Nail bed solitary neurofibroma: A case report and literature review

RATIONALE: Nail bed solitary neurofibroma is an extremely rare tumor, with only 9 cases recorded in the literature so far. PATIENT CONCERN: We present the case of a 42-year-old female patient, with a history of a slowly growing tumor in the nail bed of the left index and no clinical features of type I neurofibromatosis. DIAGNOSIS: Nail bed solitary neurofibroma. INTERVENTION: The tumor was surgically removed and the pathology examination established the diagnosis of neurofibroma. OUTCOMES: The postoperative outcome was good, with no recurrence 12 months after surgery. LESSONS: We present the rarity of this type of tumor localized in the nail bed, taking into consideration the only 9 cases recorded in the literature. Nail bed solitary neurofibroma should be also included in the differential diagnosis of a nail bed tumor.