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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
E E0 E6 E7 EA EB EC ED EE EF EG EH EI EJ EK EL EM EN EO EP EQ ER ES ET EU EV EW EX EY
EXA EXC EXE EXF EXH EXI EXL EXO EXP EXS EXT EXU EXV

Extraosseous Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor

[A spectrum of malignant tumors arising from the soft tissues, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. Pain and the presence of a mass are the most common clinical symptoms. — 2004 ( NCI )]
UMLS (NCI) C1333514
Extraosseous Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor
 
Neoplastic Process

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