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Extraskeletal Ewing's sarcoma of primary cardiac origin

✍ Scribed by J. C. Higgins; P. J. Katzman; S. B. Yeager; J. D. Dickerman; B. J. Leavitt; M. D. Tischler; R. W. Battle

Publisher
Springer
Year
1994
Tongue
English
Weight
374 KB
Volume
15
Category
Article
ISSN
0172-0643

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πŸ“œ SIMILAR VOLUMES

Extraskeletal Ewing's sarcoma
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✍ Rick Ahmad; Brian R. Mayol; Mary Davis; Bruce T. Rougraff πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 103 KB

## Background: Ewing's sarcoma usually is identified as a primary malignancy of bone affecting children and young adults. extraskeletal ewing's sarcoma is rare, and very few data are available addressing optimal surgical and oncologic treatment modalities. ## Methods: The authors chose to review

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## BACKGROUND. Extraskeletal Ewing sarcoma (EES) shares histologic, immunohistochemical, and molecular findings with ES of bone. The authors' goal in conducting this study was to examine the cytomorphologic features of EES. In addition, immunocytostaining for CD99/O13 was performed in all cases, a

Ewing sarcoma: Phalangeal primary with f
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✍ Wilson, Kenneth S. ;Nyssen, John ;Alexander, Skaria πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 English βš– 213 KB

## Abstract A 39‐year‐old man had pain and swelling of the terminal phalanx of a finger. Radiograph was interpreted as osteomyelitis, and amputation through the midphalanx was performed. Histology revealed Ewing sarcoma. Lung metastases rapidly developed. Right lung irradiation and systemic chemoth