Talaromyces marneffei infection and complicate manifestation of respiratory system in HIV-negative children

Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, a...

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Published inBMC pulmonary medicine Vol. 23; no. 1; pp. 100 - 10
Main Authors Yang, Qin, Wu, Yue, Li, Xiaonan, Bao, Yanmin, Wang, Wenjian, Zheng, Yuejie
Format Journal Article
LanguageEnglish
Published London BioMed Central 28.03.2023
BioMed Central Ltd
BMC
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ISSN1471-2466
1471-2466
DOI10.1186/s12890-023-02390-y

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Abstract Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. Methods We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. Results All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii , which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. Conclusion The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
AbstractList Abstract Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. Methods We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. Results All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. Conclusion The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of [beta]-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment.BACKGROUNDRespiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment.We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation.METHODSWe retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation.All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months.RESULTSAll subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months.The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.CONCLUSIONThe first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. Methods We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. Results All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii , which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. Conclusion The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
BackgroundRespiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment.MethodsWe retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation.ResultsAll subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of β-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months.ConclusionThe first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important.
Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early identification of TM infection in human immunodeficiency virus (HIV)-negative children with respiratory symptoms as the first manifestation, analyze the risk factors, and provide evidence for diagnosis and treatment. Methods We retrospectively analyzed six cases of HIV-negative children with respiratory system infection symptoms as the first presentation. Results All subjects (100%) had cough and hepatosplenomegaly, and five subjects (83.3%) had a fever; other symptoms and signs included lymph node enlargement, rash, rales, wheezing, hoarseness, hemoptysis, anemia, and thrush. Additionally, 66.7% of the cases had underlying diseases (three had malnutrition, one had severe combined immune deficiency [SCID]). The most common coinfecting pathogen was Pneumocystis jirovecii, which occurred in two cases (33.3%), followed by one case of Aspergillus sp. (16.6%). Furthermore, the value of [beta]-D-glucan detection (G test) increased in 50% of the cases, while the proportion of NK decreased in six cases (100%). Five children (83.3%) were confirmed to have the pathogenic genetic mutations. Three children (50%) were treated with amphotericin B, voriconazole, and itraconazole, respectively; three