Neurofibromas can be removed surgically, and the outlook is generally favorable; however, individuals with neurofibromatosis may develop multiple tumors throughout their lifetime
Neurofibromas are noncancerous tumors that develop from cells in the nervous system. They are a characteristic feature of neurofibromatosis. Treatment may be necessary if the neurofibroma causes symptoms or complications. Regular monitoring is essential for individuals with neurofibromatosis to address emerging concerns and manage potential complications.
Benign tumors that originate from nerve tissue
Soft, rubbery bumps under the skin, skin discoloration, pain
Clinical evaluation, sometimes genetic testing
Variable, depends on specific type
Skin and neurological complications, potential for systemic issues
Genetic mutations, often associated with neurofibromatosis type 1 (NF1)
Monitoring for growth and complications, surgical removal if necessary
Monitoring for growth and complications, surgical removal if necessary
Genetic, various types including NF1 and NF2
Lifelong monitoring and management tailored to specific type
Please note that the information provided is based on the current understanding of these conditions and treatments may vary based on individual circumstances. Always consult with a healthcare provider for accurate information.
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