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Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report

BACKGROUND: The etiology of Kawasaki disease (KD) remains unknown. However, many studies have suggested that specific genetic factors and/or some infectious agents underlie the onset of KD. Previous studies have suggested that human adenovirus (HAdV) is one of the triggering pathogens of KD. Here, w...

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Autores principales: Fukuda, Sayaka, Ito, Shuichi, Fujiwara, Maya, Abe, Jun, Hanaoka, Nozomu, Fujimoto, Tsuguto, Katsumori, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432973/
https://www.ncbi.nlm.nih.gov/pubmed/28511718
http://dx.doi.org/10.1186/s12969-017-0169-x
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author Fukuda, Sayaka
Ito, Shuichi
Fujiwara, Maya
Abe, Jun
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katsumori, Hiroshi
author_facet Fukuda, Sayaka
Ito, Shuichi
Fujiwara, Maya
Abe, Jun
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katsumori, Hiroshi
author_sort Fukuda, Sayaka
collection PubMed
description BACKGROUND: The etiology of Kawasaki disease (KD) remains unknown. However, many studies have suggested that specific genetic factors and/or some infectious agents underlie the onset of KD. Previous studies have suggested that human adenovirus (HAdV) is one of the triggering pathogens of KD. Here, we report monozygotic twin boys who sequentially developed KD in conjunction with acute HAdV type 3 (HAdV-3) infection. CASE PRESENTATION: The patients were four-year-old monozygotic twin boys. The elder brother developed a high fever and was diagnosed with HAdV infection with an immunochromatographic kit for HAdV (IC-kit). He was transferred to our institute after persistent fever for 7 days. On admission, he already fulfilled all the diagnostic criteria for KD. His laboratory data were as follows: WBC, 9700/μl; CRP, 2.42 mg/dl; IFN-γ, 99.8 pg/ml; and TNF-α, 10.9 pg/ml. He received intravenous immunoglobulin (IVIG) and aspirin and responded well, with no coronary artery abnormalities. The younger brother, who was also IC-kit-positive, was hospitalized on the same day as his elder brother after persistent fever for 3 days. His data on admission were as follows: WBC, 12,600/μl; CRP, 5.54 mg/dl; IFN-γ, 105.0 pg/ml; and TNF-α, 33.6 pg/ml. Although he developed all of the typical KD symptoms by day 4, his fever subsided spontaneously on day 6 without IVIG or aspirin. However, he developed a dilation of the coronary artery in the region of the left circumflex artery bifurcation on day 10. His coronary artery dilation had resolved 3 months after onset. HAdV-3 DNA was detected with PCR in stool samples from both patients, and HAdV3 was isolated from the younger brother’s stool sample. Serum neutralizing antibodies to AdV3 were also significantly elevated in both patients, suggesting seroconversion. CONCLUSIONS: There have been few reports of the simultaneous development of KD in monozygotic twins. Notably, both twins had an acute HAdV-3 infection immediately before they developed KD. These cases strongly suggest that KD was triggered by HAdV-3 infection, and they indicate that specific immune responses to some pathogens (such as HAdV-3), arising from genetic susceptibility, play a critical role in the pathogenesis of KD.
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spelling pubmed-54329732017-05-17 Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report Fukuda, Sayaka Ito, Shuichi Fujiwara, Maya Abe, Jun Hanaoka, Nozomu Fujimoto, Tsuguto Katsumori, Hiroshi Pediatr Rheumatol Online J Case Report BACKGROUND: The etiology of Kawasaki disease (KD) remains unknown. However, many studies have suggested that specific genetic factors and/or some infectious agents underlie the onset of KD. Previous studies have suggested that human adenovirus (HAdV) is one of the triggering pathogens of KD. Here, we report monozygotic twin boys who sequentially developed KD in conjunction with acute HAdV type 3 (HAdV-3) infection. CASE PRESENTATION: The patients were four-year-old monozygotic twin boys. The elder brother developed a high fever and was diagnosed with HAdV infection with an immunochromatographic kit for HAdV (IC-kit). He was transferred to our institute after persistent fever for 7 days. On admission, he already fulfilled all the diagnostic criteria for KD. His laboratory data were as follows: WBC, 9700/μl; CRP, 2.42 mg/dl; IFN-γ, 99.8 pg/ml; and TNF-α, 10.9 pg/ml. He received intravenous immunoglobulin (IVIG) and aspirin and responded well, with no coronary artery abnormalities. The younger brother, who was also IC-kit-positive, was hospitalized on the same day as his elder brother after persistent fever for 3 days. His data on admission were as follows: WBC, 12,600/μl; CRP, 5.54 mg/dl; IFN-γ, 105.0 pg/ml; and TNF-α, 33.6 pg/ml. Although he developed all of the typical KD symptoms by day 4, his fever subsided spontaneously on day 6 without IVIG or aspirin. However, he developed a dilation of the coronary artery in the region of the left circumflex artery bifurcation on day 10. His coronary artery dilation had resolved 3 months after onset. HAdV-3 DNA was detected with PCR in stool samples from both patients, and HAdV3 was isolated from the younger brother’s stool sample. Serum neutralizing antibodies to AdV3 were also significantly elevated in both patients, suggesting seroconversion. CONCLUSIONS: There have been few reports of the simultaneous development of KD in monozygotic twins. Notably, both twins had an acute HAdV-3 infection immediately before they developed KD. These cases strongly suggest that KD was triggered by HAdV-3 infection, and they indicate that specific immune responses to some pathogens (such as HAdV-3), arising from genetic susceptibility, play a critical role in the pathogenesis of KD. BioMed Central 2017-05-16 /pmc/articles/PMC5432973/ /pubmed/28511718 http://dx.doi.org/10.1186/s12969-017-0169-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Case Report
Fukuda, Sayaka
Ito, Shuichi
Fujiwara, Maya
Abe, Jun
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katsumori, Hiroshi
Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title_full Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title_fullStr Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title_full_unstemmed Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title_short Simultaneous development of Kawasaki disease following acute human adenovirus infection in monozygotic twins: A case report
title_sort simultaneous development of kawasaki disease following acute human adenovirus infection in monozygotic twins: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432973/
https://www.ncbi.nlm.nih.gov/pubmed/28511718
http://dx.doi.org/10.1186/s12969-017-0169-x
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