Epithelioid trophoblastic tumor
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare gestational trophoblastic neoplasmcharacterized histologically by invasion of the myometrium and/or cervix uteri by regular epithelioid cells of chorion laeve type intermediate trophoblasts which clusters in a hyaline stroma. The disease generally occurs several years after pregnancy and indicative signs are irregular metrorrhagia and moderate increases in chorionic gonadotropin levels.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Epithelioid trophoblastic tumor | |
| fr | Tumeur trophoblastique épithélioïde | |
| de | Trophoblasttumor, epitheloider | |
| es | Tumor trofoblástico epitelioide | |
| it | Tumore trofoblastico epitelioide | |
| nl | Epithelioïde trofoblasttumor | |
| pt | Tumor trofoblástico epitelióide | |
| pl | Epitelioidalny guz trofoblastyczny | |
| cs | Epiteloidní trofoblastický nádor | |
| uk | Епітеліоїдна трофобластична пухлина | |
| zh | 上皮样滋养层细胞肿瘤 | |
| tr | Epiteloid trofoblastik tümör |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C58 | NTBT | attributed | validated |
| ICD-11 | 2C75.0 | NTBT | index | validated |
| ICD-11 | XH8FW3 | E | specific | validated |
| MONDO | 0016787 | E | validated | |
| UMLS | C1266159 | 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 (1):
- ORPHA:59305Gestational trophoblastic neoplasm
rare neoplastic diseases; rare gynecological and obstetric diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Annual incidence | Unknown | — | Europe | Class only | Validated | ORPHANET |
| Lifetime Prevalence | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/254698
- This record as JSON: /data/d/254698.json