children (50%) were treated with voriconazole and itraconazole. All children were tested for itraconazole and voriconazole plasma concentrations throughout antifungal therapy. Two cases (33.3%) relapsed after drug withdrawal within 1 year, and the average duration of antifungal treatment for all children was 17.7 months. Conclusion The first manifestation of TM infection in children is respiratory symptoms, which are nonspecific and easily misdiagnosed. When the effectiveness of anti-infection treatment is poor for recurrent respiratory tract infections, we must consider the condition with an opportunistic pathogen and attempt to identify the pathogen using various samples and detection methods to confirm the diagnosis. It is recommended the course for anti-TM disease be longer than one year for children with immune deficiency. Monitoring the blood concentration of antifungal drugs is important. Keywords: Talaromyces marneffei, Respiratory system, Children, Antifungal therapy
ArticleNumber 100
Audience Academic
Author Yang, Qin
Li, Xiaonan
Bao, Yanmin
Wang, Wenjian
Wu, Yue
Zheng, Yuejie
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  organization: Department of Clinical Pharmacy, Shenzhen Children’s Hospital, Shantou University Medical College
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  organization: Department of Respiratory Diseases, Shenzhen Children’s Hospital, Shantou University Medical College
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CitedBy_id crossref_primary_10_3389_fimmu_2025_1492000
crossref_primary_10_3390_jof11020158
crossref_primary_10_1093_mmy_myae094
Cites_doi 10.1093/mmy/myx004
10.4155/fsoa-2017-0032
10.3389/fimmu.2021.654406
10.1016/j.ccm.2017.04.008
10.1093/cid/cir754
10.1128/IAI.00679-18
10.1097/MD.0000000000001439
10.1186/1471-2334-13-464
10.1007/s11046-022-00659-0
10.1016/j.clim.2020.108553
10.1007/s11046-016-0107-3
10.2147/IDR.S232713
10.1084/jem.20110958
10.1093/jac/dkt508
10.1111/myc.13295
10.21037/apm-20-2056
10.1186/s12879-021-05978-z
10.1007/s11046-021-00570-0
10.1186/s12887-021-03100-5
10.1186/s12879-019-4376-6
10.1186/s12887-022-03726-z
10.3390/pathogens11121465
10.3389/fcimb.2022.851891
10.1038/emi.2016.18
10.4269/ajtmh.20-0909
10.1016/j.jmii.2020.02.007
10.1007/BF01103897
10.1007/s11046-017-0236-3
10.1016/S2213-2600(18)30345-X
10.1177/0300060520959484
10.1371/journal.ppat.1005400
10.1038/s41598-020-78178-5
10.3390/jof8020200
10.1007/s40265-013-0069-4
10.1093/cid/cir028
10.1016/j.jaci.2013.08.051
10.1093/ofid/ofz205
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Issue 1
Keywords Antifungal therapy
Respiratory system
Children
Talaromyces marneffei
Language English
License 2023. The Author(s).
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References YG Wang (2390_CR38) 2018; 183
L He (2390_CR1) 2021; 64
Q Lang (2390_CR2) 2020; 104
Y Ouyang (2390_CR41) 2017; 182
K Pruksaphon (2390_CR26) 2020; 10
RJ Wang (2390_CR18) 2017; 38
RJ Hamill (2390_CR39) 2013; 73
MS Lionakis (2390_CR33) 2023; 4
R Kawila (2390_CR19) 2013; 13
F Hu (2390_CR29) 2021; 54
D Cheng (2390_CR15) 2020; 48
S Narayanasamy (2390_CR11) 2021; 186
2390_CR4
D Abd Elaziz (2390_CR40) 2020; 219
JH Fan (2390_CR5) 2021; 10
H Fan (2390_CR34) 2022; 22
L Liu (2390_CR32) 2011; 208
W Zhang (2390_CR31) 2021; 12
PL White (2390_CR8) 2017; 55
PPW Lee (2390_CR37) 2014; 133
HR Ashbee (2390_CR9) 2014; 69
WH Lam (2390_CR28) 2019; 87
K Pruksaphon (2390_CR12) 2022; 8
JFW Chan (2390_CR3) 2016; 5
GM Gregory (2390_CR10) 2017; 2017
M Pan (2390_CR21) 2019; 12
L Ajello (2390_CR23) 1995; 131
RJ Dong (2390_CR27) 2019; 6
F Shu (2390_CR25) 2022; 11
PPW Lee (2390_CR6) 2012; 54
