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Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease

In China, tuberculosis (TB) is endemic and the Bacillus Callmette–Güerin (BCG) vaccine is administered to all the newborns, which may lead to BCG infection in patients with chronic granulomatous disease (CGD). Infection of BCG/TB in CGD patients can be fatal and pulmonary is the most affected organ....

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Autores principales: Yao, Qiong, Zhou, Qin-hua, Shen, Quan-li, Wang, Xiao-chuan, Hu, Xi-hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273607/
https://www.ncbi.nlm.nih.gov/pubmed/35817807
http://dx.doi.org/10.1038/s41598-022-16021-9
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author Yao, Qiong
Zhou, Qin-hua
Shen, Quan-li
Wang, Xiao-chuan
Hu, Xi-hong
author_facet Yao, Qiong
Zhou, Qin-hua
Shen, Quan-li
Wang, Xiao-chuan
Hu, Xi-hong
author_sort Yao, Qiong
collection PubMed
description In China, tuberculosis (TB) is endemic and the Bacillus Callmette–Güerin (BCG) vaccine is administered to all the newborns, which may lead to BCG infection in patients with chronic granulomatous disease (CGD). Infection of BCG/TB in CGD patients can be fatal and pulmonary is the most affected organ. Our objective was to assess the imaging of pulmonary BCG/TB infection in CGD. We screened 169 CGD patients and identified the patients with pulmonary BCG/TB infection. BCG infection was diagnosis according to the vaccination history, local infection manifestation, acid-fast bacilli staining, specific polymerase chain reaction, and/or spoligotyping. PPD, T-SPOT and acid-fast bacilli staining were used for diagnosis of TB. Totally 58 patients were identified, including TB (n = 7), solely BCG (n = 18), BCG + bacterial (n = 20), and BCG + fungi (n = 13). The onset of BCG disease was much earlier than TB. For those patients only with BCG, lymphadenopathy was the first and most prevalent feature. The most found location was the left axilla, followed by the ipsilateral cervical areas and mediastinal or hilar area. On chest CT, ground-glass opacities, multiple nodules and pulmonary scarring were the most common findings. For TB patients, the pulmonary infections were more serious, including large masses, severe lymphadenopathy, and extensive pulmonary fibrosis. Pulmonary infection of BCG were more common than TB in CGD patients, but much less severe.
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spelling pubmed-92736072022-07-13 Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease Yao, Qiong Zhou, Qin-hua Shen, Quan-li Wang, Xiao-chuan Hu, Xi-hong Sci Rep Article In China, tuberculosis (TB) is endemic and the Bacillus Callmette–Güerin (BCG) vaccine is administered to all the newborns, which may lead to BCG infection in patients with chronic granulomatous disease (CGD). Infection of BCG/TB in CGD patients can be fatal and pulmonary is the most affected organ. Our objective was to assess the imaging of pulmonary BCG/TB infection in CGD. We screened 169 CGD patients and identified the patients with pulmonary BCG/TB infection. BCG infection was diagnosis according to the vaccination history, local infection manifestation, acid-fast bacilli staining, specific polymerase chain reaction, and/or spoligotyping. PPD, T-SPOT and acid-fast bacilli staining were used for diagnosis of TB. Totally 58 patients were identified, including TB (n = 7), solely BCG (n = 18), BCG + bacterial (n = 20), and BCG + fungi (n = 13). The onset of BCG disease was much earlier than TB. For those patients only with BCG, lymphadenopathy was the first and most prevalent feature. The most found location was the left axilla, followed by the ipsilateral cervical areas and mediastinal or hilar area. On chest CT, ground-glass opacities, multiple nodules and pulmonary scarring were the most common findings. For TB patients, the pulmonary infections were more serious, including large masses, severe lymphadenopathy, and extensive pulmonary fibrosis. Pulmonary infection of BCG were more common than TB in CGD patients, but much less severe. Nature Publishing Group UK 2022-07-11 /pmc/articles/PMC9273607/ /pubmed/35817807 http://dx.doi.org/10.1038/s41598-022-16021-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yao, Qiong
Zhou, Qin-hua
Shen, Quan-li
Wang, Xiao-chuan
Hu, Xi-hong
Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title_full Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title_fullStr Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title_full_unstemmed Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title_short Imaging characteristics of pulmonary BCG/TB infection in patients with chronic granulomatous disease
title_sort imaging characteristics of pulmonary bcg/tb infection in patients with chronic granulomatous disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273607/
https://www.ncbi.nlm.nih.gov/pubmed/35817807
http://dx.doi.org/10.1038/s41598-022-16021-9
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