Solid Cystic Hidradenoma

Preferred Label : Solid Cystic Hidradenoma;

NCIt synonyms : Solid and Cystic Hidradenoma; SCH;

NCIt definition : A hidradenoma characterized by the presence of solid lobular neoplastic cell proliferations and cystic spaces filled with homogeneous eosinophilic material.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL608351;

Détails

Origin ID

C205539;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [NCIt concept]
Disease may have findings
- Apocrine Differentiation [NCIt concept]
- Eccrine Differentiation [NCIt concept]
Has associated anatomic sites
- Adnexa [NCIt concept]
- Integumentary System [NCIt concept]
- Skin [NCIt concept]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Dysplasia [NCIt concept]
- Invasive Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
disease_has_finding
- Adnexal Differentiation [NCIt concept]
- Benign Cellular Infiltrate [NCIt concept]
- Cutaneous Involvement [NCIt concept]
- Cystic Change [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Solid Growth Pattern [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Glandular Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Exocrine System [NCIt concept]
- Skin [NCIt concept]
- Skin Adnexa [NCIt concept]
- Sweat Gland [NCIt concept]
disease_mapped_to_gene
- CRTC1/MAML2 Fusion Gene [NCIt concept]
- CRTC3/MAML2 Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(11;19)(q21;p13) [NCIt concept]
disease_may_have_molecular_abnormality
- CRTC1-MAML2 Fusion Protein Expression [NCIt concept]
- CRTC3-MAML2 Fusion Protein Expression [NCIt concept]

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