Nail bed solitary neurofibroma: A case report and literature review
Mihaela Pertea1, Oxana-Mădălina Grosu1, Cristina Terinte2
1Clinic of Plastic Surgery, Emergency Hospital "Sf. Spiridon", University of Medicine and Pharmacy "Gr. T. Popa".
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.
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