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Erschienen in: BMC Pulmonary Medicine 1/2014

Open Access 01.12.2014 | Research article

Comparative chest computed tomography findings of non-tuberculous mycobacterial lung diseases and pulmonary tuberculosis in patients with acid fast bacilli smear-positive sputum

verfasst von: Mei-Kang Yuan, Cheng-Yu Chang, Ping-Huang Tsai, Yuan-Ming Lee, Jen-Wu Huang, Shih-Chieh Chang

Erschienen in: BMC Pulmonary Medicine | Ausgabe 1/2014

Abstract

Background

Early diagnosis and treatment of nontuberculous mycobacterial lung diseases (NTM-LD) and pulmonary tuberculosis (PTB) are important clinical issues. The present study aimed to compare and identify the chest CT characteristics that help to distinguish NTM lung disease from PTB in patients with acid-fast bacilli (AFB) smear-positive sputum.

Methods

From January 2009 to April 2012, we received 467 AFB smear-positive sputum specimens. A total of 95 CT scans obtained from the 159 patients were analyzed, 75 scans were from patients with PTB and 20 scans from NTM-LD. The typical chest CT findings of mycobacterial diseases were analyzed.

Results

In patients with PTB, the prevalence of pleural effusion (38.7% vs. 15.0%; P =0.047), nodules < 10 mm in size (76.0% vs. 25.0%; P < 0.001), tree-in-bud pattern (81.3% vs. 55.0%; P =0.021), and cavities (31.1% vs. 5.0%; P =0.018) were significantly higher than patients with NTM. Of the 20 patients with NTM lung diseases, bronchiectasis and cystic changes were significantly higher than patients with PTB (20.0% vs. 4.0%; P = 0.034). In multivariate analysis, CT scan findings of nodules was independently associated with patients with diagnoses of PTB (odds ratio [OR], 0.07; 95% confidence interval [CI], 0.02-0.30). Presence of bronchiectasis and cystic changes in CT scans was strongly associated with patients with NTM-LD (OR, 33.04; 95% CI, 3.01-362.55).

Conclusions

The CT distinction between NTM-LD and PTB may help radiologists and physicians to know the most likely diagnoses in AFB-smear positive patients and avoid unnecessary adverse effects and the related costs of anti-TB drugs in endemic areas.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1471-2466-14-65) contains supplementary material, which is available to authorized users.
Mei-Kang Yuan, Cheng-Yu Chang contributed equally to this work.

Competing interests

The authors declare that they have no competing interests.

Authors’ contribution

MKY and CYC contributed equally to this work. MKY: study conception, design, and collection of data. CYC: drafting, submit and revise the manuscript. SCC: analysis and interpretation of data. PHT: study conception, design. Y-ML: acquisition and collection of data. JWH: acquisition and collection of data. All authors read and approved the final manuscript. All of the authors had access to the data and played a role in the writing this manuscript.

Background

The diagnosis and treatment of pulmonary diseases caused by mycobacterial infections are very important clinical issues. Among mycobacterial diseases, pulmonary tuberculosis (PTB) is the major entity and one of the world’s leading infectious diseases. In 2012, 8.6 million people felt ill with TB and 1.3 million died from TB [1]. Isolation of Mycobacterium tuberculosis from respiratory specimens is recommended for the definite diagnosis of PTB [2]. Microscopic examination of sputum smears for acid-fast bacilli (AFB) is widely used and the most efficient procedure for the initial screening of PTB. The presence of AFB in the stained sputum (AFB smear-positive) indicates a preliminary diagnosis of pulmonary mycobacterial infection. However, positive AFB smear test is not specific for PTB [35]. AFB smear-positive sputum may represent mycobacterium tuberculosis, but it can also represent non-tuberculous mycobacteria (NTM) [6]. NTM are ubiquitous organisms and its radiographic abnormalities and clinical symptoms changes slowly as compared with PTB [7]. In endemic areas, it is not uncommon to administer empirical anti-TB drugs in clinically suspected PTB patients with AFB smear-positive sputum. The isolation prevalence of NTM has increased gradually, which raise the concerns of unnecessary adverse effect and costs of anti-TB drugs [8, 9]. Therefore, additional diagnostic tools that help differentiate PTB and NTM is relevant in patients pending culture results. Radiological manifestations such as computed tomography (CT) features are useful to aid the diagnosis of PTB and NTM before definite mycobacterial culture because of its great availability and short examination time [10]. The aim of this study is to compare and identify the chest CT characteristics that help to distinguish NTM lung disease from PTB in patients with AFB smear-positive sputum.

