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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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November 19, 2020
  • Description
  • Legends
  • Diagnosis
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Chondrosarcoma of the Cricoid Cartilage

  • Background:
    • Chondrosarcoma is a malignant tumor that shows extensive cartilage formation.
    • It accounts for 1% of laryngeal cancers, with 80% originating from cricoid cartilage.
    • The mean age at diagnosis is between 60 and 70 years, with a 3:1 male to female ratio.
    • It is classified into 3 histologic grades based on cellularity, atypia, and pleomorphism. Most are detected in grades I and II, with a 5-year survival rate of 90%.
  • Clinical Presentation:
    • Generally presents as a slow and painless growth
    • Symptoms include dysphonia, chronic nonproductive cough, dyspnea, and stridor, which are thought to occur when more than 75% of the tracheal lumen is occluded.
  • Key Diagnostic Features:
    • CT shows a hypodense or hyperdense, ill-defined, lobulated lesion with ring and arc calcifications (chondroid matrix).
    • Fifteen percent of chondrosarcomas do not demonstrate matrix calcification.
    • CT shows little to no enhancement, while heterogeneous enhancement may be seen with MRI.
  • Differential Diagnoses:
    • Chondroma can be difficult to distinguish from low-grade chondrosarcoma radiographically. Size greater than 4 cm, cortical breach, and older age are more suggestive of a chondrosarcoma.
    • Osteosarcoma is an expansive lytic lesion often associated with a soft tissue with or without calcifications.
    • Amyloidosis appears as well-defined submucosal masses without bone destruction.
    • Tracheopathia osteochondroplasia typically presents with scalloped nodular calcified opacities in the submucosa.
    • Posttraumatic chondrometaplasia appears as a rounded and circumscribed mass without infiltration of the surrounding tissues.
    • Laryngeal cartilage metastases are extremely rare and show cartilage destruction and heterogeneous enhancement.
  • Treatment:
    • Due to its low frequency, no established treatment approach for laryngeal chondrosarcoma exists. The treatment of choice is usually surgical resection.

Suggested Reading

  1. Coca-Pelaz A, Rodrigo JP, Triantafyllou A, et al. Chondrosarcomas of the head and neck. Eur Arch Otorhinolaryngol 2014;271:2601–09
  2. Buda I, Hod R, Feinmesser R, et al. Chondrosarcoma of the larynx. Isr Med Assoc J 2012;14:681–84

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American Journal of Neuroradiology: 46 (6)
American Journal of Neuroradiology
Vol. 46, Issue 6
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