Neurilemoma

From WikiMD's Wellness Encyclopedia

Neurilemoma Neurilemoma, also known as schwannoma, is a benign tumor that arises from Schwann cells, which are the cells responsible for the myelin sheath covering peripheral nerves. This article provides a comprehensive overview of neurilemoma, including its etiology, clinical presentation, diagnosis, treatment, and prognosis.

Etiology[edit | edit source]

Neurilemomas are typically sporadic and arise from the Schwann cells of the peripheral nervous system. They are associated with the following factors:

Clinical Presentation[edit | edit source]

Patients with neurilemoma may present with a variety of symptoms depending on the location of the tumor:

Diagnosis[edit | edit source]

The diagnosis of neurilemoma involves a combination of clinical evaluation and imaging studies:

  • Magnetic Resonance Imaging (MRI): MRI is the preferred imaging modality, often showing a well-defined, encapsulated mass.
  • Biopsy: A biopsy may be performed to confirm the diagnosis, revealing spindle-shaped Schwann cells.

Treatment[edit | edit source]

The treatment of neurilemoma depends on the size, location, and symptoms:

  • Surgical Resection: The primary treatment is surgical removal, which is often curative.
  • Observation: In asymptomatic cases, especially in older patients, observation may be appropriate.

Prognosis[edit | edit source]

Neurilemomas are benign and have an excellent prognosis following complete surgical resection. Malignant transformation is rare.

See Also[edit | edit source]

External Links[edit | edit source]

NIH genetic and rare disease info[edit source]

Neurilemoma is a rare disease.

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Contributors: Prab R. Tumpati, MD