raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213802

Rhabdomyosarcoma of the cervix uteri

Synonyms: Cervical rhabdomyosarcoma

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

Rhabdomyosarcoma of the cervix uteri is a rare, highly malignant soft tissue sarcoma located in the uterine cervix and arising from primitive mesenchymal cells displaying skeletal muscle differentiation. It most often presents with abnormal vaginal discharge or dysfunctional uterine bleeding, abdominal pain and/or a cervical mass protruding into the vagina. Association with DICER1 syndrome has been reported.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRhabdomyosarcoma of the cervix uteriCervical rhabdomyosarcoma
frRhabdomyosarcome du col de l'utérusRhabdomyosarcome cervical
deRhabdomyosarkom der Cervix uteriRhabdomyosarkom, zervikales
esRabdomiosarcoma de cuello de úteroRabdomiosarcoma cervical
itRabdomiosarcoma della cervice uterinaRabdomiosarcoma cervicale
nlRhabdomyosarcoom van cervix uteriCervicaal rhabdomyosarcoom · Rhabdomyosarcoom van baarmoederhals
ptRabdomiossarcoma do colo do útero
plMięsak prążkowanokomórkowy szyjki macicyMięsak prążkowanokomórkowy szyjki
csRhabdomyosarkom hrdla děložníhoCervikální rhabdomyosarkom
ukРабдоміосаркома шийки маткиРабдоміосаркома шийки матки
zh子宫颈横纹肌肉瘤宫颈横纹肌肉瘤
trRahim ağzı uteri rabdomyosarkomuServikal rabdomyosarkom

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C53.0BTNTattributedvalidated
ICD-10C53.1BTNTattributedvalidated
ICD-10C53.8BTNTattributedvalidated
ICD-112B55.YNTBTindexvalidated
MONDO0016282Evalidated
UMLSC4289809Evalidated

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