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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Case of the Week

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada

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Submit a Case Previous Cases ASPNR Pediatric Cases

November 10, 2014
  • Description
  • Legends
  • Diagnosis
  • Brain Teaser
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Thyroid Cartilage Chondrosarcoma

  • An uncommon malignant neoplasm of cartilage, laryngeal chondrosarcoma represents less than 0.2% of head and neck malignancies, and 1% of laryngeal tumors. Head and neck cartilage distribution: 72% cricoid, 20% thyroid, and rarely, arytenoid.
  • Slow-growing, low-grade neoplasm (unless poorly differentiated subtype).
  • Clinical Presentation: Mean age: 4th to 6th decade, 5–10 times male predominance. Presents with slowly worsening hoarseness and dyspnea. Occasionally seen with dysphagia and a palpable neck mass. Referred otalgia can be seen.
  • Key Diagnostic Features:
    • CT is the preferred imaging modality, demonstrating a calcified mass involving laryngeal or tracheal cartilage.
    • Tumor matrix can demonstrate fine, punctate, stippled-to-coarse calcifications (popcorn and/or ring appearance).
    • Moderate postcontrast enhancement of the soft-tissue component.
    • MRI may improve delineation of soft-tissue involvement.
    • Pathologic grade I–III (higher grade correlates to poor differentiation and worse prognosis).
  • DDx:
    • Chondroma
    • Other sarcoma types
  • Rx: Surgery. Chemotherapy and radiotherapy have a limited role to play.

Suggested Reading

Sakai O, Curtin HD, Faquin WC, et al. Dedifferentiated chondrosarcoma of the larynx. AJNR Am J Neuroradiol 2000;21:584–86

Chen RC, Khorsandi AS, Shatzkes DR, et al. The radiology of referred otalgia. AJNR Am J Neuroradiol 2009;30:1817–23, 10.3174/ajnr.A1605

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