Plexiform neurofibroma: An uncommon cause of conductive-type hearing loss

Abstract

Plexiform neurofibromas (PNs) are slow-growing, vascularised, limited, non-capsular benign tumours. They may cause functional impairments, cosmetic problems, and issues with pain or a sense of pressure. Involvement of the external ear canal, which can trigger conductive-type hearing loss and cosmetic problems, is rare. A 14-year-old male diagnosed with, and under follow-up for, type 1 neurofibromatosis presented with hearing loss and an auricle deformity caused by a mass on the postauricular region of the mastoid bone. This mass had grown gradually over the past 5 years and at the time of consultation completely filled the external ear canal, pushing the auricle forward. It was surgically removed. Postoperative histological examination allowed diagnosis of a plexiform neurofibroma. The external ear canal was successfully cleared, affording a good cosmetic outcome. Audiometric tests revealed that the airbone gap had closed.

Solitary Neurofibroma of External Aural Canal

“…Neurofibromas of the external auditory canal are rare [5]. It may be isolated or occur in the context of neurofibromatosis type I [6] [7] [8]. Isolated neurofibromas are called solitary neurofibromas.…”

“…Neurofibromas of the external auditory canal are rare [5]. It is often associated with neurofibromatosis type 1 (NF1) [6] [7]. Neurofibromatosis is one of the most commun ge-Int.…”