Gallbladder Hepatoid Adenocarcinoma

Preferred Label : Gallbladder Hepatoid Adenocarcinoma;

NCIt definition : A rare variant of gallbladder adenocarcinoma. It is characterized by the presence of a malignant glandular epithelial infiltrate that resembles hepatocellular carcinoma.;

Neoplastic status : Malignant;

Details

Origin ID

C96890;

UMLS CUI

C2030691;

Disease excludes abnormal cell
- Malignant Squamous Cell [NCIt concept]
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
Disease may have findings
- Abdominal Pain [NCIt concept]
Excludes anatomical site(s)
- Liver [NCIt concept]
Has associated anatomic sites
- Biliary Tract [NCIt concept]
- Digestive System [NCIt concept]
- Gallbladder [NCIt concept]
- Hepatobiliary System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Intermediate Grade Neuroendocrine Lesion [NCIt concept]
- Low Grade Neuroendocrine Lesion [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
- Well Differentiated Neuroendocrine Lesion [NCIt concept]
disease_has_abnormal_cell
- Adenocarcinoma Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
- Polygonal Adenocarcinoma Cell with Eosinophilic Cytoplasm [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Glandular Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Gallbladder Epithelium [NCIt concept]
disease_has_primary_anatomic_site
- Biliary Tract [NCIt concept]
- Digestive System [NCIt concept]
- Gallbladder [NCIt concept]
- Pancreatobiliary System [NCIt concept]
disease_mapped_to_gene
- CDKN2A Gene [NCIt concept]
- ERBB2 Gene [NCIt concept]
- KRAS Gene [NCIt concept]
- TP53 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- CDKN2A Gene Inactivation [NCIt concept]
- ERBB2 Gene Amplification [NCIt concept]
- KRAS Gene Mutation [NCIt concept]
- TP53 Gene Inactivation [NCIt concept]

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