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A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
In the therapeutic management of eosinophilic disorder, it is important to prevent hypereosinophilia (HE)‐related organ damage even in the process of diagnosis. We describe here a unique clinical and histopathological findings of the patient with HE accompanied with digital ischaemia. Treatment with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060027/ https://www.ncbi.nlm.nih.gov/pubmed/35664976 http://dx.doi.org/10.1002/ski2.32 |
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author | Kaga, M. Takeuchi, H. Iwahara, K. Ihara, H. |
author_facet | Kaga, M. Takeuchi, H. Iwahara, K. Ihara, H. |
author_sort | Kaga, M. |
collection | PubMed |
description | In the therapeutic management of eosinophilic disorder, it is important to prevent hypereosinophilia (HE)‐related organ damage even in the process of diagnosis. We describe here a unique clinical and histopathological findings of the patient with HE accompanied with digital ischaemia. Treatment with intravenous prostaglandin E(1) was essential for digital ischaemia in our case while benralizumab, humanized monoclonal antibody against interleukin‐5 receptorα, did not affect. Our case suggests an earlier intervention for digital ischaemia in the therapeutic management of eosiniphilic disorder. |
format | Online Article Text |
id | pubmed-9060027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90600272022-06-04 A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1) Kaga, M. Takeuchi, H. Iwahara, K. Ihara, H. Skin Health Dis Case Reports In the therapeutic management of eosinophilic disorder, it is important to prevent hypereosinophilia (HE)‐related organ damage even in the process of diagnosis. We describe here a unique clinical and histopathological findings of the patient with HE accompanied with digital ischaemia. Treatment with intravenous prostaglandin E(1) was essential for digital ischaemia in our case while benralizumab, humanized monoclonal antibody against interleukin‐5 receptorα, did not affect. Our case suggests an earlier intervention for digital ischaemia in the therapeutic management of eosiniphilic disorder. John Wiley and Sons Inc. 2021-05-03 /pmc/articles/PMC9060027/ /pubmed/35664976 http://dx.doi.org/10.1002/ski2.32 Text en © 2021 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Kaga, M. Takeuchi, H. Iwahara, K. Ihara, H. A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1) |
title | A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
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title_full | A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
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title_fullStr | A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
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title_full_unstemmed | A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
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title_short | A case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin E(1)
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title_sort | case of hypereosinophilia with digital ischaemia successfully treated with intravenous prostaglandin e(1) |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060027/ https://www.ncbi.nlm.nih.gov/pubmed/35664976 http://dx.doi.org/10.1002/ski2.32 |
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