Primární Ewingův sarkom v retroperitoneu

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Autoři: 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
Působiště autorů: 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
Vyšlo v časopise: Rozhl. Chir., 2019, roč. 98, č. 3, s. 121-124.
Kategorie: case report

Souhrn

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

Zdroje

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