Chordoma | Craniopharyngioma | Epidermoid Cyst | Glioma | Hemangioblastoma | Meningioma | Metastatic Brain Tumors | Olfactory Neuroblastoma | SchwannomaSphenoid Sinus Cancer

Schwannoma

OVERVIEW:

These tumors are typically benign and arise from the nerve sheath (covering) of cranial nerves along-side the cerebellum and brainstem. The most common schwannoma arises from the 8th cranial nerve (the vestibulo-cochlear nerve) or the 5th cranial nerve (the trigeminal nerve). In some instances, schwannomas are related to a genetic syndrome called Neurofibromatosis. Bilateral vestibular schwannomas are associated with NF-2.

SYMPTOMS:

Vestibular (acoustic) schwannomas arise from the inferior vestibular nerve in the internal auditory canal and initially cause hearing loss and tinnitus (ringing in the ear). As they enlarge into the cerebello-pontine angle, they can compress the brainstem and other cranial nerves, resulting in loss of balance and coordination, vertigo, facial numbness, facial weakness and difficulty swallowing.

Trigeminal schwannomas are less common than acoustic schwannomas. They generally arise in Meckel’s cave in the skull base and the pre-pontine space. These tumors typically cause facial pain (trigeminal neuralgia). As they enlarge they can grow further into the cavernous sinus or into the posterior fossa, causing double vision, loss of coordination and other symptoms of brainstem compression.

DIAGNOSIS:

Schwannomas are typically diagnosed by an MRI with gadolinium or a CT scan of the brain. A focused MRI of the internal auditory canals is typically best for visualizing a vestibular schwannoma. Other tests may also be needed such as angiography (typically now performed as a CT angiogram or an MR angiogram) or an audiogram.

TREATMENT:

Treatment for vestibular (acoustic) schwannomas is by surgical removal through a retro-sigmoid craniotomy or other skull base approach or by radiosurgery. For tumors under 2.5 cm, either surgery or radiosurgery are reasonable treatment options. For tumors over 2.5 cm, surgical removal is generally recommended.

Treatment for trigeminal schwannomas is typically by surgical removal through a retro-sigmoid craniotomy or other skull base approach, depending upon the location.

In some patients with a vestibular or trigeminal schwannoma in whom only a sub-total tumor removal is possible, radiosurgery or stereotactic radiotherapy may be effectively used to control further tumor growth.


Chemotherapy is generally not used for treating schwannomas.