ORPHA:213605
Carcinofibroma of the corpus uteri
- Type
- Disease
- Group
- Disorder
- Status
- active
Carcinofibroma of the corpus uteri is an extremely rare subtype of mixed müllerian tumor characterized by the presence of a uterine neoplasm which simuntaneously presents a malignant epithelial component (carcinomatous glands) and a benign mesenchymal component. Clinical presentation typically includes dysfunctional vaginal bleeding, abnormal vaginal discharge and/or lower abdominal pain.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Carcinofibroma of the corpus uteri | |
| fr | Carcinofibrome du corps de l'utérus | |
| de | Karzinofibrom des Corpus uteri | |
| es | Carcinofibroma de cuerpo de útero | |
| it | Carcinofibroma del corpo dell'utero | |
| nl | Carcinofibroom van corpus uteri | Carcinofibroom van baarmoederlichaam |
| pt | Carcinofibroma do corpo uterino | |
| pl | Włókniakorak trzonu macicy | |
| cs | Karcinofibrom těla děložního | |
| uk | Карцинофіброма тіла матки | |
| zh | 子宫体癌纤维瘤 | |
| tr | Korpus uteri karsinofibromu |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C54.0 | BTNT | attributed | validated |
| ICD-10 | C54.1 | BTNT | attributed | validated |
| ICD-10 | C54.2 | BTNT | attributed | validated |
| ICD-10 | C54.3 | BTNT | attributed | validated |
| ICD-10 | C54.8 | BTNT | attributed | validated |
| ICD-11 | 2B5D.1 | NTBT | index | validated |
| MONDO | 0016258 | E | validated | |
| UMLS | C4755313 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:213589Malignant mixed epithelial and mesenchymal tumor of corpus uteri
rare neoplastic diseases; rare gynecological and obstetric diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/213605
- This record as JSON: /data/d/213605.json