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Journal of Case Reports in Medicine,2013,2,1,1-3.Published:April 2013Type:Case ReportAuthors:Jaime Eaglin Moore, Amanda Hu, and Robert T. Sataloff Author(s) affiliations:Jaime Eaglin Moore, Amanda Hu, and Robert T. Sataloff Department of Otolaryngology – Head and Neck Surgery, College of Medicine, Drexel University, 1721 Pine St., Philadelphia, PA 19103, USA. Abstract:Introduction. To our knowledge, there is only one other reported case of arytenoid chondroma (1956). Our case report highlights the diagnosis and management of this rare disorder. Case report. A 33-year-old woman presented with a two-month history of episodic severe dysphonia and shortness of breath. On examination, she had left arytenoid fullness and left vocal fold hypomobility. A magnetic resonance imaging (MRI) of the neck with and without gadolinium showed a mass arising from the left arytenoid with soft tissue swelling. She underwent micro-direct laryngoscopy with excisional biopsy of the cartilaginous mass revealin
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Journal of Case Reports in Medicine,2013,2,1,1-3.Published:April 2013Type:Case ReportAuthors:Jaime Eaglin Moore, Amanda Hu, and Robert T. Sataloff Author(s) affiliations:Jaime Eaglin Moore, Amanda Hu, and Robert T. Sataloff Department of Otolaryngology – Head and Neck Surgery, College of Medicine, Drexel University, 1721 Pine St., Philadelphia, PA 19103, USA. Abstract:Introduction. To our knowledge, there is only one other reported case of arytenoid chondroma (1956). Our case report highlights the diagnosis and management of this rare disorder. Case report. A 33-year-old woman presented with a two-month history of episodic severe dysphonia and shortness of breath. On examination, she had left arytenoid fullness and left vocal fold hypomobility. A magnetic resonance imaging (MRI) of the neck with and without gadolinium showed a mass arising from the left arytenoid with soft tissue swelling. She underwent micro-direct laryngoscopy with excisional biopsy of the cartilaginous mass revealin
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