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Published in: BMC Infectious Diseases 1/2019

Open Access 01-12-2019 | Tuberculosis | Research article

Comparison of pleural effusion features and biomarkers between talaromycosis and tuberculosis in non-human immunodeficiency virus-infected patients

Authors: Ye Qiu, Wen Zeng, Hui Zhang, Xiaoning Zhong, Shudan Tang, Jianquan Zhang

Published in: BMC Infectious Diseases | Issue 1/2019

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Abstract

Background

Due to the similar clinical, lung imaging, and pathological characteristics, talaromycosis is most commonly misdiagnosed as tuberculosis. This study aimed to identify the characteristics of talaromycosis pleural effusion (TMPE) and to distinguish TMPE from tuberculosis pleural effusion (TPE).

Methods

We enrolled 19 cases each of TMPE and TPE from Guangxi, China. Patients’ clinical records, pleural effusion tests, biomarker test results, and receiver operating characteristic curves were analyzed.

Results

In total, 39.8% (65/163) of patients exhibited serous effusion, of whom 61 were non-human immunodeficiency virus (HIV)-infected patients; 68.85% of the non-HIV-infected patients (42/61) had TMPE. Thoracentesis was performed only in 19 patients, all of whom were misdiagnosed with tuberculosis and received long-term anti-tuberculosis treatment. In four of these patients, interleukin (IL)-23, IL-27, and interferon-gamma (IFN-γ) measurements were not performed since pleural effusion samples could not be collected because the effusion had been drained prior to the study. In the remaining 15 patients, pleural effusion samples were collected. Talaromyces marneffei was isolated from the pleural effusion and pleural nodules. Most TMPEs were characterized by yellowish fluid, with marked elevation of protein content and nucleated cell counts. However, neutrophils were predominantly found in TMPEs, and lymphocytes were predominantly found in TPEs (both p < 0.05). Adenosine deaminase (ADA) and IFN-γ levels in TMPEs were significantly lower than those in TPEs (all p < 0.05) and provided similar accuracies for distinguishing TMPEs from TPEs. IL-23 concentration in TMPEs was significantly higher than that in TPEs (p < 0.05), and it provided similar accuracy for diagnosing TMPEs. IL-27 concentrations in TMPEs were significantly lower than those in TPEs (all p < 0.05) but was not useful for distinguishing TMPE from TPE.

