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Autoimmune Progesterone Dermatitis: A Case Report

Introduction Autoimmune progesterone dermatitis (APD) is a rare autoimmune dermatosis characterized by recurrent cutaneous and mucosal lesions during the luteal phase of the menstrual cycle that disappear some days after the menses. Case Report A 34-year-old primipara woman with no significant past...

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Autores principales: Özdemir, Özhan, Yahşi, Gözde Girgin, Atalay, Cemal Reşat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Revinter Publicações Ltda 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309278/
https://www.ncbi.nlm.nih.gov/pubmed/30939605
http://dx.doi.org/10.1055/s-0039-1678589
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author Özdemir, Özhan
Yahşi, Gözde Girgin
Atalay, Cemal Reşat
author_facet Özdemir, Özhan
Yahşi, Gözde Girgin
Atalay, Cemal Reşat
author_sort Özdemir, Özhan
collection PubMed
description Introduction Autoimmune progesterone dermatitis (APD) is a rare autoimmune dermatosis characterized by recurrent cutaneous and mucosal lesions during the luteal phase of the menstrual cycle that disappear some days after the menses. Case Report A 34-year-old primipara woman with no significant past medical history and no prior exogenous hormone use, who presented with cyclic skin eruptions starting 1 year after the delivery. The lesions occurred ∼ 6 days before the menses and disappeared in between 1 and 2 days after the menstruation ceased. The patient was diagnosed after a positive response to an intradermal test with progesterone and was successfully treated with combined oral contraceptives. The skin eruptions have not returned since the initiation of this therapy. Conclusion Dermatologists, gynecologists, and obstetricians should be aware of this rare entity. Furthermore, if this condition is suspected, a thorough history taking on the menstrual cycle and results of the intradermal progesterone test are mandatory.
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spelling pubmed-103092782023-07-27 Autoimmune Progesterone Dermatitis: A Case Report Özdemir, Özhan Yahşi, Gözde Girgin Atalay, Cemal Reşat Rev Bras Ginecol Obstet Introduction Autoimmune progesterone dermatitis (APD) is a rare autoimmune dermatosis characterized by recurrent cutaneous and mucosal lesions during the luteal phase of the menstrual cycle that disappear some days after the menses. Case Report A 34-year-old primipara woman with no significant past medical history and no prior exogenous hormone use, who presented with cyclic skin eruptions starting 1 year after the delivery. The lesions occurred ∼ 6 days before the menses and disappeared in between 1 and 2 days after the menstruation ceased. The patient was diagnosed after a positive response to an intradermal test with progesterone and was successfully treated with combined oral contraceptives. The skin eruptions have not returned since the initiation of this therapy. Conclusion Dermatologists, gynecologists, and obstetricians should be aware of this rare entity. Furthermore, if this condition is suspected, a thorough history taking on the menstrual cycle and results of the intradermal progesterone test are mandatory. Thieme Revinter Publicações Ltda 2019-04-02 2019-03 /pmc/articles/PMC10309278/ /pubmed/30939605 http://dx.doi.org/10.1055/s-0039-1678589 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Özdemir, Özhan
Yahşi, Gözde Girgin
Atalay, Cemal Reşat
Autoimmune Progesterone Dermatitis: A Case Report
title Autoimmune Progesterone Dermatitis: A Case Report
title_full Autoimmune Progesterone Dermatitis: A Case Report
title_fullStr Autoimmune Progesterone Dermatitis: A Case Report
title_full_unstemmed Autoimmune Progesterone Dermatitis: A Case Report
title_short Autoimmune Progesterone Dermatitis: A Case Report
title_sort autoimmune progesterone dermatitis: a case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309278/
https://www.ncbi.nlm.nih.gov/pubmed/30939605
http://dx.doi.org/10.1055/s-0039-1678589
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