Small Cell Undifferentiated Hepatoblastoma

Preferred Label : Small Cell Undifferentiated Hepatoblastoma;

NCIt synonyms : SCUD HBL;

NCIt definition : A hepatoblastoma composed exclusively of noncohesive sheets of small undifferentiated cells. Cases showing loss of INI1 nuclear staining should be classified as rhabdoid tumors.;

Alternative definition : NICHD: A hepatoblastoma exclusively comprising noncohesive sheets of small undifferentiated cells.;

Neoplastic status : Malignant;

Details

Origin ID

C7096;

UMLS CUI

C1335981;

Disease excludes abnormal cell
- Small Cuboidal Cell Resembling Fetal Hepatocyte [NCIt concept]
Disease may have findings
- Abdominal Mass [NCIt concept]
- Anorexia [NCIt concept]
- Diaphragmatic Hernia [NCIt concept]
- Jaundice [NCIt concept]
- Meckel Diverticulum [NCIt concept]
- Thrombocytosis [NCIt concept]
- Weight Loss [NCIt concept]
Excludes anatomical site(s)
- Extrahepatic Bile Duct [NCIt concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Mesenchymal Component Present [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Small Round Cell with Scant Amount of Dark Granular Cytoplasm [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]
disease_mapped_to_gene
- CTNNB1 Gene [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
- Inguinal Hernia [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 11p [NCIt concept]
- Trisomy 2 [NCIt concept]
- Trisomy 20 [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]
- NFE2L2 Gene Mutation [NCIt concept]
- TERT Promoter Mutation [NCIt concept]

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