Ewing sarcoma, primary site (Q38773): Difference between revisions
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| description / pt-br | description / pt-br | ||
Tumor de pequenas células redondas em que falta evidência morfológica, imunohistoquímica e à microscopia eletrônica de diferenciação neuroectodérmica. Ele representa uma das duas extremidades do espectro chamado sarcoma de Ewing/tumor neuroectodérmico periférico. Afeta majoritariamente homens abaixo de 20 anos de idade, e pode ocorrer em tecidos moles ou osso. Dor e a presença de uma massa são os sintomas clínicos mais frequentes. | |||
| description / en | description / en | ||
A small round cell tumour that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing's sarcoma/peripheral neuroectodermal tumour. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms. | |||
Revision as of 03:58, 13 August 2026
A small round cell tumour that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing's sarcoma/peripheral neuroectodermal tumour. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 2B52 |
||
| English | Ewing sarcoma, primary site |
A small round cell tumour that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing's sarcoma/peripheral neuroectodermal tumour. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms. |
