Lacrimal Gland Warthin Tumor

Preferred Label : Lacrimal Gland Warthin Tumor;

NCIt definition : A rare benign tumor that arises from the lacrimal gland and is characterized by the presence of an oncocytic epithelial component and dense lymphoid stroma.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL1412771;

Details

Origin ID

C175291;

UMLS CUI

C5446411;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [NCIt concept]
Disease may have findings
- Lipogranuloma [NCIt concept]
- Lymphoplasmacytic Infiltrate [NCIt concept]
- Painless Mass [NCIt concept]
- Reactive Germinal Centers Present [NCIt concept]
Excludes anatomical site(s)
- Lymphatic System [NCIt concept]
Has associated anatomic sites
- Adnexa [NCIt concept]
- Eye [NCIt concept]
- Head and Neck [NCIt concept]
- Lacrimal Apparatus [NCIt concept]
- Lacrimal Gland [NCIt concept]
- Ocular Adnexa [NCIt concept]
- Salivary Gland [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Oncocyte [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Cystic Change [NCIt concept]
- Encapsulated Mass [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Lymphocytic Infiltrate [NCIt concept]
- Papillary Growth Pattern [NCIt concept]
- Squamous Metaplasia [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]
- Head and Neck [NCIt concept]
- Lacrimal Apparatus [NCIt concept]
- Lacrimal Gland [NCIt concept]
- Ocular Adnexa [NCIt concept]
- Salivary Gland [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(11;19)(q21;p13) [NCIt concept]

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