raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213807

Leiomyosarcoma of the cervix uteri

Synonyms: Cervical leiomyosarcoma

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

Leiomyosarcoma of the cervix uteri is a rare, malignant mesenchymal tumor of smooth muscle origin, macroscopically appearing as a large, poorly circumscribed mass, often protruding from the cervical canal or expanding it circumferentially. The most common presenting symptoms are vaginal discharge or bleeding, pain in the lower abdomen and a bulky cervical mass. There is a reported tendency to metastatsize hematogenously, especially to the lungs, peritoneum, bones and the liver.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enLeiomyosarcoma of the cervix uteriCervical leiomyosarcoma
frLéiomyosarcome du col de l'utérusLéiomyosarcome cervical
deLeiomyosarkom der Cervix uteriLeiomyosarkom, zervikales
esLeiomiosarcoma de cuello de úteroLeiomiosarcoma cervical
itLeiomiosarcoma della cervice uterinaLeiomiosarcoma cervicale
nlLeiomyosarcoom van cervix uteriCervicaal leiomyosarcoom · Leiomyosarcoom van baarmoederhals
ptLeiomiossarcoma do colo do útero
plMięsak głoadkokomórkowy szyjki macicyMięsak głoadkokomórkowy szyjki
csLeiomyosarkom hrdla děložníhoCervikální leiomyosarkom
ukЛейоміосаркома шийки маткиЛейоміосаркома шийки матки
zh子宫颈平滑肌肉瘤宫颈平滑肌肉瘤
trServiks uteri leiomyosarkomuServikal leiomyosarkom

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C53.0BTNTattributedvalidated
ICD-10C53.1BTNTattributedvalidated
ICD-10C53.8BTNTattributedvalidated
ICD-112B58.1NTBTindexvalidated
MONDO0016283Evalidated
UMLSC4289817Evalidated

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_23519508[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