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Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome

Kawasaki disease (KD) is rare in infants less than 3 months of age, and its recurrence is exceptional. Infants with KD are at higher risk of severe clinical presentation, therapy failure, complications and coronary aneurysms (CAAs), and this is the reason they deserve more aggressive therapy and a s...

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Autores principales: Bossi, Grazia, Codazzi, Alessia Claudia, Vinci, Federica, Clerici, Edoardo, Regalbuto, Corrado, Crapanzano, Carmela, Veraldi, Daniele, Moiraghi, Alice, Marseglia, Gian Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139195/
https://www.ncbi.nlm.nih.gov/pubmed/35626849
http://dx.doi.org/10.3390/children9050672
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author Bossi, Grazia
Codazzi, Alessia Claudia
Vinci, Federica
Clerici, Edoardo
Regalbuto, Corrado
Crapanzano, Carmela
Veraldi, Daniele
Moiraghi, Alice
Marseglia, Gian Luigi
author_facet Bossi, Grazia
Codazzi, Alessia Claudia
Vinci, Federica
Clerici, Edoardo
Regalbuto, Corrado
Crapanzano, Carmela
Veraldi, Daniele
Moiraghi, Alice
Marseglia, Gian Luigi
author_sort Bossi, Grazia
collection PubMed
description Kawasaki disease (KD) is rare in infants less than 3 months of age, and its recurrence is exceptional. Infants with KD are at higher risk of severe clinical presentation, therapy failure, complications and coronary aneurysms (CAAs), and this is the reason they deserve more aggressive therapy and a strict clinical follow-up. We report a 2-month-old male with KD, complicated by Macrophage Activation Syndrome (MAS). Despite timely and aggressive therapy with immunoglobulins, steroids and aspirin, multiple CAAs developed. Two-month therapy with anakinra completely reverted all the aneurysms. After six months, the infant experienced KD relapse and was successfully re-treated with immunoglobulins, steroids and aspirin. A strict echocardiographic follow-up did not show recurrence of aneurysms. Two years later, the child is healthy, without cardiac sequelae. In our experience, anakinra was effective in reverting multiple aneurysms and its effect proved to be long-lasting, even in front of KD recurrence. Based on this evidence, it seems reasonable to hypothesize not to limit the use of anakinra as rescue therapy for complicated or refractory KD, but to consider the possibility of adding it to first-line therapies for some subgroups of very-high-risk patients, in order to strengthen the prevention of CAAs.
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spelling pubmed-91391952022-05-28 Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome Bossi, Grazia Codazzi, Alessia Claudia Vinci, Federica Clerici, Edoardo Regalbuto, Corrado Crapanzano, Carmela Veraldi, Daniele Moiraghi, Alice Marseglia, Gian Luigi Children (Basel) Case Report Kawasaki disease (KD) is rare in infants less than 3 months of age, and its recurrence is exceptional. Infants with KD are at higher risk of severe clinical presentation, therapy failure, complications and coronary aneurysms (CAAs), and this is the reason they deserve more aggressive therapy and a strict clinical follow-up. We report a 2-month-old male with KD, complicated by Macrophage Activation Syndrome (MAS). Despite timely and aggressive therapy with immunoglobulins, steroids and aspirin, multiple CAAs developed. Two-month therapy with anakinra completely reverted all the aneurysms. After six months, the infant experienced KD relapse and was successfully re-treated with immunoglobulins, steroids and aspirin. A strict echocardiographic follow-up did not show recurrence of aneurysms. Two years later, the child is healthy, without cardiac sequelae. In our experience, anakinra was effective in reverting multiple aneurysms and its effect proved to be long-lasting, even in front of KD recurrence. Based on this evidence, it seems reasonable to hypothesize not to limit the use of anakinra as rescue therapy for complicated or refractory KD, but to consider the possibility of adding it to first-line therapies for some subgroups of very-high-risk patients, in order to strengthen the prevention of CAAs. MDPI 2022-05-05 /pmc/articles/PMC9139195/ /pubmed/35626849 http://dx.doi.org/10.3390/children9050672 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Bossi, Grazia
Codazzi, Alessia Claudia
Vinci, Federica
Clerici, Edoardo
Regalbuto, Corrado
Crapanzano, Carmela
Veraldi, Daniele
Moiraghi, Alice
Marseglia, Gian Luigi
Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title_full Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title_fullStr Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title_full_unstemmed Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title_short Efficacy of Anakinra on Multiple Coronary Arteries Aneurysms in an Infant with Recurrent Kawasaki Disease, Complicated by Macrophage Activation Syndrome
title_sort efficacy of anakinra on multiple coronary arteries aneurysms in an infant with recurrent kawasaki disease, complicated by macrophage activation syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139195/
https://www.ncbi.nlm.nih.gov/pubmed/35626849
http://dx.doi.org/10.3390/children9050672
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