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Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014

During a 2014 measles outbreak in Vietnam, postmortem pathologic examination of hospitalized children who died showed that adenovirus type 7 pneumonia was a contributory cause of death in children with measles-associated immune suppression. Adenovirus type 7 pneumonia should be recognized as a major...

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Autores principales: Hai, Le Thanh, Thach, Hoang Ngoc, Tuan, Ta Anh, Nam, Dao Huu, Dien, Tran Minh, Sato, Yuko, Kumasaka, Toshio, Suzuki, Tadaki, Hanaoka, Nozomu, Fujimoto, Tsuguto, Katano, Harutaka, Hasegawa, Hideki, Kawachi, Shoji, Nakajima, Noriko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806935/
https://www.ncbi.nlm.nih.gov/pubmed/26926035
http://dx.doi.org/10.3201/eid2204.151595
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author Hai, Le Thanh
Thach, Hoang Ngoc
Tuan, Ta Anh
Nam, Dao Huu
Dien, Tran Minh
Sato, Yuko
Kumasaka, Toshio
Suzuki, Tadaki
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katano, Harutaka
Hasegawa, Hideki
Kawachi, Shoji
Nakajima, Noriko
author_facet Hai, Le Thanh
Thach, Hoang Ngoc
Tuan, Ta Anh
Nam, Dao Huu
Dien, Tran Minh
Sato, Yuko
Kumasaka, Toshio
Suzuki, Tadaki
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katano, Harutaka
Hasegawa, Hideki
Kawachi, Shoji
Nakajima, Noriko
author_sort Hai, Le Thanh
collection PubMed
description During a 2014 measles outbreak in Vietnam, postmortem pathologic examination of hospitalized children who died showed that adenovirus type 7 pneumonia was a contributory cause of death in children with measles-associated immune suppression. Adenovirus type 7 pneumonia should be recognized as a major cause of secondary infection after measles.
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spelling pubmed-48069352016-04-01 Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014 Hai, Le Thanh Thach, Hoang Ngoc Tuan, Ta Anh Nam, Dao Huu Dien, Tran Minh Sato, Yuko Kumasaka, Toshio Suzuki, Tadaki Hanaoka, Nozomu Fujimoto, Tsuguto Katano, Harutaka Hasegawa, Hideki Kawachi, Shoji Nakajima, Noriko Emerg Infect Dis Dispatch During a 2014 measles outbreak in Vietnam, postmortem pathologic examination of hospitalized children who died showed that adenovirus type 7 pneumonia was a contributory cause of death in children with measles-associated immune suppression. Adenovirus type 7 pneumonia should be recognized as a major cause of secondary infection after measles. Centers for Disease Control and Prevention 2016-04 /pmc/articles/PMC4806935/ /pubmed/26926035 http://dx.doi.org/10.3201/eid2204.151595 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Dispatch
Hai, Le Thanh
Thach, Hoang Ngoc
Tuan, Ta Anh
Nam, Dao Huu
Dien, Tran Minh
Sato, Yuko
Kumasaka, Toshio
Suzuki, Tadaki
Hanaoka, Nozomu
Fujimoto, Tsuguto
Katano, Harutaka
Hasegawa, Hideki
Kawachi, Shoji
Nakajima, Noriko
Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title_full Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title_fullStr Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title_full_unstemmed Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title_short Adenovirus Type 7 Pneumonia in Children Who Died from Measles-Associated Pneumonia, Hanoi, Vietnam, 2014
title_sort adenovirus type 7 pneumonia in children who died from measles-associated pneumonia, hanoi, vietnam, 2014
topic Dispatch
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806935/
https://www.ncbi.nlm.nih.gov/pubmed/26926035
http://dx.doi.org/10.3201/eid2204.151595
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