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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Laryngeal neurofibroma: case report of a child.

Neurofibromatosis is characterized by multiple café-au-lait spots and cutaneous neurofibromas. Laryngeal involvement in neurofibromatosis is rare and is usually manifested by obstructive airway symptoms. We encountered a 1 year 8-month-old girl who was a victim of neurofibromatosis with the presentation of stridor. Fiberoptic laryngoscopy revealed a round smooth mass over the right aryepiglottic fold which prolapsed into the larynx during inspiration. Carbon dioxide laser excision was performed and histopathologic examination revealed a plexiform neurofibroma. The patient had regular follow up for almost 4 years. Even though there seemed to be a recurrence, she remained symptom free.[1]

References

  1. Laryngeal neurofibroma: case report of a child. Chen, Y.C., Lee, K.S., Yang, C.C., Chang, K.C. Int. J. Pediatr. Otorhinolaryngol. (2002) [Pubmed]
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