Sinonasal paraganglioma: Endoscopic resection with 4-year follow-up

Debbie A. Mouadeb, Rakesh K. Chandra, David W. Kennedy, Michael Feldman

Research output: Contribution to journalArticle

12 Scopus citations

Abstract

Background. Paragangliomas are uncommon neuroendocrine tumors. In the head and neck, they are most commonly seen at the carotid body, the temporal bone, or along the vagus nerve. Sinonasal paragangliomas are extremely rare. Most cases reported describe management by open surgical resection, with sublabial and/or transfacial approaches. Methods. We present a case of a large sinonasal paraganglioma successfully managed by endoscopic resection. Results. The patient has no evidence of recurrence after 4 years of follow-up. Conclusions. This case demonstrates that sinonasal paragangliomas might be amenable to endoscopic resection. However, the most important priority to consider when selecting a surgical technique is whether adequate excision with clear margins can be obtained. Furthermore, because of the aggressive nature of these tumors, regardless of the surgical approach, long-term follow-up is recommended.

Original languageEnglish (US)
Pages (from-to)1077-1081
Number of pages5
JournalHead and Neck
Volume25
Issue number12
DOIs
StatePublished - Dec 1 2003
Externally publishedYes

Keywords

  • Nasal cavity tumors
  • Sinonasal paraganglioma

ASJC Scopus subject areas

  • Otorhinolaryngology

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