Journal of the Egyptian National Cancer Institute (Dec 2018)

Laryngeal synovial sarcoma: Report of 2 cases

  • Mouna Bellakhdhar,
  • Amira Cheniti,
  • Monia Ghammem,
  • Ahlem Bdioui,
  • Sarra Mestiri,
  • Abir Meherzi,
  • Wassim Kermani,
  • Mohamed Abdelkefi

Journal volume & issue
Vol. 30, no. 4
pp. 173 – 176

Abstract

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Synovial sarcoma is a malignant mesenchymal tumor. It most commonly occurs in the lower extremities of young adults. The head and neck are rare sites, accounting for less than 10%. The larynx is an extremely rare site.We report two cases of 27 and 18 year-old men who developed a synovial sarcoma of the larynx. They presented with hoarseness of voice and hemoptysis. Endoscopy detected a mass in the supraglottic region. The biopsy concluded a synovial sarcoma. Immunohistochemistry conveyed diagnostic certainty. They had been treated with total laryngectomy and post-operative radiotherapy. The 2 patients are seen for regular follow-ups in our department and they remained recurrence-free for 10 years and 24 months, respectively.Synovial sarcoma is a very rare tumor of the larynx. A multidisciplinary therapeutic approach is essential for the management of this malignancy. Long-term follow-up is required to monitor for recurrence and improve disease-free survival. Keywords: Synovial sarcoma, Larynx, Head and neck