raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213792

Adenosarcoma of the cervix uteri

Synonyms: Cervical adenosarcoma

Type
Disease
Group
Disorder
Age of onset
Adolescent, Adult, Elderly
Status
active

A rare subtype of malignant mixed epithelial and mesenchymal tumor composed of benign or mildly atypical glandular elements and a surrounding low-grade malignant stroma, often containing heterologous elements, such as areas of sex-cord-like or smooth muscle differentiation. It usually presents with vaginal bleeding or discharge, lower abdominal pain and/or a cervical mass or polyp. The tumor may arise from pre-existing endometriosis and patients may have a history of recurrent cervical polyps.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAdenosarcoma of the cervix uteriCervical adenosarcoma
frAdénosarcome du col de l'utérusAdénosarcome cervical
deAdenosarkom der Cervix uteriAdenosarkom, zervikales
esAdenosarcoma de cuello de úteroAdenosarcoma cervical
itAdenosarcoma della cervice uterinaAdenosarcoma cervicale
nlAdenosarcoom van cervix uteriAdenosarcoom van baarmoederhals · Cervicaal adenosarcoom
ptAdenossarcoma do colo do útero
plGruczolakomięsak szyjki macicyGruczolakomięsak szyjki
csAdenosarkom hrdla děložníhoCervikální adenosarkom
ukАденосаркома шийки маткиАденосаркома шийки матки
zh子宫颈腺肉瘤宫颈腺肉瘤
trServiks uteri adenosarkomuServikal adenosarkom

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C53.0BTNTattributedvalidated
ICD-10C53.1BTNTattributedvalidated
ICD-10C53.8BTNTattributedvalidated
ICD-112C77.YNTBTindexvalidated
MONDO0002876Evalidated
UMLSC1516426Evalidated

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

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 000—WorldwideClass onlyValidatedORPHANET_19685064[PMID]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card