A neurofibroma can arise with no known cause, or it may appear in people with a genetic condition called neurofibromatosis type 1. These tumors are most often found in people ages 20 to 40 years.
Your health care provider will look at several factors to diagnose a neurofibroma. These may include a physical exam, your medical history, and the results of an imaging test such as a CT or MRI scan.
Imaging studies can help pinpoint where the tumor is, find very small tumors, and identify what tissues are affected or nearby. You may undergo a PET scan to get an indication of whether the tumor is benign. You also may have a biopsy done by a radiologist before surgery to diagnose the mass as being a neurofibroma.