eMedicine Specialties > Dermatology > Diseases of the Oral Mucosa
Oral Neurofibroma: Follow-up
Updated: Oct 7, 2009
Follow-up
Further Outpatient Care
Solitary neurofibromas are treated by surgical excision and exhibit very low recurrence. The patient should be instructed to report any new growth seen in the area or any abnormal sensations, such as tingling. These signs may signify a recurrence, and lesions may require repeat excision.
Deterrence/Prevention
No special precaution is recommended for prevention of recurrence. Surgical excision is usually curative.
Complications
A possible, although extremely rare, complication may be recurrence of the lesion. Other potential complications that may be seen are purely associated with surgical treatment and may include scarring and numbness.
Prognosis
Usually, the prognosis for solitary neurofibroma is extremely good, with only rare instances of recurrence after resection; however, 5-15% exhibit malignant transformation of 1 or more lesions. This neurofibrosarcomatous change has an extremely poor prognosis, and distant metastasis is common. The average 5-year survival rate is only 15%.
Miscellaneous
Special Concerns
A solitary neurofibroma may be a precursor to neurofibromatosis (also see Neurofibromatosis, Type 1), and the patient should be evaluated with this in mind. Close clinical follow up and/or genetic testing may be required, especially if a lesion recurs multiple times or more than one lesion is seen.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous Chief Editor, William D. James, MD, to the development and writing of this article.
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References
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Further Reading
Keywords
oral neurofibroma, neurofibroma, neurofibromatosis, von Recklinghausen's disease of the skin, von Recklinghausen disease, fibroma molluscum
Follow-up: Oral Neurofibroma