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Primární Ewingův sarkom v retroperitoneu


Authors: J. Spacek 1;  K. Kopeckova 2;  J. Kosina 1;  J. Pacovsky 1;  J. Petera 3;  L. Krbal 4;  M. Mrhalová 5;  P. Dvorak 6;  M. Broďák 1
Authors‘ workplace: Department of Urology, Faculty of Medicine in Hradec Kralove and University Hospital, Hradec Kralove 1;  Department of Oncology, 2nd Faculty of Medicine and Faculty Hospital Motol, Charles University, Prague 2;  Department of Oncology and Radiotherapy, Faculty of Medicine in Hradec Kralove and University Hospital, Hradec Kralove 3;  The Fingerland Department of Pathology, Faculty of Medicine in Hradec Kralove and University Hospital, Hradec Kralove 4;  Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine and Faculty Hospital Motol, Charles University, Prague 5;  Department of Radiology, Faculty of Medicine in Hradec Kralove and University Hospital, Hradec Kralove 6
Published in: Rozhl. Chir., 2019, roč. 98, č. 3, s. 121-124.
Category:

Overview

Rodina Ewingových sarkomů (EWS) jsou tumory z malých kulatých buněk s různým stupněm neuroektodermální diferenciace. Jedná se o tumory mezenchymálního původu, které se vyskytují i u dětí a mladých dospělých. Nejčastěji jsou postižené dlouhé kosti končetin, asi 10–20 % má primární extraskeletální lokalizaci.

Klíčová slova:

Ewingův sarkom – retroperitoneum – počítačová tomografie – lumbotomie


Sources
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Perspectives in Surgery

Issue 3

2019 Issue 3

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