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Autoimmune Progesterone Dermatitis: A Case Report

Background. Autoimmune progesterone dermatitis is a rare cyclic premenstrual allergic reaction to progesterone produced during the luteal phase of a woman's menstrual cycle. Patients present with a variety of conditions including erythema multiforme, eczema, urticaria, angioedema, and progester...

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Autores principales: George, Rachana, Badawy, Shawky Z. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423662/
https://www.ncbi.nlm.nih.gov/pubmed/22924142
http://dx.doi.org/10.1155/2012/757854
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author George, Rachana
Badawy, Shawky Z. A.
author_facet George, Rachana
Badawy, Shawky Z. A.
author_sort George, Rachana
collection PubMed
description Background. Autoimmune progesterone dermatitis is a rare cyclic premenstrual allergic reaction to progesterone produced during the luteal phase of a woman's menstrual cycle. Patients present with a variety of conditions including erythema multiforme, eczema, urticaria, angioedema, and progesterone-induced anaphylaxis. Case. Thirty-eight-year-old woman G2P2002 presents with erythema multiforme and urticarial rash one week prior to her menses starting one year after menarche. She was treated with oral contraceptive pills and the symptoms resolved. Conclusion. This is a typical case of progesterone autoimmunity. The diagnosis is based on cyclic nature of the dermatitis. This differentiates the condition from other allergies or systemic diseases with skin manifestations. Inhibition of ovulation in such cases results in decrease in progesterone secretion and prevention of symptoms.
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spelling pubmed-34236622012-08-24 Autoimmune Progesterone Dermatitis: A Case Report George, Rachana Badawy, Shawky Z. A. Case Rep Obstet Gynecol Case Report Background. Autoimmune progesterone dermatitis is a rare cyclic premenstrual allergic reaction to progesterone produced during the luteal phase of a woman's menstrual cycle. Patients present with a variety of conditions including erythema multiforme, eczema, urticaria, angioedema, and progesterone-induced anaphylaxis. Case. Thirty-eight-year-old woman G2P2002 presents with erythema multiforme and urticarial rash one week prior to her menses starting one year after menarche. She was treated with oral contraceptive pills and the symptoms resolved. Conclusion. This is a typical case of progesterone autoimmunity. The diagnosis is based on cyclic nature of the dermatitis. This differentiates the condition from other allergies or systemic diseases with skin manifestations. Inhibition of ovulation in such cases results in decrease in progesterone secretion and prevention of symptoms. Hindawi Publishing Corporation 2012 2012-08-09 /pmc/articles/PMC3423662/ /pubmed/22924142 http://dx.doi.org/10.1155/2012/757854 Text en Copyright © 2012 R. George and S. Z. A. Badawy. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
George, Rachana
Badawy, Shawky Z. A.
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
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423662/
https://www.ncbi.nlm.nih.gov/pubmed/22924142
http://dx.doi.org/10.1155/2012/757854
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