2B52 Ewing sarcoma, primary site

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


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.

sections/codes in this section (2B52-2B52)

postcoordination

Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.

Laterality  - only one may be selected
Specific anatomy  - multiple selections are allowed
Has manifestation  - multiple selections are allowed
Has severity  - only one may be selected
Has alternative severity2  - only one may be selected
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