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Suspicion of pulmonary embolism during treatment of pemphigoid gestationis

Pemphigoid gestationis (PG), first described in 1872 by Laws Milton, is a rare autoimmune bullous disease of pregnancy and puerperium. Pemphigoid gestationis has been estimated to occur in 1: 50 000 pregnancies and usually presents in the second or third trimester with exacerbation after partum. Thi...

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Autores principales: Podolec-Rubiś, Magdalena, Wołek, Marta, Brzewski, Paweł, Wojas-Pelc, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834694/
https://www.ncbi.nlm.nih.gov/pubmed/24278048
http://dx.doi.org/10.5114/pdia.2013.33381
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author Podolec-Rubiś, Magdalena
Wołek, Marta
Brzewski, Paweł
Wojas-Pelc, Anna
author_facet Podolec-Rubiś, Magdalena
Wołek, Marta
Brzewski, Paweł
Wojas-Pelc, Anna
author_sort Podolec-Rubiś, Magdalena
collection PubMed
description Pemphigoid gestationis (PG), first described in 1872 by Laws Milton, is a rare autoimmune bullous disease of pregnancy and puerperium. Pemphigoid gestationis has been estimated to occur in 1: 50 000 pregnancies and usually presents in the second or third trimester with exacerbation after partum. This disease is caused by circulating IgG1 immunoglobulin against hemidesmosomal protein bullous pemphigoid BP180 (BPAG2) type XVII collagen and less frequently BP230. We present a case of pemphigoid gestationis in primigravida with complications during treatment due to the suspicion of pulmonary embolism.
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spelling pubmed-38346942013-11-25 Suspicion of pulmonary embolism during treatment of pemphigoid gestationis Podolec-Rubiś, Magdalena Wołek, Marta Brzewski, Paweł Wojas-Pelc, Anna Postepy Dermatol Alergol Case Report Pemphigoid gestationis (PG), first described in 1872 by Laws Milton, is a rare autoimmune bullous disease of pregnancy and puerperium. Pemphigoid gestationis has been estimated to occur in 1: 50 000 pregnancies and usually presents in the second or third trimester with exacerbation after partum. This disease is caused by circulating IgG1 immunoglobulin against hemidesmosomal protein bullous pemphigoid BP180 (BPAG2) type XVII collagen and less frequently BP230. We present a case of pemphigoid gestationis in primigravida with complications during treatment due to the suspicion of pulmonary embolism. Termedia Publishing House 2013-02-20 2013-02 /pmc/articles/PMC3834694/ /pubmed/24278048 http://dx.doi.org/10.5114/pdia.2013.33381 Text en Copyright © 2013 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Podolec-Rubiś, Magdalena
Wołek, Marta
Brzewski, Paweł
Wojas-Pelc, Anna
Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title_full Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title_fullStr Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title_full_unstemmed Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title_short Suspicion of pulmonary embolism during treatment of pemphigoid gestationis
title_sort suspicion of pulmonary embolism during treatment of pemphigoid gestationis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834694/
https://www.ncbi.nlm.nih.gov/pubmed/24278048
http://dx.doi.org/10.5114/pdia.2013.33381
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