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Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab
We report a patient with idiopathic hypereosinophilic syndrome (I‐HES) who achieved remission with benralizumab after relapsing on mepolizumab. An 83‐year‐old man was admitted to Showa General Hospital after presenting with hypoxaemia and multiple erythematous lesions. He showed a marked increase in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511777/ https://www.ncbi.nlm.nih.gov/pubmed/33005423 http://dx.doi.org/10.1002/rcr2.665 |
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author | Fujii, Koki Takahashi, Hidenori Hayakawa, Nami Iwasaki, Yoshinobu |
author_facet | Fujii, Koki Takahashi, Hidenori Hayakawa, Nami Iwasaki, Yoshinobu |
author_sort | Fujii, Koki |
collection | PubMed |
description | We report a patient with idiopathic hypereosinophilic syndrome (I‐HES) who achieved remission with benralizumab after relapsing on mepolizumab. An 83‐year‐old man was admitted to Showa General Hospital after presenting with hypoxaemia and multiple erythematous lesions. He showed a marked increase in blood eosinophil count. Skin biopsy revealed an invasion of eosinophils in the dermis. He was diagnosed with I‐HES. He was commenced on prednisolone 40 mg/day with a plan to wean this over time after pulse steroid therapy for three days. Mepolizumab was added when the prednisolone dose was 25 mg/day. Unfortunately, at a prednisolone dose of 5 mg/day, there was evidence of disease progression and the patient was switched to benralizumab. Prednisolone was tapered again and, finally, the patient was in remission. Benralizumab targets interleukin (IL)‐5R and induces antibody‐dependent cell‐mediated cytotoxicity, thereby reducing the eosinophil counts in the tissue. This can be attributed to the therapeutic efficacy against I‐HES. We believe this report may help develop novel therapeutic strategies for I‐HES. |
format | Online Article Text |
id | pubmed-7511777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75117772020-09-30 Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab Fujii, Koki Takahashi, Hidenori Hayakawa, Nami Iwasaki, Yoshinobu Respirol Case Rep Case Reports We report a patient with idiopathic hypereosinophilic syndrome (I‐HES) who achieved remission with benralizumab after relapsing on mepolizumab. An 83‐year‐old man was admitted to Showa General Hospital after presenting with hypoxaemia and multiple erythematous lesions. He showed a marked increase in blood eosinophil count. Skin biopsy revealed an invasion of eosinophils in the dermis. He was diagnosed with I‐HES. He was commenced on prednisolone 40 mg/day with a plan to wean this over time after pulse steroid therapy for three days. Mepolizumab was added when the prednisolone dose was 25 mg/day. Unfortunately, at a prednisolone dose of 5 mg/day, there was evidence of disease progression and the patient was switched to benralizumab. Prednisolone was tapered again and, finally, the patient was in remission. Benralizumab targets interleukin (IL)‐5R and induces antibody‐dependent cell‐mediated cytotoxicity, thereby reducing the eosinophil counts in the tissue. This can be attributed to the therapeutic efficacy against I‐HES. We believe this report may help develop novel therapeutic strategies for I‐HES. John Wiley & Sons, Ltd 2020-09-23 /pmc/articles/PMC7511777/ /pubmed/33005423 http://dx.doi.org/10.1002/rcr2.665 Text en © 2020 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology. This is an open access article under the terms of the http://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 Fujii, Koki Takahashi, Hidenori Hayakawa, Nami Iwasaki, Yoshinobu Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title | Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title_full | Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title_fullStr | Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title_full_unstemmed | Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title_short | Idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
title_sort | idiopathic hypereosinophilic syndrome in remission with benralizumab treatment after relapse with mepolizumab |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511777/ https://www.ncbi.nlm.nih.gov/pubmed/33005423 http://dx.doi.org/10.1002/rcr2.665 |
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