Methods

Patients

From January 2009 to April 2012, we received 9,267 sputum specimens from 3,958 patients at the laboratory of National Yang-Ming University Hospital (a 512-bed regional teaching hospital in Yilan, Taiwan) and the Far Eastern Memorial Hospital (a 1050-bed tertiary medical center in Taipei, Taiwan). Of these sputum specimens, 467 from 236 patients were AFB stain-positive. Only 134 of the AFB stain-positive patients had proven pulmonary TB, and 25 patients proven NTM lung diseases. A total of 95 CT scans obtained from the 159 patients were analyzed, 75 scans were from patients with PTB and 20 scans from NTM lung disease. The study was approved by the Institutional Review Boards of the National Yang-Ming University Hospital and the Far Eastern Memorial Hospital. All participants gave written informed consent and agree of information collection in the study. All images of the participants were taken as part of standard patient care.

Diagnosis of pulmonary TB and NTM

All of the sputum specimens were treated with Ziehl-Neelsen staining. TB polymerase chain reaction (PCR) was performed with in-house IS6110-based PCR assays [11]. Mycobacterial cultures were performed using Löwenstein-Jensen medium [12]. Patients were diagnosed with pulmonary TB if M. tuberculosis was isolated from their sputum or tissue specimens. NTM was diagnosed according to mycobacterial cultures and the American Thoracic Society (ATS) guideline [13].

CT scanning methods

The CT scans were original films obtained from each institution. All CT examinations were performed within 3 months of AFB smear test. Conventional CT scans were performed with a 5 mm slice-thickness at 5 mm intervals by using multi-detector CT (Philips Brilliance 64). HRCT images were obtained with a 1 mm slice-thickness at 10 mm intervals. Scanning extended from the lung apices to below the costophrenic angles at maximum inspiration. The CT scans were reviewed independently by two experienced radiologists and pulmonary specialists blinded to the patient’s microbiology results. The final decisions regarding the findings were determined by consensus.

Statistical analysis

All statistical analyses were conducted using SPSS software for Windows (v 20; IBM Corporation, Armonk, NY, USA). Data are presented as frequencies for categorical variables, and by mean ± standard deviation for numerical variables. Categorical variables were compared using a chi-square test or Fisher’s exact test, and continuous variables were compared using an independent unpaired t-test. Univariate analysis was performed to evaluate the characteristic CT findings. Multivariate analysis was conducted using a logistic regression model to determine the independent predictive factors for patients with PTB and NTM infections. P-values of less than 0.05 were considered to be significant.

