raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213751

Malignant germ cell tumor of the corpus uteri

Synonyms: Germ cell cancer of the corpus uteri

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

Malignant germ cell tumor of the corpus uteri is an extremely rare uterine neoplasm characterized by a typically polypoid mass deriving from primordial germ cells localized in the endometrium. Presentation is non-specific and often includes abnormal vaginal bleeding and/or discharge, a mass protruding from the vagina, abdominal and/or pelvic pain or, less commonly, difficulty passing stool and perianal pain. The malignant teratoma and yolk sac tumor histological subtypes are the most common.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMalignant germ cell tumor of the corpus uteriGerm cell cancer of the corpus uteri
frTumeur germinale maligne du corps de l'utérusCancer germinal du corps de l'utérus
deMaligner Keimzelltumor des Corpus uteriKeimzellkrebs des Corpus uteri
esTumor maligno de células germinales de cuerpo de úteroCáncer de células germinales de cuerpo de útero
itTumore maligno a cellule germinali del corpo dell'uteroCancro a cellule germinali del corpo uterino
nlMaligne kiemceltumor van corpus uteriKiemcelkanker van corpus uteri · Kwaadaardige kiemceltumor van baarmoederlichaam
ptTumor maligno de células germinativas do corpo uterino
plZłośliwy rak zarodkowy trzonu macicyRak zarodkowy trzonu macicy
csZhoubný nádor těla děložního ze zárodečných buněkGerminom hrdla děložního
ukЗлоякісна герміногенна пухлина тіла маткиГерміногенний рак тіла матки
zh子宫体恶性生殖细胞肿瘤子宫体生殖细胞癌
trKorpus uteri'nin habis germ hücre tümörüKorpus uteri'nin germ hücre kanseri

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C54.0BTNTattributedvalidated
ICD-10C54.1BTNTattributedvalidated
ICD-10C54.2BTNTattributedvalidated
ICD-10C54.3BTNTattributedvalidated
ICD-10C54.8BTNTattributedvalidated
ICD-112C76.YNTBTindexvalidated
MONDO0016273Evalidated
UMLSC4750753Evalidated

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