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Cough in hypereosinophilic syndrome: case report and literature review
BACKGROUND: Cough and airway eosinophilic inflammation has not been highlighted in hypereosinophilic syndrome (HES). CASE PRESENTATION: We report 2 further cases and reviewed the clinical features and treatment of HES present with cough from the literature. Both cases were middle age male, presentin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158094/ https://www.ncbi.nlm.nih.gov/pubmed/32293378 http://dx.doi.org/10.1186/s12890-020-1134-x |
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author | Xie, Jiaxing Zhang, Jianheng Zhang, Xiaoxian Zhang, Qingling Chung, Kian Fan Wang, Chunyan Lai, Kefang |
author_facet | Xie, Jiaxing Zhang, Jianheng Zhang, Xiaoxian Zhang, Qingling Chung, Kian Fan Wang, Chunyan Lai, Kefang |
author_sort | Xie, Jiaxing |
collection | PubMed |
description | BACKGROUND: Cough and airway eosinophilic inflammation has not been highlighted in hypereosinophilic syndrome (HES). CASE PRESENTATION: We report 2 further cases and reviewed the clinical features and treatment of HES present with cough from the literature. Both cases were middle age male, presenting with chronic cough, airway eosinophilic inflammation and hyper eosinophilia who have been previous misdiagnosed as cough-variant asthma and failed anti-asthma treatment. PDGFRA fusion gene was confirmed in one case, but not in the other case. Both had evidence of myeloproliferative features. The tyrosine kinase inhibitor, imatinib, resulted in complete resolution of eosinophilia and cough. By searching PubMed, we found 8 HES cohorts of 411 cases between 1975 and 2013, where the incidence of cough was 23.11%. Sixteen case reports of HES presented with cough as predominant or sole symptom, with nine male patients with positive PDGFRA fusion gene, who responded well to imatinib. Six of seven patients, who tested negative for the PDGFRA, responded to systemic glucocorticoids. CONCLUSIONS: Cough and airway eosinophilic inflammation is common in some HES patients. PDGFRA+ HES patients present with chronic cough respond well to imatinib. Our case reports indicate that PDGFRA negative HES patients may respond to imatinib as well. |
format | Online Article Text |
id | pubmed-7158094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71580942020-04-21 Cough in hypereosinophilic syndrome: case report and literature review Xie, Jiaxing Zhang, Jianheng Zhang, Xiaoxian Zhang, Qingling Chung, Kian Fan Wang, Chunyan Lai, Kefang BMC Pulm Med Case Report BACKGROUND: Cough and airway eosinophilic inflammation has not been highlighted in hypereosinophilic syndrome (HES). CASE PRESENTATION: We report 2 further cases and reviewed the clinical features and treatment of HES present with cough from the literature. Both cases were middle age male, presenting with chronic cough, airway eosinophilic inflammation and hyper eosinophilia who have been previous misdiagnosed as cough-variant asthma and failed anti-asthma treatment. PDGFRA fusion gene was confirmed in one case, but not in the other case. Both had evidence of myeloproliferative features. The tyrosine kinase inhibitor, imatinib, resulted in complete resolution of eosinophilia and cough. By searching PubMed, we found 8 HES cohorts of 411 cases between 1975 and 2013, where the incidence of cough was 23.11%. Sixteen case reports of HES presented with cough as predominant or sole symptom, with nine male patients with positive PDGFRA fusion gene, who responded well to imatinib. Six of seven patients, who tested negative for the PDGFRA, responded to systemic glucocorticoids. CONCLUSIONS: Cough and airway eosinophilic inflammation is common in some HES patients. PDGFRA+ HES patients present with chronic cough respond well to imatinib. Our case reports indicate that PDGFRA negative HES patients may respond to imatinib as well. BioMed Central 2020-04-15 /pmc/articles/PMC7158094/ /pubmed/32293378 http://dx.doi.org/10.1186/s12890-020-1134-x Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Xie, Jiaxing Zhang, Jianheng Zhang, Xiaoxian Zhang, Qingling Chung, Kian Fan Wang, Chunyan Lai, Kefang Cough in hypereosinophilic syndrome: case report and literature review |
title | Cough in hypereosinophilic syndrome: case report and literature review |
title_full | Cough in hypereosinophilic syndrome: case report and literature review |
title_fullStr | Cough in hypereosinophilic syndrome: case report and literature review |
title_full_unstemmed | Cough in hypereosinophilic syndrome: case report and literature review |
title_short | Cough in hypereosinophilic syndrome: case report and literature review |
title_sort | cough in hypereosinophilic syndrome: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158094/ https://www.ncbi.nlm.nih.gov/pubmed/32293378 http://dx.doi.org/10.1186/s12890-020-1134-x |
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