Open Access

Sinonasal spindle cell carcinoma presenting with bilateral visual loss: A case report and review of the literature

  • Authors:
    • Tsung‑Wei Liu
    • Shih‑Han Hung
    • Po‑Yueh Chen
  • View Affiliations

  • Published online on: May 25, 2016     https://doi.org/10.3892/ol.2016.4620
  • Pages: 401-404
  • Copyright: © Liu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Spindle cell carcinoma (SpCC) is a rare variant of squamous cell carcinoma (SCC). SpCC of sinonasal origin is relatively rare and more aggressive than normal SCC. It most commonly involves the maxillary sinus, and rarely the sphenoid sinus. The present study reports a case of sphenoid sinus SpCC presenting with bilateral visual loss. Following endoscopic sinus decompression surgery, the patient was referred to the Oncology Department for a staging workup, and subsequently received concurrent chemoradiotherapy; however, the vision of the patient was not recovered, despite treatment. To the best of our knowledge, this is the first reported case of synchronous inverted papilloma of the sphenoid sinus and SpCC presenting with optic nerve compression.
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July-2016
Volume 12 Issue 1

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Copy and paste a formatted citation
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Spandidos Publications style
Liu TW, Hung SH and Chen PY: Sinonasal spindle cell carcinoma presenting with bilateral visual loss: A case report and review of the literature. Oncol Lett 12: 401-404, 2016
APA
Liu, T., Hung, S., & Chen, P. (2016). Sinonasal spindle cell carcinoma presenting with bilateral visual loss: A case report and review of the literature. Oncology Letters, 12, 401-404. https://doi.org/10.3892/ol.2016.4620
MLA
Liu, T., Hung, S., Chen, P."Sinonasal spindle cell carcinoma presenting with bilateral visual loss: A case report and review of the literature". Oncology Letters 12.1 (2016): 401-404.
Chicago
Liu, T., Hung, S., Chen, P."Sinonasal spindle cell carcinoma presenting with bilateral visual loss: A case report and review of the literature". Oncology Letters 12, no. 1 (2016): 401-404. https://doi.org/10.3892/ol.2016.4620