Extramammary Paget disease

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Extramammary Paget disease

ORPHA:2800Disease

What it is

A rare skin tumor characterized by predominantly intraepithelial growth of an adenocarcinoma which may either arise primarily in the skin (primary extramammary Paget disease) or result from intraepithelial spread of a visceral carcinoma (secondary extramammary Paget disease). The lesion is typically located in the anogenital region, presenting as a scaly, oozing, pruritic or painful erythematous plaque often resembling eczema. It may exhibit an invasive component with a significant risk of lymph node metastasis.

Key facts

Age of onset
Adult, Elderly
Classified as
Disease

Gene

ERBB2Disease-causing somatic mutation(s)

ICD-10 codes

C44.5filed under a broader ICD-10 category

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 4192MEDDRA 10068223MESH D010145MONDO 0008177OMIM 167300UMLS C0030186

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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