Orbital Inflammatory Myofibroblastic Tumor

Preferred Label : Orbital Inflammatory Myofibroblastic Tumor;

NCIt definition : An intermediate fibroblastic neoplasm that arises from the orbit and is characterized by the presence of spindle-shaped fibroblasts and myofibroblasts, and a chronic inflammatory infiltrate composed of eosinophils, lymphocytes, and plasma cells.;

Neoplastic status : Undetermined;

Détails

Origin ID

C217094;

Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Fascicular Pattern [NCIt concept]
- Fever [NCIt concept]
- Multinodular Lesion [NCIt concept]
- Myxoid Changes Present [NCIt concept]
- Pain [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
Excludes anatomical site(s)
- Maxillofacial Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Head and Neck [NCIt concept]
- Orbit [NCIt concept]
- Soft Tissue [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Fibroblast [NCIt concept]
- Neoplastic Spindle-Shaped Fibroblast [NCIt concept]
- Neoplastic Spindle-Shaped Myofibroblast [NCIt concept]
disease_has_finding
- Eosinophilic Infiltrate [NCIt concept]
- Locally Aggressive Lesion [NCIt concept]
- Lymphocytic Infiltrate [NCIt concept]
- Plasmacytic Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Fibroblast [NCIt concept]
disease_has_primary_anatomic_site
- Connective and Soft Tissue [NCIt concept]
- Head and Neck [NCIt concept]
- Orbit [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- ALK Gene [NCIt concept]
- CLTC/ALK Fusion Gene [NCIt concept]
- HMGA2 Gene [NCIt concept]
- TPM3/ALK Fusion Gene [NCIt concept]
- TPM4/ALK Fusion Gene [NCIt concept]
disease_may_have_abnormal_cell
- Ganglion-Like Cell [NCIt concept]
- Neoplastic Stellate Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(1;2)(q25;p23) [NCIt concept]
- t(2;17)(p23;q23) [NCIt concept]
- t(2;19)(p23;p13) [NCIt concept]
disease_may_have_molecular_abnormality
- ALK Gene Rearrangement [NCIt concept]
- CLTC-ALK Fusion Protein Expression [NCIt concept]
- TPM3-ALK Fusion Protein Expression [NCIt concept]
- TPM4-ALK Fusion Protein Expression [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients