raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213600

Adenosarcoma of the corpus uteri

Type
Disease
Group
Disorder
Status
active

A rare subtype of mixed epithelial-mesenchymal tumor, often presenting as a large, exophytic polypoid lesion, which may extend through the cervix, composed of benign or atypical epithelium and low-grade malignant stroma. It usually presents with dysfunctional bleeding or vaginal discharge and less often abdominal pain. Association with long-term unopposed estrogen therapy, tamoxifen therapy and a history of pelvic radiation has been reported.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAdenosarcoma of the corpus uteri
frAdénosarcome du corps de l'utérus
deAdenosarkom des Corpus uteri
esAdenosarcoma de cuerpo uterino
itAdenosarcoma del corpo dell'utero
nlAdenosarcoom van baarmoederlichaamAdenosarcoom van corpus uteri
ptAdenossarcoma do corpo uterino
plGruczolakomięsak trzonu macicy
csAdenosarkom těla děložního
ukАденосаркома тіла матки
zh子宫体腺肉瘤
trKorpus uteri adenosarkomu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C54.2BTNTattributedvalidated
ICD-112B5D.1NTBTindexvalidated
MONDO0002878Evalidated
UMLSC4707554Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card