Neurofibromas are relatively common lesions of
the nervous system, but only a few cases involving the pinna have been reported. Isolated neurofibroma of pinna without neurofibromatosis
has not been reported in the literature so far. Neurofibromas may develop anywhere
in the body, including cranial
and peripheral nerves. The type of impairment associated with neurofibromas depends
largely on the site of the lesion. Cutaneous lesions, especially in the head and
neck, generally cause deformity,
whereas lesions that affect deeper systems (e.g., the auditory and ocular systems)
are more likely to cause functional impairment. Usually found in individuals with neurofibromatosis, we report a case of neurofibroma of pinna in a patient
Cite this paper
Singh, S. , Tandon, S. , Lahiri, A. and Sharma, S. (2014) Neurofibroma of the Pinna. International Journal of Otolaryngology and Head & Neck Surgery
, 66-70. doi: 10.4236/ijohns.2014.32014
 David Muir et al. (2003) Tumorigenic Properties of Neurofibromin-Deficient Neurofibroma Schwann Cells. American Journal of Pathology, 158, 501-513.
 Griffith, B.H., et al. (1972) Von Rcklinnghausen’s Disease in Children. Plastic Reconstruction Surgery, 49, 647-653.http://dx.doi.org/10.1097/00006534-197206000-00012
 Kemph et al. (1995) Diagnostic and Clinical Outcome of Neurogenic Tumours in the Head and Neck Area. ORL: Journal for Oto-Rhino-Laryngology, 57, 273-278. http://dx.doi.org/10.1159/000276757
 Trevisani, T.P., Pohl, A.L. and Matloub, H.S. (1982) Neurofibroma of the Ear. Function and Aesthetics. Plastic Reconstructive Surgery, 70, 217-219. http://dx.doi.org/10.1097/00006534-198208000-00019
 Menick, F.J. (1990) Reconstruction of the Ear after Tumour Excision. Clinics in Plastic Surgery, 17, 405-415.
 Shaida, A.M. and Yung, M.W. (2007) Neurofibroma of the Pinna. Ear Nose Throat Journal, 86, 36-37, 44.