Rapidly growing intrathoracic extraskeletal Ewing's sarcoma

Interact Cardiovasc Thorac Surg. 2012 Jan;14(1):117-9. doi: 10.1093/icvts/ivr023. Epub 2011 Nov 15.

Abstract

There are few reported cases of intrathoracic Ewing's sarcoma, a very rare malignant neoplasm. We report a surgical case of extraskeletal Ewing's sarcoma that had been followed-up as a stable sized tumour for many years, which then grew rapidly within a year. A 27-year old female patient with a rapidly growing abnormal shadow on chest roentgenogram was admitted to our department. She had undergone periodic examinations including chest computed tomography (CT) scans for 6 years since a small nodule in her chest had been pointed out by chest roentgenogram. The initial CT demonstrated a solitary nodule with a diameter of 20 mm on the parietal pleura that covered the V rib of the posterior chest wall. For 5 years the tumour's size did not change noticeably but it suddenly grew to about 90 mm diameter in a year. The tumour volume doubling time was calculated to be 17 days.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Humans
  • Magnetic Resonance Imaging
  • Neoplasm Staging
  • Pneumonectomy
  • Positron-Emission Tomography
  • Sarcoma, Ewing / diagnosis*
  • Sarcoma, Ewing / surgery
  • Thoracic Neoplasms / diagnosis*
  • Thoracic Neoplasms / surgery
  • Thoracoscopy / methods*
  • Time Factors
  • Tomography, X-Ray Computed