Pleural Epithelioid Mesothelioma

Preferred Label : Pleural Epithelioid Mesothelioma;

NCIt definition : Malignant mesothelioma that arises from the pleura. It is characterized by the presence of cells with epithelioid morphology. The epithelioid cells usually have eosinophilic cytoplasm, bland nuclei, and form tubulopapillary, microglandular, or sheet-like patterns.;

Neoplastic status : Malignant;

Détails

Origin ID

C45662;

UMLS CUI

C1709574;

Disease may have findings
- Anorexia [NCIt concept]
- Chest Pain [NCIt concept]
- Chills [NCIt concept]
- Dyspnea [NCIt concept]
- Fatigue [NCIt concept]
- Malaise [NCIt concept]
- Microglandular Pattern [NCIt concept]
- Papillary Growth Pattern [NCIt concept]
- Pleural Effusion [NCIt concept]
- Sheet-Like Growth Pattern [NCIt concept]
- Sweating [NCIt concept]
- Tubular Pattern [NCIt concept]
- Weight Loss [NCIt concept]
Excludes anatomical site(s)
- Neck [NCIt concept]
Has associated anatomic sites
- Pleural Cavity [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Mesothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Mesothelial Cell [NCIt concept]
disease_has_finding
- Diffuse Pattern [NCIt concept]
- Epithelioid Differentiation [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Mesothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Mesothelium [NCIt concept]
- Pleura [NCIt concept]
disease_has_primary_anatomic_site
- Pleural Cavity [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 15q [NCIt concept]
- Gain of Chromosome 17q [NCIt concept]
- Gain of Chromosome 1q [NCIt concept]
- Gain of Chromosome 5p [NCIt concept]
- Gain of Chromosome 7p [NCIt concept]
- Gain of Chromosome 8q [NCIt concept]
- Loss of Chromosome 1 [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 17p [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- Loss of Chromosome 3 [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Loss of Chromosome 4q [NCIt concept]
- Loss of Chromosome 6q [NCIt concept]
- Loss of Chromosome 9 [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
- Monosomy 22 [NCIt concept]
disease_may_have_molecular_abnormality
- BAP1 Gene Mutation [NCIt concept]
- CDKN2A Gene Inactivation [NCIt concept]
- Inactivating GPC3 Gene Mutation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]
- NF2 Gene Mutation [NCIt concept]

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