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An Orthotopic Sciatic Nerve Xenograft for Neurofibromatosis Type 1 Neurofibromas
Published on: October 10, 2025
Laryngeal plexiform neurofibroma in a child
Fikret Kasapoglu1, Talip Ozdemircan, Levent Erisen
1Department of Otorhinolaryngology, Uludag University Faculty of Medicine, Izmir Yolu Uzeri, 10659 Nilufer, Bursa, Gorukle 16059, Turkey. fkasapoglu@uludag.edu.tr
Ear, Nose, & Throat Journal
|June 20, 2013
Summary
Neurofibromatosis (NF) is a rare genetic disorder. This case report highlights laryngeal neurofibroma as a cause of airway obstruction in children, emphasizing its inclusion in differential diagnoses for respiratory distress.
Area of Science:
- Genetics
- Pediatric Medicine
- Oncology
Background:
- Neurofibromatosis (NF) is an autosomal dominant genetic disorder.
- Characterized by cafe au lait spots, neurofibromas, and Lisch nodules.
- NF can arise from neural tissue at any age.
Observation:
- A 5-year-old child presented with stridor and dyspnea.
- The child was diagnosed with a laryngeal plexiform neurofibroma.
- Laryngeal neurofibroma is an extremely rare manifestation of NF.
Findings:
- Plexiform neurofibroma in the larynx can cause significant airway obstruction.
- Symptoms include stridor and dyspnea, mimicking other pediatric respiratory conditions.
- Early diagnosis is crucial for effective management.
Implications:
- Laryngeal neurofibroma should be considered in the differential diagnosis of pediatric dyspnea.
- Increased awareness can lead to earlier detection and intervention.
- This case underscores the diverse clinical presentations of Neurofibromatosis.
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