Phyllodes tumor of the breast
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult
- Status
- active
A rare fibroepithelial tumor of the breast characterized by a painless, circumscribed, firm mass potentially arising in any part of the breast, histologically showing a prominent intracanalicular growth pattern with leaf-like stromal fronds, capped by luminal epithelial and myoepithelial cell layers, accompanied by stromal hypercellularity. The tumor may be benign, borderline, or malignant.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Phyllodes tumor of the breast | |
| fr | Tumeur phyllode du sein | Tumeur phylloïde du sein |
| de | Phylloidestumor der Brust | |
| es | Tumor filoide de la mama | |
| it | Tumore filloide della mammella | |
| nl | Phyllodestumor van borst | |
| pt | Tumor filóide da mama | |
| pl | Guz liściasty gruczołu piersiowego | Guz liściasty |
| cs | Fyloidní tumor prsu | Cystosarcoma phyllodes |
| uk | Філлодна пухлина молочної залози | |
| zh | 乳房叶状肿瘤 | 乳房叶状囊性肉瘤 |
| tr | Memenin filloid tümörü | Memenin sistosarkom filodları |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D48.6 | NTBT | inclusion | validated |
| ICD-11 | 2F30.3 | E | specific | validated |
| MONDO | 15871 | E | validated | |
| MeSH | D003557 | E | validated | |
| UMLS | C0238031 | E | validated | |
| GARD | 9514 | E | validated | |
| MedDRA | 10011813 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:180253Rare benign breast tumor
rare neoplastic diseases; rare gynecological and obstetric diseases - ORPHA:180257Rare malignant breast tumor
rare neoplastic diseases; rare gynecological and obstetric diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180261
- This record as JSON: /data/d/180261.json