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Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature
Autoimmune progesterone dermatitis (APD) is a condition in which the menstrual cycle is associated with a number of skin findings such as urticaria, eczema, angioedema, and others. In affected women, it occurs 3–10 days prior to the onset of menstrual flow, and resolves 2 days into menses. Women wit...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509283/ https://www.ncbi.nlm.nih.gov/pubmed/15287986 http://dx.doi.org/10.1186/1476-7961-2-10 |
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author | Baptist, Alan P Baldwin, James L |
author_facet | Baptist, Alan P Baldwin, James L |
author_sort | Baptist, Alan P |
collection | PubMed |
description | Autoimmune progesterone dermatitis (APD) is a condition in which the menstrual cycle is associated with a number of skin findings such as urticaria, eczema, angioedema, and others. In affected women, it occurs 3–10 days prior to the onset of menstrual flow, and resolves 2 days into menses. Women with irregular menses may not have this clear correlation, and therefore may be missed. We present a case of APD in a woman with irregular menses and urticaria/angioedema for over 20 years, who had not been diagnosed or correctly treated due to the variable timing of skin manifestations and menses. In addition, we review the medical literature in regards to clinical features, pathogenesis, diagnosis, and treatment options. |
format | Text |
id | pubmed-509283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5092832004-08-13 Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature Baptist, Alan P Baldwin, James L Clin Mol Allergy Case Report Autoimmune progesterone dermatitis (APD) is a condition in which the menstrual cycle is associated with a number of skin findings such as urticaria, eczema, angioedema, and others. In affected women, it occurs 3–10 days prior to the onset of menstrual flow, and resolves 2 days into menses. Women with irregular menses may not have this clear correlation, and therefore may be missed. We present a case of APD in a woman with irregular menses and urticaria/angioedema for over 20 years, who had not been diagnosed or correctly treated due to the variable timing of skin manifestations and menses. In addition, we review the medical literature in regards to clinical features, pathogenesis, diagnosis, and treatment options. BioMed Central 2004-08-02 /pmc/articles/PMC509283/ /pubmed/15287986 http://dx.doi.org/10.1186/1476-7961-2-10 Text en Copyright © 2004 Baptist and Baldwin; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Baptist, Alan P Baldwin, James L Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title | Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title_full | Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title_fullStr | Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title_full_unstemmed | Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title_short | Autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
title_sort | autoimmune progesterone dermatitis in a patient with endometriosis: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509283/ https://www.ncbi.nlm.nih.gov/pubmed/15287986 http://dx.doi.org/10.1186/1476-7961-2-10 |
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