Results

The 75 patients with PTB included 58 men and 17 women with a mean age ± standard deviation of 65.6 years ±18.2 (range, 23–86 years). The 20 patients with NTM included 11 men and 9 women with a mean age ± standard deviation of 67.6 years ±14.6 (range, 30–92 years). The clinical data are summarized in Table 1. The CT findings were classified as presence or absence of pleural effusion, cavity formation, atelactasis, consolidation, nodules less than 10 mm in size, tree-in-bud pattern (branching centrilobular nodules), interlobular septal thickening, lung volume reduction, bronchiectasis, lymphadenopathy, calcified lymph nodes, as well as bronchiectasis and cystic changes. Of the 75 patients with PTB, 29 (38.7%) had pleural effusion vs. 3 (15.0%) in patients with NTM (P =0.047). 57 (76.0%) patients with PTB had nodules vs. 5 (25.0%) patients with NTM (P < 0.001). 61 (81.3%) patients with PTB had tree-in-bud opacities vs. 11 (55.0%) patients with NTM (P =0.021) (Figure 1). And 23 (31.1%) patients with PTB had cavities vs. 1 (5.0%) patient with NTM (P =0.018). Consalidation, lymphadenopathy and calcified lymph nodes were also more common in PTB patients. Of the 20 patients with NTM lung diseases, 4 (20.0%) had bronchiectasis and cystic changes vs. 3 (4.0%) patients with PTB; (P = 0.034) (Figures 2 and 3). Atelactasis, bronchiectasis without cystic changes and lung parenchymal volume reduction were more common in NTM lung diseases, but the univariate statistical results were not significant (Table 2). In multivariate analysis, CT scan findings of nodules was independently associated with patients with diagnoses of PTB (odds ratio [OR], 0.07; 95% confidence interval [CI], 0.02-0.30). Presence of bronchiectasis and cystic changes in CT scans was strongly associated with patients with NTM lung diseases (OR, 33.04; 95% CI, 3.01-362.55) (Table 3).
Table 1
Clinical characteristics of patients with pulmonary tuberculosis and NTM lung diseases
 
Pulmonary tuberculosis n = 75
NTM lung disease n = 20
Pvalue
Age, years
65.57 ± 18.20
67.60 ± 14.63
0.647
Male
58 (77.3)
11 (55.0)
0.047
Ever smoker
24 (32.0)
3 (15.0)
0.134
Diabetes mellitus
14 (18.7)
3 (15.0)
1.000
Malignancy
3 (4.0)
0 (0.0)
1.000
Autoimmune disease
2 (2.7)
1 (5.0)
0.512
COPD
9 (12.0)
4 (20.0)
0.463
Pneumoconiosis
1 (1.3)
1 (5.0)
0.378
Numbers in parentheses are percentages. NTM: non-tuberculosis mycobacterium; COPD: chronic obstructive pulmonary disease.
Table 2
Comparative chest CT findings of non-tuberculous mycobacterial lung diseases and pulmonary tuberculosis
 
Pulmonary tuberculosis n = 75
NTM lung diseases n = 20
Pvalue
Chest CT findings
  
Pleural effusion
29 (38.7)
3 (15.0)
0.047
Cavities
23 (31.1)
1 (5.0)
0.018
Atelectasis
41 (54.7)
12 (60.0)
0.670
Consolidation
41 (54.7)
9 (45.0)
0.442
Random nodules
57 (76.0)
5 (25.0)
<0.001
Interlobular septal thickening
67 (89.3)
17 (85.0)
0.694
Bronchiectasis
10 (13.3)
4 (20.0)
0.484
Lung volume reduction
7 (9.3)
4 (20.0)
0.236
Tree-in-bud pattern
61 (81.3)
11 (55.0)
0.021
Lymphadenopathy
18 (24.0)
1 (5.0)
0.066
Calcified lymph nodes
5 (6.7)
0 (0.0)
0.580
Bronchiectasis and cystic changes
3 (4.0)
4 (20.0)
0.034
Numbers in parentheses are percentages. NTM = non-tuberculous mycobacterium.
CT = computed tomography.
Table 3
Multivariate analysis of predictors for NTM lung diseases
CT findings
Odds ratio
95% CI
  
Bronchiectasis and cystic changes
33.035
3.010-362.552
Favor NTM
 
Pleural effusion
0.198
0.038-1.031
Favor PTB
 
Random nodules
0.074
0.019-0.296
Favor PTB
 
CI = confidence interval; PTB = pulmonary tuberculosis; NTM = nontuberculous mycobacterium.

