Lacrimal Gland Mucoepidermoid Carcinoma

Preferred Label : Lacrimal Gland Mucoepidermoid Carcinoma;

NCIt synonyms : Mucoepidermoid Carcinoma of Lacrimal Gland; Mucoepidermoid Carcinoma of the Lacrimal Gland;

NCIt definition : An extremely rare carcinoma that arises from the lacrimal gland. It is characterized by the presence of infiltrating nests of epidermoid cells and mucus producing cells.;

Neoplastic status : Malignant;

Details

Origin ID

C6091;

UMLS CUI

C1334359;

Currated CISMeF NLP mapping
- lacrimal gland mucoepidermoid carcinoma [DO Concept]
DO Cross reference
- lacrimal gland mucoepidermoid carcinoma [DO Concept]
Disease excludes abnormal cell
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease may have findings
- Globular Hyaline Body [NCIt concept]
Has associated anatomic sites
- Eye [NCIt concept]
- Lacrimal Apparatus [NCIt concept]
- Lacrimal Gland [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- lacrimal gland mucoepidermoid carcinoma [DO Concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Cuboidal Mucous Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Malignant Goblet-Like Mucous Cell [NCIt concept]
- Malignant Squamoid Cell [NCIt concept]
- Mucin-Producing Malignant Epithelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Cystic Change [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Fibrotic Stroma Formation [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Eye [NCIt concept]
- Lacrimal Apparatus [NCIt concept]
- Lacrimal Gland [NCIt concept]
disease_mapped_to_gene
- CRTC1/MAML2 Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(11;19)(q21;p13) [NCIt concept]
disease_may_have_molecular_abnormality
- CRTC1-MAML2 Fusion Protein Expression [NCIt concept]

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