Laryngeal Pleomorphic Adenoma

Preferred Label : Laryngeal Pleomorphic Adenoma;

NCIt definition : A very rare pleomorphic adenoma that arises from the larynx.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL1407229;

Details

Origin ID

C173412;

UMLS CUI

C5420197;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease may have findings
- Cartilaginous Component Present [NCIt concept]
- Encapsulated Mass [NCIt concept]
- Lipomatous Component Present [NCIt concept]
- Myxoid Stroma Formation [NCIt concept]
- Osseous Component Present [NCIt concept]
- Slow Growing Painless Mass [NCIt concept]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Larynx [NCIt concept]
- Neck [NCIt concept]
- Salivary Gland [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_cytogenetic_abnormality
- Loss of Chromosome 11q [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 16q [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
- Loss of Chromosome 9q [NCIt concept]
disease_excludes_finding
- Carcinomatous Component Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Malignant Epithelial Cell Population [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Mesenchymal Component Present [NCIt concept]
- Mixed Cellular Population [NCIt concept]
disease_has_normal_cell_origin
- Cell [NCIt concept]
- Epithelial Cell [NCIt concept]
- Myoepithelial Cell [NCIt concept]
- Salivary Gland Myoepithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Head and Neck [NCIt concept]
- Larynx [NCIt concept]
- Neck [NCIt concept]
- Salivary Gland [NCIt concept]
disease_mapped_to_gene
- CTNNB1/PLAG1 Fusion Gene [NCIt concept]
- HMGA2 Gene [NCIt concept]
- PLAG1 Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(3;8)(p12;q21) [NCIt concept]

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