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Abstract
Synovial sarcoma of the larynx: case report and literature review. Synovial sarcoma is a rare mesenchymal malignancy which represents 8.5% of all soft tissue sarcomas and usually occurs in the lower extremities of young adults. Because the incidence in the head and neck region is very low, only 13 patients with endolaryngeal localisation have been reported so far. We present here a case of aryepiglottic synovial sarcoma. The tumour was completely resected, under suspension micro-laryngoscopy, using a CO2 laser. No recurrence was observed three years after the surgery. Complete surgical excision is the treatment of choice. The role of chemotherapy and radiotherapy is still debated. However, this tumour has a poor prognosis because of the occurrence of distant metastasis.
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Article Info
Published In
Journal
B-ENT
Volume / Issue
Volume 1 · Issue 1
Pages
47-51
History
Published Online
April 15, 2005
Affiliations
V. Boniver
Department of Otorhinolaryngology, Head and Neck Surgery, University of Liège, CHU Sart Tilman, Liège, Belgium
P. Moreau
ENT, Head and Neck Surgery Department, University Hospital Centre, Liège
Ph. Lefebvre
ENT Department, CHU Sart-Tilmant, Liege, Belgium
Cite this Article
Boniver, V., Moreau, P., & Lefebvre, P. (2005). Synovial sarcoma of the larynx: case report and literature review. B-ENT, 1(1), 47–51. Retrieved from https://www.b-ent.be/index.php/pub/article/view/8
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