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Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia

BACKGROUND: M. pneumoniae pneumonia (MP) has been reported in 10-40% of community-acquired pneumonia cases. We aimed to evaluate the difference of clinical features in children with MP, according to their age and chest radiographic patterns. METHODS: The diagnosis of MP was made by examinations at b...

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Autores principales: Youn, You-Sook, Lee, Kyung-Yil, Hwang, Ja-Young, Rhim, Jung-Woo, Kang, Jin-Han, Lee, Joon-Sung, Kim, Ji-Chang
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910686/
https://www.ncbi.nlm.nih.gov/pubmed/20604923
http://dx.doi.org/10.1186/1471-2431-10-48
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author Youn, You-Sook
Lee, Kyung-Yil
Hwang, Ja-Young
Rhim, Jung-Woo
Kang, Jin-Han
Lee, Joon-Sung
Kim, Ji-Chang
author_facet Youn, You-Sook
Lee, Kyung-Yil
Hwang, Ja-Young
Rhim, Jung-Woo
Kang, Jin-Han
Lee, Joon-Sung
Kim, Ji-Chang
author_sort Youn, You-Sook
collection PubMed
description BACKGROUND: M. pneumoniae pneumonia (MP) has been reported in 10-40% of community-acquired pneumonia cases. We aimed to evaluate the difference of clinical features in children with MP, according to their age and chest radiographic patterns. METHODS: The diagnosis of MP was made by examinations at both admission and discharge and by two serologic tests: the indirect microparticle agglutinin assay (≥1:40) and the cold agglutinins titer (≥1:32). A total of 191 children with MP were grouped by age: ≤2 years of age (29 patients), 3-5 years of age (81 patients), and ≥6 years of age (81 patients). They were also grouped by pneumonia pattern: bronchopneumonia group (96 patients) and segmental/lobar pneumonia group (95 patients). RESULTS: Eighty-six patients (45%) were seroconverters, and the others showed increased antibody titers during hospitalization. Among the three age groups, the oldest children showed the longest duration of fever, highest C-reactive protein (CRP) values, and the most severe pneumonia pattern. The patients with segmental/lobar pneumonia were older and had longer fever duration and lower white blood cell (WBC) and lymphocyte counts, compared with those with bronchopneumonia. The patient group with the most severe pulmonary lesions had the most prolonged fever, highest CRP, highest rate of seroconverters, and lowest lymphocyte counts. Thrombocytosis was observed in 8% of patients at admission, but in 33% of patients at discharge. CONCLUSIONS: In MP, older children had more prolonged fever and more severe pulmonary lesions. The severity of pulmonary lesions was associated with the absence of diagnostic IgM antibodies at presentation and lymphocyte count. Short-term paired IgM serologic test may be mandatory for early and definitive diagnosis of MP.
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spelling pubmed-29106862010-07-28 Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia Youn, You-Sook Lee, Kyung-Yil Hwang, Ja-Young Rhim, Jung-Woo Kang, Jin-Han Lee, Joon-Sung Kim, Ji-Chang BMC Pediatr Research Article BACKGROUND: M. pneumoniae pneumonia (MP) has been reported in 10-40% of community-acquired pneumonia cases. We aimed to evaluate the difference of clinical features in children with MP, according to their age and chest radiographic patterns. METHODS: The diagnosis of MP was made by examinations at both admission and discharge and by two serologic tests: the indirect microparticle agglutinin assay (≥1:40) and the cold agglutinins titer (≥1:32). A total of 191 children with MP were grouped by age: ≤2 years of age (29 patients), 3-5 years of age (81 patients), and ≥6 years of age (81 patients). They were also grouped by pneumonia pattern: bronchopneumonia group (96 patients) and segmental/lobar pneumonia group (95 patients). RESULTS: Eighty-six patients (45%) were seroconverters, and the others showed increased antibody titers during hospitalization. Among the three age groups, the oldest children showed the longest duration of fever, highest C-reactive protein (CRP) values, and the most severe pneumonia pattern. The patients with segmental/lobar pneumonia were older and had longer fever duration and lower white blood cell (WBC) and lymphocyte counts, compared with those with bronchopneumonia. The patient group with the most severe pulmonary lesions had the most prolonged fever, highest CRP, highest rate of seroconverters, and lowest lymphocyte counts. Thrombocytosis was observed in 8% of patients at admission, but in 33% of patients at discharge. CONCLUSIONS: In MP, older children had more prolonged fever and more severe pulmonary lesions. The severity of pulmonary lesions was associated with the absence of diagnostic IgM antibodies at presentation and lymphocyte count. Short-term paired IgM serologic test may be mandatory for early and definitive diagnosis of MP. BioMed Central 2010-07-06 /pmc/articles/PMC2910686/ /pubmed/20604923 http://dx.doi.org/10.1186/1471-2431-10-48 Text en Copyright ©2010 Youn et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Youn, You-Sook
Lee, Kyung-Yil
Hwang, Ja-Young
Rhim, Jung-Woo
Kang, Jin-Han
Lee, Joon-Sung
Kim, Ji-Chang
Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title_full Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title_fullStr Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title_full_unstemmed Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title_short Difference of clinical features in childhood Mycoplasma pneumoniae pneumonia
title_sort difference of clinical features in childhood mycoplasma pneumoniae pneumonia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910686/
https://www.ncbi.nlm.nih.gov/pubmed/20604923
http://dx.doi.org/10.1186/1471-2431-10-48
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