Solitary neurofibroma

Solitary Neurofibroma is a type of neurofibroma, a benign tumor that originates from the nervous system. It is characterized by the presence of a single, isolated tumor, unlike other types of neurofibromas which may present multiple tumors.

Overview

Neurofibromas are tumors that develop in the nervous system. They are typically benign, meaning they are not cancerous and do not spread to other parts of the body. Solitary neurofibromas are characterized by the presence of a single, isolated tumor. This distinguishes them from other types of neurofibromas, such as plexiform neurofibromas, which are characterized by multiple tumors.

Symptoms

The symptoms of solitary neurofibroma can vary depending on the location of the tumor. Common symptoms may include pain, numbness, or weakness in the affected area. In some cases, the tumor may be visible as a lump under the skin.

Diagnosis

Diagnosis of solitary neurofibroma typically involves a physical examination and imaging tests, such as MRI or CT scan. A biopsy may also be performed to confirm the diagnosis.

Treatment

Treatment for solitary neurofibroma often involves surgical removal of the tumor. In some cases, radiation therapy may also be used.

See Also

• Neurofibroma
• Plexiform neurofibroma
• Nervous system
• Tumor
• MRI
• CT scan
• Biopsy
• Radiation therapy

Solitary neurofibroma Resources
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