• Ear Nose Throat J · Jun 2013

    Case Reports

    Laryngeal plexiform neurofibroma in a child.

    • Fikret Kasapoglu, Talip Ozdemircan, and Levent Erisen.
    • Department of Otorhinolaryngology, Uludag University Faculty of Medicine, Izmir Yolu Uzeri, 10659 Nilufer, Bursa, Gorukle 16059, Turkey. fkasapoglu@uludag.edu.tr
    • Ear Nose Throat J. 2013 Jun 1; 92 (6): E31.

    AbstractNeurofibromatosis (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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