2014
DOI: 10.1016/j.bjorl.2014.05.004
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Laryngeal chondrosarcoma – Ten years of experience

Abstract: Laryngeal chondrosarcomas remain a rare disease of unknown etiology, with slow and insidious symptoms. The treatment is surgical, with favorable prognosis, and metastases rarely occur. The main concern regards their propensity to relapse.

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Cited by 32 publications
(51 citation statements)
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“…The primary site was most commonly the cricoid in 75% of cases, followed by the thyroid cartilage in 20%, and epiglottis or arytenoids in 5% [1]. Laryngeal chondrosarcomas appear around the age of 60 to 70 years with a clear predominance in males [1][2][3][4][5], as in our patient.…”
Section: Discussionmentioning
confidence: 60%
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“…The primary site was most commonly the cricoid in 75% of cases, followed by the thyroid cartilage in 20%, and epiglottis or arytenoids in 5% [1]. Laryngeal chondrosarcomas appear around the age of 60 to 70 years with a clear predominance in males [1][2][3][4][5], as in our patient.…”
Section: Discussionmentioning
confidence: 60%
“…It accounts for 0.07 to 2% of laryngeal cancers and less than 1% of all sarcomas [1][2][3][4]. The primary site was most commonly the cricoid in 75% of cases, followed by the thyroid cartilage in 20%, and epiglottis or arytenoids in 5% [1].…”
Section: Discussionmentioning
confidence: 99%
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