Conclusions

Talaromycosis can infringe on the pleural cavity via the translocation of T. marneffei into the pleural space. Nonetheless, this phenomenon is still commonly neglected by clinicians. TMPE is a yellowish fluid with exudative PEs and predominant neutrophils. Higher neutrophil counts and IL-23 may suggest talaromycosis. Higher lymphocyte counts, ADA activity, and IFN-γ concentration may suggest tuberculosis.
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Literature
1.
go back to reference Le T, Kinh NV, Cuc NT, Tung NL, Lam NT, Thuy PT, et al. A trial of Itraconazole or amphotericin B for HIV-associated Talaromycosis. N Engl J Med. 2017;376:2329–40.CrossRef Le T, Kinh NV, Cuc NT, Tung NL, Lam NT, Thuy PT, et al. A trial of Itraconazole or amphotericin B for HIV-associated Talaromycosis. N Engl J Med. 2017;376:2329–40.CrossRef
2.
go back to reference Li Q, Wang C, Zeng K, Peng X, Wang F. AIDS-associated disseminated talaromycosis (penicilliosis) marneffei. J Dtsch Dermatol Ges. 2018;16:1256–9.PubMed Li Q, Wang C, Zeng K, Peng X, Wang F. AIDS-associated disseminated talaromycosis (penicilliosis) marneffei. J Dtsch Dermatol Ges. 2018;16:1256–9.PubMed
3.
go back to reference Wang YF, Xu HF, Han ZG, Zeng L, Liang CY, Chen XJ, et al. Serological surveillance for Penicillium marneffei infection in HIV-infected patients during 2004-2011 in Guangzhou. China Clin Microbiol Infect. 2015;21:484–9.CrossRef Wang YF, Xu HF, Han ZG, Zeng L, Liang CY, Chen XJ, et al. Serological surveillance for Penicillium marneffei infection in HIV-infected patients during 2004-2011 in Guangzhou. China Clin Microbiol Infect. 2015;21:484–9.CrossRef
4.
go back to reference Chan JF, Lau SK, Yuen KY, Woo PC. Talaromyces (Penicillium) marneffei infection in non-HIV-infected patients. Emerg Microbes Infect. 2016;5:e19.PubMedPubMedCentral Chan JF, Lau SK, Yuen KY, Woo PC. Talaromyces (Penicillium) marneffei infection in non-HIV-infected patients. Emerg Microbes Infect. 2016;5:e19.PubMedPubMedCentral
5.
go back to reference Qiu Y, Pan M, Zhang J, Zhong X, Li Y, Zhang H, et al. Two unusual cases of human immunodeficiency virus-negative patients with Talaromyces marneffei infection. Am J Trop Med Hyg. 2016;95:426–30.CrossRef Qiu Y, Pan M, Zhang J, Zhong X, Li Y, Zhang H, et al. Two unusual cases of human immunodeficiency virus-negative patients with Talaromyces marneffei infection. Am J Trop Med Hyg. 2016;95:426–30.CrossRef
6.
go back to reference Qiu Y, Zhang J, Liu G, Zhong X, Deng J, He Z, et al. A case of Penicillium marneffei infection involving the main tracheal structure. BMC Infect Dis. 2014;14:242.CrossRef Qiu Y, Zhang J, Liu G, Zhong X, Deng J, He Z, et al. A case of Penicillium marneffei infection involving the main tracheal structure. BMC Infect Dis. 2014;14:242.CrossRef
7.
go back to reference Kawila R, Chaiwarith R, Supparatpinyo K. Clinical and laboratory characteristics of penicilliosis marneffei among patients with and without HIV infection in northern Thailand: a retrospective study. BMC Infect Dis. 2013;13:464.CrossRef Kawila R, Chaiwarith R, Supparatpinyo K. Clinical and laboratory characteristics of penicilliosis marneffei among patients with and without HIV infection in northern Thailand: a retrospective study. BMC Infect Dis. 2013;13:464.CrossRef
8.
go back to reference Porcel JM, Azzopardi M, Koegelenberg CF, Maldonado F, Rahman NM, Lee YC. The diagnosis of pleural effusions. Expert Rev Respir Med. 2015;9:801–15.CrossRef Porcel JM, Azzopardi M, Koegelenberg CF, Maldonado F, Rahman NM, Lee YC. The diagnosis of pleural effusions. Expert Rev Respir Med. 2015;9:801–15.CrossRef
9.
go back to reference Ferreiro L, Sánchez-Sánchez R, Valdés L, Kummerfeldt CE, Huggins JT. Concordant and discordant exudates and their effect on the accuracy of Light's criteria to diagnose exudative pleural effusions. Am J Med Sci. 2016;352:549–56.CrossRef Ferreiro L, Sánchez-Sánchez R, Valdés L, Kummerfeldt CE, Huggins JT. Concordant and discordant exudates and their effect on the accuracy of Light's criteria to diagnose exudative pleural effusions. Am J Med Sci. 2016;352:549–56.CrossRef
10.
go back to reference McGrath EE, Anderson PB. Diagnosis of pleural effusion: a systematic approach. Am J Crit Care. 2011;20:119–27.CrossRef McGrath EE, Anderson PB. Diagnosis of pleural effusion: a systematic approach. Am J Crit Care. 2011;20:119–27.CrossRef
11.
go back to reference Wang W, Zhou Q, Zhai K, Wang Y, Liu JY, Wang XJ, et al. Diagnostic accuracy of interleukin 27 for tuberculous pleural effusion: two prospective studies and one meta-analysis. Thorax. 2018;73:240–7.CrossRef Wang W, Zhou Q, Zhai K, Wang Y, Liu JY, Wang XJ, et al. Diagnostic accuracy of interleukin 27 for tuberculous pleural effusion: two prospective studies and one meta-analysis. Thorax. 2018;73:240–7.CrossRef
