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Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case

Kawasaki disease (KD) is a systemic vasculitis of unknown etiology and a leading cause of acquired heart disease. It is assumed that there is an activation of the immune system by an infectious trigger in a genetically susceptible host. Neuroblastoma is the most common extracranial solid tumor in yo...

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Autores principales: Alavi, Samin, Fahimzad, Alireza, Jadali, Farzaneh, Ghazizadeh, Farid, Rashidi, Armin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580901/
https://www.ncbi.nlm.nih.gov/pubmed/23476867
http://dx.doi.org/10.1155/2013/931703
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author Alavi, Samin
Fahimzad, Alireza
Jadali, Farzaneh
Ghazizadeh, Farid
Rashidi, Armin
author_facet Alavi, Samin
Fahimzad, Alireza
Jadali, Farzaneh
Ghazizadeh, Farid
Rashidi, Armin
author_sort Alavi, Samin
collection PubMed
description Kawasaki disease (KD) is a systemic vasculitis of unknown etiology and a leading cause of acquired heart disease. It is assumed that there is an activation of the immune system by an infectious trigger in a genetically susceptible host. Neuroblastoma is the most common extracranial solid tumor in young children. It mainly originates from primordial neural crest cells that generate the adrenal medulla and sympathetic ganglia. A diagnosis of concurrent KD and neuroblastoma in a living child has been made in only one previous report. We report the second case and review the literature.
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spelling pubmed-35809012013-03-09 Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case Alavi, Samin Fahimzad, Alireza Jadali, Farzaneh Ghazizadeh, Farid Rashidi, Armin Case Rep Pediatr Case Report Kawasaki disease (KD) is a systemic vasculitis of unknown etiology and a leading cause of acquired heart disease. It is assumed that there is an activation of the immune system by an infectious trigger in a genetically susceptible host. Neuroblastoma is the most common extracranial solid tumor in young children. It mainly originates from primordial neural crest cells that generate the adrenal medulla and sympathetic ganglia. A diagnosis of concurrent KD and neuroblastoma in a living child has been made in only one previous report. We report the second case and review the literature. Hindawi Publishing Corporation 2013 2013-02-06 /pmc/articles/PMC3580901/ /pubmed/23476867 http://dx.doi.org/10.1155/2013/931703 Text en Copyright © 2013 Samin Alavi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Alavi, Samin
Fahimzad, Alireza
Jadali, Farzaneh
Ghazizadeh, Farid
Rashidi, Armin
Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title_full Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title_fullStr Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title_full_unstemmed Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title_short Concurrent Adrenal Neuroblastoma and Kawasaki Disease: A Report of a Rare Case
title_sort concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580901/
https://www.ncbi.nlm.nih.gov/pubmed/23476867
http://dx.doi.org/10.1155/2013/931703
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