M Pongpom (2390_CR24) 2017; 3
E Azoulay (2390_CR30) 2019; 7
Y Qiu (2390_CR22) 2019; 19
W Hu (2390_CR14) 2022; 22
Y Zhan (2390_CR17) 2022; 12
T Le (2390_CR13) 2011; 52
Q Zeng (2390_CR20) 2021; 21
X Wang (2390_CR7) 2016; 12
W Zeng (2390_CR16) 2015; 94
L Wang (2390_CR36) 2022; 187
F Cossu (2390_CR35) 2010; 36
References_xml – volume: 55
  start-page: 843
  year: 2017
  ident: 2390_CR8
  publication-title: Med Mycol
  doi: 10.1093/mmy/myx004
– volume: 3
  start-page: FSO215
  year: 2017
  ident: 2390_CR24
  publication-title: Future Sci OA
  doi: 10.4155/fsoa-2017-0032
– volume: 12
  start-page: 654406
  year: 2021
  ident: 2390_CR31
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2021.654406
– ident: 2390_CR4
– volume: 38
  start-page: 465
  year: 2017
  ident: 2390_CR18
  publication-title: Clin Chest Med
  doi: 10.1016/j.ccm.2017.04.008
– volume: 54
  start-page: e8
  year: 2012
  ident: 2390_CR6
  publication-title: Clin Infect Dis
  doi: 10.1093/cid/cir754
– volume: 87
  start-page: e00679
  year: 2019
  ident: 2390_CR28
  publication-title: Infect Immun
  doi: 10.1128/IAI.00679-18
– volume: 94
  start-page: e1439
  year: 2015
  ident: 2390_CR16
  publication-title: Med (Baltim)
  doi: 10.1097/MD.0000000000001439
– volume: 13
  start-page: 464
  year: 2013
  ident: 2390_CR19
  publication-title: BMC Infect Dis
  doi: 10.1186/1471-2334-13-464
– volume: 187
  start-page: 455
  year: 2022
  ident: 2390_CR36
  publication-title: Mycopathologia
  doi: 10.1007/s11046-022-00659-0
– volume: 219
  start-page: 108553
  year: 2020
  ident: 2390_CR40
  publication-title: Clin Immunol
  doi: 10.1016/j.clim.2020.108553
– volume: 182
  start-page: 569
  year: 2017
  ident: 2390_CR41
  publication-title: Mycopathologia
  doi: 10.1007/s11046-016-0107-3
– volume: 12
  start-page: 3807
  year: 2019
  ident: 2390_CR21
  publication-title: Infect Drug Resist
  doi: 10.2147/IDR.S232713
– volume: 208
  start-page: 1635
  year: 2011
  ident: 2390_CR32
  publication-title: J Exp Med
  doi: 10.1084/jem.20110958
– volume: 69
  start-page: 1162
  year: 2014
  ident: 2390_CR9
  publication-title: J Antimicrob Chemother
  doi: 10.1093/jac/dkt508
– volume: 64
  start-page: 1170
  year: 2021
  ident: 2390_CR1
  publication-title: Mycoses
  doi: 10.1111/myc.13295
– volume: 10
  start-page: 8437
  year: 2021
  ident: 2390_CR5
  publication-title: Ann Palliat Med
  doi: 10.21037/apm-20-2056
– volume: 21
  start-page: 287
  year: 2021
  ident: 2390_CR20
  publication-title: BMC Infect Dis
  doi: 10.1186/s12879-021-05978-z
– volume: 186
  start-page: 707
  year: 2021
  ident: 2390_CR11
  publication-title: Mycopathologia
  doi: 10.1007/s11046-021-00570-0
– volume: 22
  start-page: 28
  year: 2022
  ident: 2390_CR14
  publication-title: BMC Pediatr
  doi: 10.1186/s12887-021-03100-5
– volume: 19
  start-page: 745
  year: 2019
  ident: 2390_CR22
  publication-title: BMC Infect Dis
  doi: 10.1186/s12879-019-4376-6
– volume: 22
  start-page: 675
  issue: 1
  year: 2022
  ident: 2390_CR34
  publication-title: BMC Pediatr
  doi: 10.1186/s12887-022-03726-z
– volume: 11
  start-page: 1465
  year: 2022
  ident: 2390_CR25
  publication-title: Pathogens
  doi: 10.3390/pathogens11121465
– volume: 12
  start-page: 851891
  year: 2022
  ident: 2390_CR17
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2022.851891
– volume: 5
  start-page: e19
  year: 2016
  ident: 2390_CR3
  publication-title: Emerg Microbes Infect
  doi: 10.1038/emi.2016.18
– volume: 104
  start-page: 744
  year: 2020
  ident: 2390_CR2
  publication-title: Am J Trop Med Hyg
  doi: 10.4269/ajtmh.20-0909
– volume: 54
  start-page: 457
  year: 2021