12.
go back to reference Gopi A, Madhavan SM, Sharma SK, Sahn SA. Diagnosis and treatment of tuberculous pleural effusion in 2006. Chest. 2007;131:880–9.CrossRef Gopi A, Madhavan SM, Sharma SK, Sahn SA. Diagnosis and treatment of tuberculous pleural effusion in 2006. Chest. 2007;131:880–9.CrossRef
13.
go back to reference Zweig MH, Campbell G. Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine. Clin Chem. 1993;39:561–77. Zweig MH, Campbell G. Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine. Clin Chem. 1993;39:561–77.
14.
go back to reference Hanley JA, McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148:839–43.CrossRef Hanley JA, McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148:839–43.CrossRef
15.
go back to reference Qiu Y, Zhang J, Liu G, Zhong X, Deng J, He Z, et al. Retrospective analysis of 14 cases of disseminated Penicillium marneffei infection with osteolytic lesions. BMC Infect Dis. 2015;15:47.CrossRef Qiu Y, Zhang J, Liu G, Zhong X, Deng J, He Z, et al. Retrospective analysis of 14 cases of disseminated Penicillium marneffei infection with osteolytic lesions. BMC Infect Dis. 2015;15:47.CrossRef
16.
go back to reference Qiu Y, Liao H, Zhang J, Zhong X, Tan C, Lu D. Differences in clinical characteristics and prognosis of Penicilliosis among HIV-negative patients with or without underlying disease in southern China: a retrospective study. BMC Infect Dis. 2015;15:525.CrossRef Qiu Y, Liao H, Zhang J, Zhong X, Tan C, Lu D. Differences in clinical characteristics and prognosis of Penicilliosis among HIV-negative patients with or without underlying disease in southern China: a retrospective study. BMC Infect Dis. 2015;15:525.CrossRef
17.
go back to reference Skouras VS, Kalomenidis I. Pleural fluid tests to diagnose tuberculous pleuritis. Curr Opin Pulm Med. 2016;22:367–77.CrossRef Skouras VS, Kalomenidis I. Pleural fluid tests to diagnose tuberculous pleuritis. Curr Opin Pulm Med. 2016;22:367–77.CrossRef
18.
go back to reference Devkota KC, Shyam BK, Sherpa K, Ghimire P, Sherpa MT, Shrestha R, et al. Significance of adenosine deaminase in diagnosing tuberculous pleural effusion. Nepal Med Coll J. 2012;14:149–52.PubMed Devkota KC, Shyam BK, Sherpa K, Ghimire P, Sherpa MT, Shrestha R, et al. Significance of adenosine deaminase in diagnosing tuberculous pleural effusion. Nepal Med Coll J. 2012;14:149–52.PubMed
19.
go back to reference Kelchtermans H, Billiau A, Matthys P. How interferon-gamma keeps autoimmune diseases in check. Trends Immunol. 2008;29:479–86.CrossRef Kelchtermans H, Billiau A, Matthys P. How interferon-gamma keeps autoimmune diseases in check. Trends Immunol. 2008;29:479–86.CrossRef
20.
go back to reference Hu X, Ivashkiv LB. Cross-regulation of signaling pathways by interferon-gamma: implications for immune responses and autoimmune diseases. Immunity. 2009;31:539–50.CrossRef Hu X, Ivashkiv LB. Cross-regulation of signaling pathways by interferon-gamma: implications for immune responses and autoimmune diseases. Immunity. 2009;31:539–50.CrossRef
21.
go back to reference Browne SK, Burbelo PD, Chetchotisakd P, Suputtamongkol Y, Kiertiburanakul S, Shaw PA, et al. Adult-onset immunodeficiency in Thailand and Taiwan. N Engl J Med. 2012;367:725–34.CrossRef Browne SK, Burbelo PD, Chetchotisakd P, Suputtamongkol Y, Kiertiburanakul S, Shaw PA, et al. Adult-onset immunodeficiency in Thailand and Taiwan. N Engl J Med. 2012;367:725–34.CrossRef
22.
go back to reference Miossec P, Korn T, Kuchroo VK. Interleukin-17 and type 17 helper T cells. N Engl J Med. 2009;361:888–98.CrossRef Miossec P, Korn T, Kuchroo VK. Interleukin-17 and type 17 helper T cells. N Engl J Med. 2009;361:888–98.CrossRef
23.
go back to reference Zeng N, Wan C, Qin J, Wu Y, Yang T, Shen Y, et al. Diagnostic value of interleukins for tuberculous pleural effusion: a systematic review and meta-analysis. BMC Pulm Med. 2017;17:180.CrossRef Zeng N, Wan C, Qin J, Wu Y, Yang T, Shen Y, et al. Diagnostic value of interleukins for tuberculous pleural effusion: a systematic review and meta-analysis. BMC Pulm Med. 2017;17:180.CrossRef
Metadata
Title
Comparison of pleural effusion features and biomarkers between talaromycosis and tuberculosis in non-human immunodeficiency virus-infected patients
Authors
Ye Qiu
Wen Zeng
Hui Zhang
Xiaoning Zhong
Shudan Tang
Jianquan Zhang
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2019
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-019-4376-6

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