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Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report

INTRODUCTION: Immediate-type hypersensitivity to glucocorticosteroids is rare but well known among allergists. Surprisingly, very few reports of glucocorticosteroid hypersensitivity in children exist although glucocorticosteroid treatment is particularly common in this age group. CASE PRESENTATION:...

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Autores principales: Lehmann, Sylvia, Ott, Hagen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441637/
https://www.ncbi.nlm.nih.gov/pubmed/18518974
http://dx.doi.org/10.1186/1752-1947-2-186
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author Lehmann, Sylvia
Ott, Hagen
author_facet Lehmann, Sylvia
Ott, Hagen
author_sort Lehmann, Sylvia
collection PubMed
description INTRODUCTION: Immediate-type hypersensitivity to glucocorticosteroids is rare but well known among allergists. Surprisingly, very few reports of glucocorticosteroid hypersensitivity in children exist although glucocorticosteroid treatment is particularly common in this age group. CASE PRESENTATION: We report the case of a 2-year-old boy who developed generalized urticaria, facial angio-oedema, nausea and severe dyspnoea after intravenous application of prednisolone-21-hydrogen succinate. Skin prick testing with prednisolone-21-hydrogen succinate elicited a positive result; no reactions were observed to prednisone, betamethasone or dexamethasone. While fluorescence enzyme immunoassay analysis revealed no specific IgE antibodies against prednisolone-21-hydrogen succinate, CD63-based basophil activation testing with the culprit drug prednisolone-21-hydrogen succinate was positive. In contrast, additional incubation of basophils with prednisone, betamethasone and dexamethasone did not elicit any significant response. Hence, we performed an oral provocation test with betamethasone and a titrated intravenous dexamethasone challenge. As both drugs were tolerated without any complications they were recommended for future treatment. CONCLUSION: In a child with confirmed immediate-type hypersensitivity to glucocorticosteroids, it is still not possible to predict which glucocorticosteroid might be tolerated by solely relying on clinical history or results of skin and in vitro testing. Therefore, incremental glucocorticosteroid challenges under standardized clinical conditions remain necessary in order to facilitate a patient-tailored emergency treatment and to avoid severe reactions to glucocorticosteroids in these patients.
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spelling pubmed-24416372008-06-28 Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report Lehmann, Sylvia Ott, Hagen J Med Case Reports Case Report INTRODUCTION: Immediate-type hypersensitivity to glucocorticosteroids is rare but well known among allergists. Surprisingly, very few reports of glucocorticosteroid hypersensitivity in children exist although glucocorticosteroid treatment is particularly common in this age group. CASE PRESENTATION: We report the case of a 2-year-old boy who developed generalized urticaria, facial angio-oedema, nausea and severe dyspnoea after intravenous application of prednisolone-21-hydrogen succinate. Skin prick testing with prednisolone-21-hydrogen succinate elicited a positive result; no reactions were observed to prednisone, betamethasone or dexamethasone. While fluorescence enzyme immunoassay analysis revealed no specific IgE antibodies against prednisolone-21-hydrogen succinate, CD63-based basophil activation testing with the culprit drug prednisolone-21-hydrogen succinate was positive. In contrast, additional incubation of basophils with prednisone, betamethasone and dexamethasone did not elicit any significant response. Hence, we performed an oral provocation test with betamethasone and a titrated intravenous dexamethasone challenge. As both drugs were tolerated without any complications they were recommended for future treatment. CONCLUSION: In a child with confirmed immediate-type hypersensitivity to glucocorticosteroids, it is still not possible to predict which glucocorticosteroid might be tolerated by solely relying on clinical history or results of skin and in vitro testing. Therefore, incremental glucocorticosteroid challenges under standardized clinical conditions remain necessary in order to facilitate a patient-tailored emergency treatment and to avoid severe reactions to glucocorticosteroids in these patients. BioMed Central 2008-06-02 /pmc/articles/PMC2441637/ /pubmed/18518974 http://dx.doi.org/10.1186/1752-1947-2-186 Text en Copyright © 2008 Lehmann and Ott; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lehmann, Sylvia
Ott, Hagen
Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title_full Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title_fullStr Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title_full_unstemmed Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title_short Glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
title_sort glucocorticoid hypersensitivity as a rare but potentially fatal side effect of paediatric asthma treatment: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441637/
https://www.ncbi.nlm.nih.gov/pubmed/18518974
http://dx.doi.org/10.1186/1752-1947-2-186
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