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  • Title: Laryngeal plexiform neurofibroma in a child.
    Author: Kasapoglu F, Ozdemircan T, Erisen L.
    Journal: Ear Nose Throat J; 2013 Jun; 92(6):E31. PubMed ID: 23780601.
    Abstract:
    Neurofibromatosis (NF) is a genetically inherited, autosomal dominant disease, characterized by multiple cafe au lait spots, cutaneous neurofibromas and "Lisch nodules." Neurofibromatosis can develop from a neural source at any age. However, neurofibroma of the larynx is extremely rare and is usually manifested by obstructive airway symptoms. We encountered a 5-year-old child presenting with stridor and dyspnea, who had a diagnosis of laryngeal plexiform neurofibroma. The purpose of our report is the consideration of laryngeal NF in the differential diagnosis of dyspnea in infants and children.
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