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A Case Report of Familial Extramammary Paget's Disease in Female Siblings

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dc.contributor.authorThanachat Rutnumnoien_US
dc.contributor.authorCharussri Leeyaphanen_US
dc.contributor.otherSiriraj Hospitalen_US
dc.date.accessioned2022-08-04T11:10:40Z
dc.date.available2022-08-04T11:10:40Z
dc.date.issued2021-01-01en_US
dc.description.abstractExtramammary Paget's disease (EMPD) is a rare intraepithelial neoplasm that occurs in apocrine-bearing areas of skin. Most EMPD patients initially present with chronic pruritic eczematous lesions involving genitalia, perineum and perianal area. Familial form of EMPD is extremely rare. Several genetic mutations have been proposed but specific modes of inheritance are still unknown. This article reports two cases of familial extramammary Paget's disease in female siblings.en_US
dc.identifier.citationCase Reports in Dermatology. Vol.13, No.1 (2021), 176-183en_US
dc.identifier.doi10.1159/000514253en_US
dc.identifier.issn16626567en_US
dc.identifier.other2-s2.0-85103434110en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/78779
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85103434110&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleA Case Report of Familial Extramammary Paget's Disease in Female Siblingsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85103434110&origin=inwarden_US

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