A Case Report of Familial Extramammary Paget's Disease in Female Siblings
Extramammary 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 geneti...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Karger Publishers
2021-03-01
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| Series: | Case Reports in Dermatology |
| Subjects: | |
| Online Access: | https://www.karger.com/Article/FullText/514253 |
| _version_ | 1818958775745249280 |
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| author | Thanachat Rutnumnoi Charussri Leeyaphan |
| author_facet | Thanachat Rutnumnoi Charussri Leeyaphan |
| author_sort | Thanachat Rutnumnoi |
| collection | DOAJ |
| description | Extramammary 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. |
| first_indexed | 2024-12-20T11:31:07Z |
| format | Article |
| id | doaj.art-220b520813b04b3c8c25a77ec2bf5390 |
| institution | Directory Open Access Journal |
| issn | 1662-6567 |
| language | English |
| last_indexed | 2024-12-20T11:31:07Z |
| publishDate | 2021-03-01 |
| publisher | Karger Publishers |
| record_format | Article |
| series | Case Reports in Dermatology |
| spelling | doaj.art-220b520813b04b3c8c25a77ec2bf53902022-12-21T19:42:14ZengKarger PublishersCase Reports in Dermatology1662-65672021-03-0113117618310.1159/000514253514253A Case Report of Familial Extramammary Paget's Disease in Female SiblingsThanachat RutnumnoiCharussri LeeyaphanExtramammary 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.https://www.karger.com/Article/FullText/514253familial extramammary paget’s diseaseextramammary paget’s diseasepaget’s disease of the vulvar |
| spellingShingle | Thanachat Rutnumnoi Charussri Leeyaphan A Case Report of Familial Extramammary Paget's Disease in Female Siblings Case Reports in Dermatology familial extramammary paget’s disease extramammary paget’s disease paget’s disease of the vulvar |
| title | A Case Report of Familial Extramammary Paget's Disease in Female Siblings |
| title_full | A Case Report of Familial Extramammary Paget's Disease in Female Siblings |
| title_fullStr | A Case Report of Familial Extramammary Paget's Disease in Female Siblings |
| title_full_unstemmed | A Case Report of Familial Extramammary Paget's Disease in Female Siblings |
| title_short | A Case Report of Familial Extramammary Paget's Disease in Female Siblings |
| title_sort | case report of familial extramammary paget s disease in female siblings |
| topic | familial extramammary paget’s disease extramammary paget’s disease paget’s disease of the vulvar |
| url | https://www.karger.com/Article/FullText/514253 |
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