Literature DB >> 22108933

Rapidly growing intrathoracic extraskeletal Ewing's sarcoma.

Yoshio Tsunezuka1, Takahiro Furusawa, Tsuyoshi Yachi, Hiroshi Kurumaya.   

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.

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Year:  2011        PMID: 22108933      PMCID: PMC3420268          DOI: 10.1093/icvts/ivr023

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  6 in total

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Journal:  Ann Thorac Surg       Date:  2006-04       Impact factor: 4.330

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Journal:  Cancer       Date:  1975-08       Impact factor: 6.860

  6 in total
  1 in total

1.  Atypical growth on MRI in a case of Ewing's sarcoma despite lower SUV on PET.

Authors:  Zachary Sanford; Stanford Israelsen; Rajesh Sehgal; Felix H Cheung
Journal:  Skeletal Radiol       Date:  2013-12-19       Impact factor: 2.199

  1 in total

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