  ident: 2390_CR29
  publication-title: J Microbiol Immunol Infect
  doi: 10.1016/j.jmii.2020.02.007
– volume: 131
  start-page: 1
  year: 1995
  ident: 2390_CR23
  publication-title: Mycopathologia
  doi: 10.1007/BF01103897
– volume: 183
  start-page: 551
  year: 2018
  ident: 2390_CR38
  publication-title: Mycopathologia
  doi: 10.1007/s11046-017-0236-3
– volume: 7
  start-page: 173
  year: 2019
  ident: 2390_CR30
  publication-title: Lancet Respir Med
  doi: 10.1016/S2213-2600(18)30345-X
– volume: 48
  start-page: 300060520959484
  year: 2020
  ident: 2390_CR15
  publication-title: J Int Med Res
  doi: 10.1177/0300060520959484
– volume: 12
  start-page: e1005400
  year: 2016
  ident: 2390_CR7
  publication-title: PLoS Pathog
  doi: 10.1371/journal.ppat.1005400
– volume: 10
  start-page: 21169
  year: 2020
  ident: 2390_CR26
  publication-title: Sci Rep
  doi: 10.1038/s41598-020-78178-5
– volume: 8
  start-page: 200
  year: 2022
  ident: 2390_CR12
  publication-title: J Fungi (Basel)
  doi: 10.3390/jof8020200
– volume: 73
  start-page: 919
  year: 2013
  ident: 2390_CR39
  publication-title: Drugs
  doi: 10.1007/s40265-013-0069-4
– volume: 52
  start-page: 945
  year: 2011
  ident: 2390_CR13
  publication-title: Clin Infect Dis
  doi: 10.1093/cid/cir028
– volume: 2017
  start-page: 8491383
  year: 2017
  ident: 2390_CR10
  publication-title: Mediators Inflamm
– volume: 36
  start-page: 76
  year: 2010
  ident: 2390_CR35
  publication-title: J Pediatr
– volume: 133
  start-page: 894
  year: 2014
  ident: 2390_CR37
  publication-title: J Allergy Clin Immunol
  doi: 10.1016/j.jaci.2013.08.051
– volume: 4
  start-page: 1
  year: 2023
  ident: 2390_CR33
  publication-title: Nat Rev Immunol
– volume: 6
  start-page: ofz205
  year: 2019
  ident: 2390_CR27
  publication-title: Open Forum Infect Dis
  doi: 10.1093/ofid/ofz205
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Snippet Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early...
Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early...
Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early...
BackgroundRespiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve the early...
Abstract Background Respiratory symptoms are the earliest clinical manifestation of Talaromyces marneffei (TM) infection. In this study, we aimed to improve...
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SubjectTerms AIDS-Related Opportunistic Infections - diagnosis
Amphotericin B
Antifungal agents
Antifungal Agents - therapeutic use
Antifungal therapy
Blood levels
Bone marrow
Care and treatment
Causes of
Child
Children
Cough
Critical Care Medicine
Diagnosis
Disease
Dosage and administration
Fever
Genomes
Health aspects
Hemoptysis
HIV
HIV infection in children
Hospitals
Human immunodeficiency virus
Humans
Hyperthermia
Immunosuppressive agents
Infections
Intensive
Internal Medicine
Itraconazole
Itraconazole - therapeutic use
Lymph nodes
Lymphatic system
Malnutrition
Medicine
Medicine & Public Health
Morphology
Mortality
Opportunist infection
Pathogens
Patients
Plasma
Pneumology/Respiratory System
Prevention
Pulmonology
Recurrent infection
Respiratory System
Respiratory tract diseases
Respiratory Tract Infections - complications
Respiratory Tract Infections - diagnosis
Respiratory Tract Infections - drug therapy
Retrospective Studies
Risk factors
Talaromyces
Talaromyces marneffei
Voriconazole
Voriconazole - therapeutic use
Wheezing
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Title Talaromyces marneffei infection and complicate manifestation of respiratory system in HIV-negative children
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