Peritoneal Epithelioid Mesothelioma

Preferred Label : Peritoneal Epithelioid Mesothelioma;

NCIt definition : Malignant mesothelioma that arises from the peritoneum. 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;

NCI Metathesaurus CUI : CL973298;

Details

Origin ID

C162940;

UMLS CUI

C5206866;

Disease may have findings
- Abdominal Pain [NCIt concept]
- Microglandular Pattern [NCIt concept]
- Papillary Growth Pattern [NCIt concept]
- Peritoneal Effusion [NCIt concept]
- Sheet-Like Growth Pattern [NCIt concept]
- Tubular Pattern [NCIt concept]
Has associated anatomic sites
- Peritoneal Cavity [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP 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]
- Peritoneum [NCIt concept]
disease_has_primary_anatomic_site
- Peritoneal Cavity [NCIt concept]
disease_may_have_cytogenetic_abnormality
- 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 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Loss of Chromosome 4q [NCIt concept]
- Loss of Chromosome 6q [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
disease_may_have_molecular_abnormality
- BAP1 Gene Mutation [NCIt concept]
- CDKN2A Gene Inactivation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]

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