Discussion

The present study shows that chest CT findings could help to differentiate pulmonary TB from NTM lung diseases. Upon comparing CT features between PTB and NTM, pleural effusion, nodules are significantly more common in patients with PTB and bronchiectasis combined with cystic changes are significantly more common in patients with NTM infections. In multivariate analysis, presence of nodules is significantly associated with PTB, and bronchiectasis combined with cystic changes are strongly associated with NTM lung diseases.
The definite diagnosis of PTB still depends on PCR or mycobacterial culture from bronchial washing or sputum. Clinical symptoms and image findings also play an important role in the diagnosis of TB. Typical radiological features of pulmonary TB include parenchymal diseases such as consolidation and cavities; pleural effusion, variable-sized nodules and lymphadenopathy are well documented and repeatedly reviewed in literatures. The CT findings in our study are mostly identical to the previously reported radiological findings of PTB. Familiar thin-section chest CT findings of nontuberculous mycobacterial infection include bronchiectasis, small and large nodules, centrilobular nodules, consolidation and fibrocavitary lesions [14, 15]. Our study also demonstrates the common radiographic findings of bronchiectasis, tree-in-bud pattern, atelactasis and consolidation in patients with NTM lung diseases, but there are no significant differences as compared with the PTB patients. To our knowledge, the CT finding of bronchiectasis and cystic changes in NTM infection has not been emphasized in the previous studies. Although the radiological evidence of severe bronchiectasis and subsequent cystic changes, which is traditionally described as the honeycomb appearance, usually represents end-stage interstitial fibrosis, it is reported to be a dynamic process and may have different evolution [16, 17]. In order to exclude the pre-existing bronchiectasis and cystic changes, the previous films of the four patients with NTM lung diseases demonstrating bronchiectasis and cystic changes were reviewed since the PACS implementation in our institutions from March 2004. Regarding the diagnosis of NTM, the isolation of NTM species from a respiratory sample is an insufficient evidence for the definite diagnosis of NTM lung disease. Some patients with positive NTM culture do not have evidences of pulmonary disease, and such infection may indicate colonization or transient infection. Therefore, the ATS issued diagnostic criteria for NTM lung diseases which not only rely on microbiological examinations, the clinical and radiographic evidences are also essential. Clinical researches have shown that disease attributable to NTM has a rising trend in many developed and developing countries [18, 19]. In endemic areas, immediate and empirical treatment of mycobacterial diseases based on the result of AFB sputum smear has an important impact on disease transmission control. However, the administration of unnecessary empiric anti-TB treatment is not uncommon in real world practice and patients might suffer from the adverse effects of anti-TB drugs. Our colleagues (Shih-Chieh Chang, et al.) issued an article that revealed 40.4% of patients with positive sputum AFB stains did not have pulmonary TB in Taiwan [20]. According to Chang’s results, among patients who had positive sputum AFB stains without pulmonary TB, 25.8% were prescribed anti-TB treatment and 44% of them developed various adverse effects (hepatitis: 32%; skin rash: 20%). Although the adverse effects were usually not lethal, however, they did cause unnecessary harm. Our study provides radiographic evidence that chest CT finding of the bronchiectasis and cystic changes is statistically a strong indicator of NTM disease in patients with AFB smear-positive sputum. This characteristic CT feature is helpful to distinguish NTM from PTB in patients with equivocal clinical symptoms and pending culture results. Considering our results, physicians can make more precise decisions to initiate empiric anti-TB treatment and avoid unnecessary adverse effects on patients with final diagnoses of NTM lung diseases.
Our study had several limitations that are worth noting. Not all the AFB smear-positive patients with NTM lung diseases underwent chest CT. It was likely that the study was biased toward patients with severe infection who warranted further CT scans evaluation. In all cases, CT scans were obtained within 3 months of AFB smear tests. Some AFB smear-positive patients had received empirical anti-TB drugs. The CT findings in patients with actual PTB diagnoses might show improvement and somewhat not identical to the typical features of pulmonary TB. Finally, although there was a strong association of random nodules in PTB as well as bronchiectasis and cystic changes in NTM-LD statistically, the conclusions drawn by our statistical results needed a large-scale analysis to be confirmed.

