University of Washington - Department of Neurological Surgery
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Schwannoma

Schwannomas are nerve sheath tumors. They are lobulated, grossly encapsulated tumors that often show cystic degeneration, hemorrhage and xanthomatous changes. Schwannomas arise eccentrically from their parent nerve. There is a slight female predominance and they are primarily seen in middle-aged adults. Most Schwannomas arise from dorsal sensory roots. They almost never become malignant.

Location : - intradural extramedullary
- combined intradural and extradural
- extradural
- intramedullary
70%
15%
15%
<1%

Pathology : - Antoni type A: densely packed, highly ordered spindle cells
- Antoni type B: loosely textured myxoid stroma

Therapy : treatment is surgical excision, which is usually curative. Postoperative radiotherapy may be considered for malignant Schwannomas

* Click to view The Case Presentations
Extradural Lumbar Schwannoma- Intradural Cervical Schwannoma-
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