Peritoneal Sarcomatoid Mesothelioma

Preferred Label : Peritoneal Sarcomatoid Mesothelioma;

NCIt definition : Malignant mesothelioma that arises from the peritoneum. It is characterized by the presence of spindle cells. Anaplastic morphologic features and multinucleated malignant cells may also be seen.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1378702;

Details

Origin ID

C168804;

UMLS CUI

C5239129;

Disease may have findings
- Abdominal Pain [NCIt concept]
- Anaplastic Lesion [NCIt concept]
- Peritoneal Effusion [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]
- Malignant Spindle Mesothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Mesothelial Cell [NCIt concept]
disease_has_finding
- Diffuse Pattern [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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