Conclusions

Our results suggest that pulmonary tuberculosis and NTM lung diseases can usually be distinguished by assessing the CT findings of nodules in patients with PTB as well as bronchiectasis and cystic changes with NTM. The CT distinction between these two mycobacterial infections may help radiologists and physicians to know the most likely diagnoses in AFB-smear positive patients and avoid unnecessary adverse effects and costs of anti-TB drugs in endemic areas.
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://​creativecommons.​org/​licenses/​by/​2.​0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

The authors declare that they have no competing interests.

Authors’ contribution

MKY and CYC contributed equally to this work. MKY: study conception, design, and collection of data. CYC: drafting, submit and revise the manuscript. SCC: analysis and interpretation of data. PHT: study conception, design. Y-ML: acquisition and collection of data. JWH: acquisition and collection of data. All authors read and approved the final manuscript. All of the authors had access to the data and played a role in the writing this manuscript.
Literatur
2.
Zurück zum Zitat Blumberg HM, Burman WJ, Chaisson RE, Daley CL, Etkind SC, Friedman LN, Fujiwara P, Grzemska M, Hopewell PC, Iseman MD, Jasmer RM, Koppaka V, Menzies RI, O’Brien RJ, Reves RR, Reichman LB, Simone PM, Starke JR, Vernon AA, American Thoracic Society, Centers for Disease Control and Prevention and the Infectious Diseases Society: American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: treatment of tuberculosis. Am J Respir Crit Care Med. 2003, 167: 603-662.CrossRefPubMed Blumberg HM, Burman WJ, Chaisson RE, Daley CL, Etkind SC, Friedman LN, Fujiwara P, Grzemska M, Hopewell PC, Iseman MD, Jasmer RM, Koppaka V, Menzies RI, O’Brien RJ, Reves RR, Reichman LB, Simone PM, Starke JR, Vernon AA, American Thoracic Society, Centers for Disease Control and Prevention and the Infectious Diseases Society: American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: treatment of tuberculosis. Am J Respir Crit Care Med. 2003, 167: 603-662.CrossRefPubMed
4.
Zurück zum Zitat Tuberculosis Division, International Union against Tuberculosis and Lung Disease: Tuberculosis bacteriology-priorities and indications in high prevalence countries: position of the technical staff of the tuberculosis division of the International Union against Tuberculosis and Lung Disease. Int J Tuberc Lung Dis. 2005, 9: 355-361. Tuberculosis Division, International Union against Tuberculosis and Lung Disease: Tuberculosis bacteriology-priorities and indications in high prevalence countries: position of the technical staff of the tuberculosis division of the International Union against Tuberculosis and Lung Disease. Int J Tuberc Lung Dis. 2005, 9: 355-361.
5.
Zurück zum Zitat Maiga M, Siddiqui S, Diallo S, Diarra B, Traoré B, Shea YR, Zelazny AM, Dembele BP, Goita D, Kassambara H, Hammond AS, Polis MA, Tounkara A: Failure to recognize nontuberculous mycobacteria leads to misdiagnosis of chronic pulmonary tuberculosis. PLoS One. 2012, 7: e36902-10.1371/journal.pone.0036902.CrossRefPubMedPubMedCentral Maiga M, Siddiqui S, Diallo S, Diarra B, Traoré B, Shea YR, Zelazny AM, Dembele BP, Goita D, Kassambara H, Hammond AS, Polis MA, Tounkara A: Failure to recognize nontuberculous