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Pemphigoid gestationis and intravenous immunoglobulin therapy()
Pemphigoid gestationis, which is also known as herpes gestationis, is a rare, pregnancy-associated, autoimmune bullous disease. Treatment depends on the severity of the disease for each patient and the safety and use of these drugs during pregnancy and breastfeeding must be taken into consideration...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116823/ https://www.ncbi.nlm.nih.gov/pubmed/30175219 http://dx.doi.org/10.1016/j.ijwd.2018.03.007 |
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author | Yang, Anes Uhlenhake, Elizabeth Murrell, Dedee F. |
author_facet | Yang, Anes Uhlenhake, Elizabeth Murrell, Dedee F. |
author_sort | Yang, Anes |
collection | PubMed |
description | Pemphigoid gestationis, which is also known as herpes gestationis, is a rare, pregnancy-associated, autoimmune bullous disease. Treatment depends on the severity of the disease for each patient and the safety and use of these drugs during pregnancy and breastfeeding must be taken into consideration to guide their use. We describe the therapeutic response of two cases of pemphigoid gestationis that did not respond to conventional immunosuppressive therapy or adverse effects limited their use. Both patients eventually received treatment with intravenous immunoglobulin therapy, which resulted in clinical remission. This clinical improvement with disappearance of lesions and a reduction in pruritus was paralleled in a decline in Bullous Pemphigoid Disease Activity Index activity scores, which is a validated scoring system to measure the related condition, bullous pemphigoid. |
format | Online Article Text |
id | pubmed-6116823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61168232018-08-31 Pemphigoid gestationis and intravenous immunoglobulin therapy() Yang, Anes Uhlenhake, Elizabeth Murrell, Dedee F. Int J Womens Dermatol Article Pemphigoid gestationis, which is also known as herpes gestationis, is a rare, pregnancy-associated, autoimmune bullous disease. Treatment depends on the severity of the disease for each patient and the safety and use of these drugs during pregnancy and breastfeeding must be taken into consideration to guide their use. We describe the therapeutic response of two cases of pemphigoid gestationis that did not respond to conventional immunosuppressive therapy or adverse effects limited their use. Both patients eventually received treatment with intravenous immunoglobulin therapy, which resulted in clinical remission. This clinical improvement with disappearance of lesions and a reduction in pruritus was paralleled in a decline in Bullous Pemphigoid Disease Activity Index activity scores, which is a validated scoring system to measure the related condition, bullous pemphigoid. Elsevier 2018-05-03 /pmc/articles/PMC6116823/ /pubmed/30175219 http://dx.doi.org/10.1016/j.ijwd.2018.03.007 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Yang, Anes Uhlenhake, Elizabeth Murrell, Dedee F. Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title | Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title_full | Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title_fullStr | Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title_full_unstemmed | Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title_short | Pemphigoid gestationis and intravenous immunoglobulin therapy() |
title_sort | pemphigoid gestationis and intravenous immunoglobulin therapy() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116823/ https://www.ncbi.nlm.nih.gov/pubmed/30175219 http://dx.doi.org/10.1016/j.ijwd.2018.03.007 |
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