raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:424073

Serous cystadenocarcinoma of pancreas

Synonyms: Pancreatic serous cystadenocarcinoma

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adult
Status
active

A very rare, malignant, epithelial tumor of the pancreas composed of cystic structures lined by glycogen-rich clear cells, associated with local invasiveness often involving the spleen, duodenum and/or stomach and metastatic spread to the liver, peritoneum and/or lymph nodes. Presenting symptoms are variable and usually non-specific and include abdominal and/or flank pain, palpable abdominal mass, upper gastrointestinal bleeding, jaundice or abnormal serum liver enzymes, vomiting, anorexia and/or weight loss.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enSerous cystadenocarcinoma of pancreasPancreatic serous cystadenocarcinoma
frCystadénocarcinome séreux du pancréasCystadénocarcinome séreux pancréatique
deSeröses Zystadenokarzinom des PankreasPankreatisches seröses Zystadenokarzinom · SCN · Serös-zystische Neoplasien des Pankreas
esCistoadenocarcinoma seroso de páncreasCistoadenocarcinoma pancreático seroso
itCistoadenocarcinoma sieroso del pancreasCistoadenocarcinoma pancreatico sieroso
nlSereus cystadenocarcinoom van prancreasPancreatisch sereus cystadenocarcinoom
ptCistoadenocarcinoma seroso do pâncreas
plGruczolakotorbielakorak surowiczy trzustki= en
csSerózní cystadenokarcinom pankreatuPankreatický serózní cystadenokarcinom
ukСерозна цистаденокарцинома підшлункової залозиСерозна цистаденокарцинома підшлункової залози
zh胰腺浆液性囊腺癌胰腺浆液性囊腺癌
trPankreasın seröz kistadenokarsinomuPankreasın seröz kistadenokarsinomu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C25.0BTNTattributedvalidated
ICD-10C25.1BTNTattributedvalidated
ICD-10C25.2BTNTattributedvalidated
ICD-10C25.7BTNTattributedvalidated
ICD-10C25.8BTNTattributedvalidated
ICD-112C10.0NTBTindexvalidated
MONDO0003630Evalidated
UMLSC1335315Evalidated

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

4 records
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 0000.002 / 100 000BelgiumValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]
Annual incidence<1 / 1 000 0000.002 / 100 000FinlandValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]
Annual incidence<1 / 1 000 000—EuropeClass onlyValidatedRARECARE surveillance of rare cancers in Europe[OTHER]
Annual incidence<1 / 1 000 0000.001 / 100 000GermanyValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]

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