Facial Plexiform Neurofibroma as an Intraparotid Nodule: A Rare Case Presentation
Neurofibromas of salivary gland are very rare and account for only 0.4% of all salivary gland neoplasms. Plexiform type of neurofibromas are predominantly seen in a scenario of neurofibromatosis-1 (NF-1) association, but solitary plexiform neurofibroma has also been occasionally reported. We present...
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Veröffentlicht in: | An International Journal of Otorhinolaryngology Clinics 2021-03, Vol.12 (1), p.8-10 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Neurofibromas of salivary gland are very rare and account for only 0.4% of all salivary gland neoplasms. Plexiform type of neurofibromas are predominantly seen in a scenario of neurofibromatosis-1 (NF-1) association, but solitary plexiform neurofibroma has also been occasionally reported. We present a report of this variant in a 17-year-old male who is presented with a slow-growing painless swelling in the right preauricular region for 8-month duration. Microscopic examination revealed multiple cell types including Schwann cells, perineurial cells, axons, lymphocytes, mast cells, and endoneurial fibroblasts. Immunostaining with S100 confirmed the neural origin.
How to cite this article:
Qadri S, Rabindranath D, Quadri S,
et al
. Facial Plexiform Neurofibroma as an Intraparotid Nodule: A Rare Case Presentation. Int J Otorhinolaryngol Clin 2020;12(1):8–10. |
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ISSN: | 0975-444X 0975-6957 |
DOI: | 10.5005/jp-journals-10003-1344 |