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Chondrosarcoma of the larynx
Inon Buda1, Roy Hod, Raphael Feinmesser
1Department of Otolaryngology-Head and Neck Surgery, Rabin Medical Center (Beilinson Campus), Petah Tikva, affiliated with Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel. inonb@clalit.org.il
Laryngeal chondrosarcoma, a rare tumor, often presents with hoarseness. Surgical treatment, such as laryngectomy, is recommended, with long-term follow-up advised for potential recurrence.
Area of Science:
- Otolaryngology
- Oncology
- Surgical Pathology
Background:
- Laryngeal chondrosarcoma is an exceptionally rare cartilaginous tumor.
- Hoarseness is the predominant presenting symptom.
- Optimal treatment strategies remain a subject of debate.
Purpose of the Study:
- To present a case series of six patients diagnosed with laryngeal chondrosarcoma.
- To review clinical data, treatment modalities, and patient outcomes from a single tertiary care center.
Main Methods:
- Retrospective review of medical records for patients diagnosed with laryngeal chondrosarcoma between 1959 and 2010.
- Data collection encompassed patient demographics, clinical presentation, surgical interventions, adjuvant therapies, and follow-up outcomes.
Main Results:
- Six male patients with a mean age of 53.3 years were identified.
- Surgical interventions included partial laryngectomy (3), total laryngectomy (1), local excision (1), and partial cricoidectomy (1).
- Four patients required permanent tracheostomy; one received chemotherapy and one radiotherapy. Recurrence occurred in two patients, successfully treated with salvage surgery. Long-term follow-up ranged from 12 to 216 months.
Conclusions:
- Findings support partial or total laryngectomy as the primary treatment for laryngeal chondrosarcoma.
- Emphasizes the necessity of long-term surveillance for tumor recurrence.
- Recommends laryngeal preservation when feasible, even if a permanent tracheostomy is required.
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