Lung Hyalinizing Clear Cell Carcinoma

Preferred Label : Lung Hyalinizing Clear Cell Carcinoma;

NCIt definition : An extremely rare, low-grade carcinoma that arises endobronchially in the central airways. It is composed of small to medium-sized malignant epithelial cells with clear and eosinophilic cytoplasm forming nests, cords, and trabeculae in a hyalinized stroma. It is associated with the presence of EWSR1-ATF1 fusion gene.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1771462;

Details

Origin ID

C183116;

UMLS CUI

C5668153;

Disease excludes abnormal cell
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Excludes anatomical site(s)
- Neck [NCIt concept]
Has associated anatomic sites
- Lung [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Premalignant Lesion [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Cell with Eosinophilic Cytoplasm [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Malignant Epithelial Clear Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Hyalinized Stroma Formation [NCIt concept]
- Low Grade Lesion [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
- Lung [NCIt concept]
disease_mapped_to_gene
- EWSR1/ATF1 Fusion Gene [NCIt concept]
- TP53 Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- EWSR1 Gene Rearrangement [NCIt concept]

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