medial gaze limitation, which showed gradual improvement.
Conclusions:
- Oculomotor schwannoma is a rare diagnosis that requires prompt surgical intervention.
- Microscopic subtotal removal is a viable surgical strategy for oculomotor schwannoma.
- Despite potential postoperative deficits, functional recovery is often observed in patients with oculomotor schwannoma.

