Ewing sarcoma, primary site (Q38773): Difference between revisions

@@ 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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1651102476
@@ Property / Canonical URI: https://id.who.int/icd/entity/1651102476 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:2B52
@@ Property / CURIE: CID11:2B52 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-2B52
@@ Property / Canary Token: dki-india-2B52 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+C41.9
@@ Property / Linked ICD 10: C41.9 / rank @@
+Normal rank

Latest 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.