Ewing Sarcoma of Bone

Preferred Label : Ewing Sarcoma of Bone;

NCIt synonyms : Ewing's Sarcoma, Osseous; Skeletal Ewing's Sarcoma; Osseous Ewing's Sarcoma; Bone Ewing's Sarcoma; Skeletal Ewing's Tumor; Ewing's Sarcoma of Bone; Osseous Ewing's Tumor; Ewing s Sarcoma of Bone;

NCIt definition : A small round cell bone 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, leukocytosis, 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.;

Neoplastic status : Malignant;

Détails

Origin ID

C4835;

UMLS CUI

C0585474;

Automatic exact mappings (from CISMeF team)
- Ewing sarcoma of bone [DO Concept]
- Ewing's sarcoma of bone (disorder) [SNOMED CT concept]
- Skeletal Ewing sarcoma [ORDO Disease]
DO Cross reference
- Ewing sarcoma of bone [DO Concept]
Disease excludes abnormal cell
- Malignant Epithelial Cell [NCIt concept]
Disease excludes normal cell origin
- Bone Marrow Stem Cell [NCIt concept]
- Epithelial Cell [NCIt concept]
Disease may have findings
- Fever [NCIt concept]
- Hemorrhagic Change [NCIt concept]
- Homer Wright Rosette Formation [NCIt concept]
- Necrotic Change [NCIt concept]
- Pain [NCIt concept]
Excludes anatomical site(s)
- Soft Tissue [NCIt concept]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective Tissue [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Has cytogenetic abnormalities
- EWSR1 Gene Rearrangement [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Ewing's sarcoma of bone (disorder) [SNOMED CT concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_excludes_cytogenetic_abnormality
- CIC Gene Rearrangement [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Intermediate Filaments Present [NCIt concept]
- Intracytoplasmic Eosinophilic Inclusion [NCIt concept]
- Neuroectodermal Differentiation [NCIt concept]
disease_excludes_molecular_abnormality
- EWSR1-NFATC2 Fusion Protein Expression [NCIt concept]
- EWSR1-PATZ1 Fusion Protein Expression [NCIt concept]
- FUS-NFATC2 Fusion Protein Expression [NCIt concept]
disease_excludes_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Primitive Round to Oval Cell [NCIt concept]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective Tissue [NCIt concept]
- Embryonic Tissue [NCIt concept]
- Neural Crest [NCIt concept]
disease_has_primary_anatomic_site
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
disease_mapped_to_gene
- EWSR1 Gene [NCIt concept]
- EWSR1/ERG Fusion Gene [NCIt concept]
- EWSR1/ETV1 Fusion Gene [NCIt concept]
- EWSR1/ETV4 Fusion Gene [NCIt concept]
- EWSR1/FEV Fusion Gene [NCIt concept]
- EWSR1/FLI1 Fusion Gene [NCIt concept]
- FUS/ERG Fusion Gene [NCIt concept]
disease_may_have_abnormal_cell
- Malignant Small Round Cell [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
disease_may_have_cytogenetic_abnormality
- inv(22q12) [NCIt concept]
- t(11;22)(q24;q12) [NCIt concept]
- t(16;21)(p11;q22) [NCIt concept]
- t(17;22)(q21;q12) [NCIt concept]
- t(1;22)(p36.1;q12) [NCIt concept]
- t(21;22)(q22;q12) [NCIt concept]
- t(2;22)(q33;q12) [NCIt concept]
- t(7;22)(p22;q12) [NCIt concept]
disease_may_have_molecular_abnormality
- EWSR1-ERG Fusion Protein Expression [NCIt concept]
- EWSR1-ETV1 Fusion Protein Expression [NCIt concept]
- EWSR1-ETV4 Fusion Protein Expression [NCIt concept]
- EWSR1-FEV Fusion Protein Expression [NCIt concept]
- EWSR1-FLI1 Fusion Protein Expression [NCIt concept]
- FUS-ERG Fusion Protein Expression [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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