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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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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. |
format | Online Article Text |
id | pubmed-3423662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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