Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Neurofibroma is a benign nerve‑sheath tumor of the peripheral nervous system. In 90% of cases, they occur as isolated tumors without associated genetic disorders. However, the remaining cases are found in individuals with neurofibromatosis type I (NF1), an autosomal‑dominant inherited disorder. They can cause a range of symptoms, from physical disfigurement and pain to cognitive impairment.

Neurofibromas may measure 2 to 20 mm in diameter, are soft, flaccid, and pinkish‑white. A biopsy can be performed for histopathologic diagnosis.

Neurofibromas typically arise during the teenage years, often after puberty. In individuals with neurofibromatosis type I, they tend to increase in number and size throughout adulthood.

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  • Neurofibroma of the patient with neurofibromatosis.
  • Neurofibromas tend to worsen with age. The lesions in this individual first appeared when he was a teenager.
  • A solitary neurofibroma appears as a soft, erythematous papule.
References Neurofibroma 30969529 
NIH
Neurofibromas are the most prevalent benign peripheral nerve sheath tumor. Often appearing as a soft, skin-colored papule or small subcutaneous nodule, they arise from endoneurium and the connective tissues of peripheral nerve sheaths.