CASE REPORT Sternal Chondrosarcoma After Sternotomy for Coronary Artery Bypass Grafting

Vijay A Singh1, Juan Abreu, Kimberly Bowman

  • 1Cardiothoracic Surgery Department.

Eplasty
|February 2, 2013
PubMed

Insights

A rare sternal chondrosarcoma developed in a patient 4 years after cardiac surgery. Wide surgical excision is crucial for potentially curing these uncommon primary sternal sarcomas.

Area of Science:

  • Oncology
  • Surgical Pathology
  • Cardiothoracic Surgery

Background:

  • Primary bony tumors of the chest wall are typically benign, with ribs and sternum being common sites.
  • Sternal chondrosarcoma is a rare primary malignancy of the chest wall.
  • Post-sternotomy chondrosarcoma is exceptionally rare.

Purpose of the Study:

  • To present a rare case of sternal chondrosarcoma.
  • To highlight the diagnostic and therapeutic challenges of post-sternotomy sternal tumors.

Main Methods:

  • A patient presented with a rapidly enlarging sternal mass 4 years post-coronary artery bypass grafting.
  • Diagnostic imaging included computed tomographic (CT) scan and magnetic resonance imaging (MRI).
  • Surgical excision of the sternal mass was performed.

Main Results:

  • Imaging revealed an 8.4 × 6.2 × 8.6 cm complex solid mass originating from the sternal manubrium with extensive bone destruction.
  • Biopsy results were initially inconclusive (cells of uncertain significance).
  • Histopathological diagnosis confirmed a grade II chondrosarcoma.

Conclusions:

  • Primary sternal sarcomas, though uncommon, are potentially curable with adequate surgical resection.
  • Treatment success and recurrence risk are dependent on tumor histology and grade.
Abstract

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