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Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report
Linear IgA/IgG bullous dermatosis (LAGBD) is a rare, autoimmune blistering skin disease. We report a case of LAGBD in a 70‐year‐old woman. All common treatments were discontinued due to side effects or lack of treatment response. The patient was successfully treated with omalizumab which cleared her...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905130/ https://www.ncbi.nlm.nih.gov/pubmed/35280104 http://dx.doi.org/10.1002/ccr3.5368 |
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author | Haulrig, Morten Bahrt Nielsen, Signe Ledou Elberling, Jesper Skov, Lone |
author_facet | Haulrig, Morten Bahrt Nielsen, Signe Ledou Elberling, Jesper Skov, Lone |
author_sort | Haulrig, Morten Bahrt |
collection | PubMed |
description | Linear IgA/IgG bullous dermatosis (LAGBD) is a rare, autoimmune blistering skin disease. We report a case of LAGBD in a 70‐year‐old woman. All common treatments were discontinued due to side effects or lack of treatment response. The patient was successfully treated with omalizumab which cleared her lesions after three months. |
format | Online Article Text |
id | pubmed-8905130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89051302022-03-10 Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report Haulrig, Morten Bahrt Nielsen, Signe Ledou Elberling, Jesper Skov, Lone Clin Case Rep Case Reports Linear IgA/IgG bullous dermatosis (LAGBD) is a rare, autoimmune blistering skin disease. We report a case of LAGBD in a 70‐year‐old woman. All common treatments were discontinued due to side effects or lack of treatment response. The patient was successfully treated with omalizumab which cleared her lesions after three months. John Wiley and Sons Inc. 2022-03-08 /pmc/articles/PMC8905130/ /pubmed/35280104 http://dx.doi.org/10.1002/ccr3.5368 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Haulrig, Morten Bahrt Nielsen, Signe Ledou Elberling, Jesper Skov, Lone Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title | Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title_full | Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title_fullStr | Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title_full_unstemmed | Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title_short | Linear IgA/IgG bullous dermatosis successfully treated with omalizumab: A case report |
title_sort | linear iga/igg bullous dermatosis successfully treated with omalizumab: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905130/ https://www.ncbi.nlm.nih.gov/pubmed/35280104 http://dx.doi.org/10.1002/ccr3.5368 |
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