Conjunctival Melanoma In Situ

Preferred Label : Conjunctival Melanoma In Situ;

NCIt definition : A term that refers to conjunctival melanocytic intraepithelial lesions with severe atypia involving close to full thickness of the epithelium or lesions with histologic characteristics of melanoma that lack documented evidence of subepithelial invasion.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1927453;

Details

Origin ID

C204981;

Disease may have findings
- HMB-45-Positive Neoplastic Cells Present [NCIt concept]
- S-100-Positive Neoplastic Cells Present [NCIt concept]
Excludes anatomical site(s)
- Skin [NCIt concept]
Has associated anatomic sites
- Adnexa [NCIt concept]
- Conjunctiva [NCIt concept]
- Eye [NCIt concept]
- Head and Neck [NCIt concept]
- Ocular Adnexa [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Mild Cytologic Atypia [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Melanoma Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Melanocyte [NCIt concept]
disease_has_finding
- Cytologic Atypia [NCIt concept]
- High Grade Lesion [NCIt concept]
- In Situ Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Non-Invasive Lesion [NCIt concept]
disease_has_grade
- High Grade [NCIt concept]
disease_has_normal_cell_origin
- Melanocyte [NCIt concept]
disease_has_normal_tissue_origin
- Conjunctival Epithelium [NCIt concept]
disease_has_primary_anatomic_site
- Conjunctiva [NCIt concept]
- Eye [NCIt concept]
disease_may_have_molecular_abnormality
- BRAF NP_004324.2:p.V600X [NCIt concept]
- KIT Gene Mutation [NCIt concept]
- NF1 Gene Mutation [NCIt concept]
- NRAS Gene Mutation [NCIt concept]
- TERT Gene Mutation [NCIt concept]

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