About: Ewing Sarcoma of Bone     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Ewing Sarcoma of Bone
equivalentClass
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Ewing Sarcoma of Bone
UMLS_CUI
  • C0585474
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Ewing_s_Sarcoma_of_Bone
FULL_SYN
  • Skeletal Ewing's TumorSYNCI
  • Ewing's Sarcoma of BoneSYNCI
  • Osseous Ewing's SarcomaSYNCI
  • Ewing's Sarcoma, OsseousSYNCI
  • Skeletal Ewing's SarcomaSYNCI
  • Bone Ewing's SarcomaSYNCI
  • Ewing Sarcoma of BonePTNCI
  • Osseous Ewing's TumorSYNCI
DEFINITION
  • A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It often affects the diaphysis or metaphyseal-diaphyseal portion of long bones. Clinical findings include pain and a mass in the involved area. Fever, anemia, leucocytosis, and an increased sedimentation rate are often seen. X-ray examination reveals osteolytic lesions. The prognosis depends on the stage, anatomic location, and size of the tumor. -- 2003NCI
code
  • C4835
is rdf:first of
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