mycobacteria leads to misdiagnosis of chronic pulmonary tuberculosis. PLoS One. 2012, 7: e36902-10.1371/journal.pone.0036902.CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat American Thoracic Society: Diagnostic standards and classification of tuberculosis in adults and children. Am J Respir Crit Care Med. 2000, 161: 1376-1395.CrossRef American Thoracic Society: Diagnostic standards and classification of tuberculosis in adults and children. Am J Respir Crit Care Med. 2000, 161: 1376-1395.CrossRef
7.
Zurück zum Zitat Woodring JH, Vandiviere HM: Pulmonary disease caused by nontuberculous mycobacteria. J Thorac Imaging. 1990, 5: 64-76. 10.1097/00005382-199004000-00009.CrossRefPubMed Woodring JH, Vandiviere HM: Pulmonary disease caused by nontuberculous mycobacteria. J Thorac Imaging. 1990, 5: 64-76. 10.1097/00005382-199004000-00009.CrossRefPubMed
8.
Zurück zum Zitat Marras TK, Daley CL: Epidemiology of human pulmonary infection with nontuberculous mycobacteria. Clin Chest Med. 2002, 23: 553-567. 10.1016/S0272-5231(02)00019-9.CrossRefPubMed Marras TK, Daley CL: Epidemiology of human pulmonary infection with nontuberculous mycobacteria. Clin Chest Med. 2002, 23: 553-567. 10.1016/S0272-5231(02)00019-9.CrossRefPubMed
9.
Zurück zum Zitat Marras TK, Chedore P, Ying AM, Jamieson F: Isolation prevalence of pulmonary non-tuberculous mycobacteria in Ontario, 1997–2003. Thorax. 2007, 62: 661-666. 10.1136/thx.2006.070797.CrossRefPubMedPubMedCentral Marras TK, Chedore P, Ying AM, Jamieson F: Isolation prevalence of pulmonary non-tuberculous mycobacteria in Ontario, 1997–2003. Thorax. 2007, 62: 661-666. 10.1136/thx.2006.070797.CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Jeong YJ, Lee KS, Koh WJ, Han J, Kim TS, Kwon OJ: Nontuberculous mycobacterial pulmonary infection in immunocompetent patients: comparison of thin-section CT and histopathologic findings. Radiology. 2004, 231: 880-886. 10.1148/radiol.2313030833.CrossRefPubMed Jeong YJ, Lee KS, Koh WJ, Han J, Kim TS, Kwon OJ: Nontuberculous mycobacterial pulmonary infection in immunocompetent patients: comparison of thin-section CT and histopathologic findings. Radiology. 2004, 231: 880-886. 10.1148/radiol.2313030833.CrossRefPubMed
11.
Zurück zum Zitat Sun JR, Lee SY, Perng CL, Lu JJ: Detecting mycobacterium tuberculosis in bactec MGIT 960 cultures by inhouse IS6110-based PCR assay in routine clinical practice. J Formos Med Assoc. 2009, 108: 119-125. 10.1016/S0929-6646(09)60042-5.CrossRefPubMed Sun JR, Lee SY, Perng CL, Lu JJ: Detecting mycobacterium tuberculosis in bactec MGIT 960 cultures by inhouse IS6110-based PCR assay in routine clinical practice. J Formos Med Assoc. 2009, 108: 119-125. 10.1016/S0929-6646(09)60042-5.CrossRefPubMed
12.
Zurück zum Zitat Tarshis MS, Kinsella PC, Parker MV, Blood media for the cultivation of Mycobacterium tuberculosis: VII: Comparison of blood agar-penicillin and lowenstein-jensen media under routine diagnostic conditions. J Bacteriol. 1953, 66: 448-452.PubMedPubMedCentral Tarshis MS, Kinsella PC, Parker MV, Blood media for the cultivation of Mycobacterium tuberculosis: VII: Comparison of blood agar-penicillin and lowenstein-jensen media under routine diagnostic conditions. J Bacteriol. 1953, 66: 448-452.PubMedPubMedCentral
13.
