raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:498228

Phyllodes tumor of the prostate

Synonyms: Cystic epithelial-stromal tumors of the prostate · Cystosarcoma phyllodes of the prostate · Phyllodes type of atypical prostatic hyperplasia

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

A rare urogenital tumor characterized by stromal and epithelial components forming cysts lined by hyperplastic epithelium in a cellular or sarcomatoid stroma. The tumors may be clinically benign or malignant and tend to recur after transurethral resection. Metastatic spread is to lungs, bone, and liver. Patients may present with obstructive voiding symptoms, dysuria, hematuria, urinary retention, or a palpable abdominal mass. The prostate is palpably enlarged but feels soft and spongy.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPhyllodes tumor of the prostateCystic epithelial-stromal tumors of the prostate · Cystosarcoma phyllodes of the prostate · Phyllodes type of atypical prostatic hyperplasia
frTumeur phyllode de la prostateCystosarcome phyllode de la prostate · Cystosarcome phylloïde de la prostate · Tumeur phylloïde de la prostate
dePhylloidtumor der ProstataCystosarcoma phyllodes der Prostata
esTumor filoides de la próstataCistosarcoma filoides de la próstata
itTumore filloide della prostata
nlPhyllodestumor van prostaatAtypische hyperplasie van prostaat, phyllodes-type · Cystische epitheliale-stromale tumoren van prostaat · Cystosarcoma phyllodes van prostaat
ptTumor filóide da próstata
plGuz liściasty prostaty= en
csPhyllodes tumor prostaty= en
ukФіброзна пухлина передміхурової залозиКістозні епітеліально-стромальні пухлини передміхурової залози · Фіброаденома передміхурової залози · Аденома передміхурової залози за типом Філлодеса
zh前列腺叶状肿瘤叶状不典型前列腺增生
trProstatın filloid tümörüProstatın sistosarkom filodları · Prostatın kistik epitel-stromal tümörleri · Atipik prostat hiperplazisinin filloid tipi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C61NTBTattributedvalidated
ICD-112C82.YNTBTattributedvalidated
MONDO0021102Evalidated
UMLSC1335409Evalidated
GARD9404Evalidated

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
Cases/families90 casesWorldwideCase(s)Validated25210561[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