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Kawasaki Disease Presenting as Acute Acalculous Cholecystitis

Acute acalculous cholecystitis (AAC) is a rare, potentially serious disease that has been associated with Kawasaki disease (KD) in children. Studies suggest that patients presenting with severe abdominal symptoms secondary to KD have increased resistance to intravenous immunoglobulin (IVIG), and a h...

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Detalles Bibliográficos
Autores principales: Lipe, Demis N., Bridges, Lindsey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861022/
https://www.ncbi.nlm.nih.gov/pubmed/31763594
http://dx.doi.org/10.5811/cpcem.2019.8.44255
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author Lipe, Demis N.
Bridges, Lindsey C.
author_facet Lipe, Demis N.
Bridges, Lindsey C.
author_sort Lipe, Demis N.
collection PubMed
description Acute acalculous cholecystitis (AAC) is a rare, potentially serious disease that has been associated with Kawasaki disease (KD) in children. Studies suggest that patients presenting with severe abdominal symptoms secondary to KD have increased resistance to intravenous immunoglobulin (IVIG), and a higher rate of coronary artery aneurysms. We describe an eight-year-old boy who presented to the emergency department with severe abdominal pain and was diagnosed with AAC and KD. He was treated with IVIG and high-dose aspirin, achieving good response with complete symptom resolution. He had no coronary artery aneurysms or further complications and was discharged after three days.
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spelling pubmed-68610222019-11-22 Kawasaki Disease Presenting as Acute Acalculous Cholecystitis Lipe, Demis N. Bridges, Lindsey C. Clin Pract Cases Emerg Med Case Report Acute acalculous cholecystitis (AAC) is a rare, potentially serious disease that has been associated with Kawasaki disease (KD) in children. Studies suggest that patients presenting with severe abdominal symptoms secondary to KD have increased resistance to intravenous immunoglobulin (IVIG), and a higher rate of coronary artery aneurysms. We describe an eight-year-old boy who presented to the emergency department with severe abdominal pain and was diagnosed with AAC and KD. He was treated with IVIG and high-dose aspirin, achieving good response with complete symptom resolution. He had no coronary artery aneurysms or further complications and was discharged after three days. University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2019-10-14 /pmc/articles/PMC6861022/ /pubmed/31763594 http://dx.doi.org/10.5811/cpcem.2019.8.44255 Text en Copyright: © 2019 Lipe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) License. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Case Report
Lipe, Demis N.
Bridges, Lindsey C.
Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title_full Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title_fullStr Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title_full_unstemmed Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title_short Kawasaki Disease Presenting as Acute Acalculous Cholecystitis
title_sort kawasaki disease presenting as acute acalculous cholecystitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861022/
https://www.ncbi.nlm.nih.gov/pubmed/31763594
http://dx.doi.org/10.5811/cpcem.2019.8.44255
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