Zurück zum Zitat Diagnosis and treatment of disease caused by nontuberculous mycobacteria: This official statement of the American Thoracic Society was approved by the Board of Directors, March 1997. Medical section of the American Lung Association. Am J Respir Crit Care Med. 1997, 156: S1-S25.CrossRef Diagnosis and treatment of disease caused by nontuberculous mycobacteria: This official statement of the American Thoracic Society was approved by the Board of Directors, March 1997. Medical section of the American Lung Association. Am J Respir Crit Care Med. 1997, 156: S1-S25.CrossRef
14.
Zurück zum Zitat Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, Holland SM, Horsburgh R, Huitt G, Iademarco MF, Iseman M, Olivier K, Ruoss S, von Reyn CF, Wallace RJ, Winthrop K, ATS Mycobacterial Diseases Subcommittee; American Thoracic Society; Infectious Disease Society of America: An official ATS/IDSA statement: diagnosis, treatment, and prevention of non-tuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007, 175: 367-416. 10.1164/rccm.200604-571ST.CrossRefPubMed Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, Holland SM, Horsburgh R, Huitt G, Iademarco MF, Iseman M, Olivier K, Ruoss S, von Reyn CF, Wallace RJ, Winthrop K, ATS Mycobacterial Diseases Subcommittee; American Thoracic Society; Infectious Disease Society of America: An official ATS/IDSA statement: diagnosis, treatment, and prevention of non-tuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007, 175: 367-416. 10.1164/rccm.200604-571ST.CrossRefPubMed
15.
Zurück zum Zitat Hollings NP, Wells AU, Wilson R, Hansell DM: Comparative appearances of non-tuberculous mycobacteria species: a CT study. Eur Radiol. 2002, 12: 2211-2217.CrossRefPubMed Hollings NP, Wells AU, Wilson R, Hansell DM: Comparative appearances of non-tuberculous mycobacteria species: a CT study. Eur Radiol. 2002, 12: 2211-2217.CrossRefPubMed
16.
Zurück zum Zitat Lee HY, Lee KS, Jeong YJ, Hwang JH, Kim HJ, Chung MP, Han J: High-resolution CT findings in fibrotic idiopathic interstitial pneumonias with little honeycombing: serial changes and prognostic implications. AJR Am J Roentgenol. 2012, 199: 982-989. 10.2214/AJR.11.8192.CrossRefPubMed Lee HY, Lee KS, Jeong YJ, Hwang JH, Kim HJ, Chung MP, Han J: High-resolution CT findings in fibrotic idiopathic interstitial pneumonias with little honeycombing: serial changes and prognostic implications. AJR Am J Roentgenol. 2012, 199: 982-989. 10.2214/AJR.11.8192.CrossRefPubMed
17.
Zurück zum Zitat Mineo G, Ciccarese F, Attinà D, Di Scioscio V, Sciascia N, Bono L, Rocca A, Stella F, Zompatori M: Natural history of honeycombing: follow-up of patients with idiopathic pulmonary fibrosis treated with single-lung transplantation. Radiol Med. 2013, 118: 40-50. 10.1007/s11547-012-0810-4.CrossRefPubMed Mineo G, Ciccarese F, Attinà D, Di Scioscio V, Sciascia N, Bono L, Rocca A, Stella F, Zompatori M: Natural history of honeycombing: follow-up of patients with idiopathic pulmonary fibrosis treated with single-lung transplantation. Radiol Med. 2013, 118: 40-50. 10.1007/s11547-012-0810-4.CrossRefPubMed
18.
Zurück zum Zitat Fowler SJ, French J, Screaton NJ, Foweraker J, Condliffe A, Haworth CS, Exley AR, Bilton D: Nontuberculous mycobacteria in bronchiectasis: prevalence and patient characteristics. Eur Respir J. 2006, 28: 1204-1210. 10.1183/09031936.06.00149805.CrossRefPubMed Fowler SJ, French J, Screaton NJ, Foweraker J, Condliffe A, Haworth CS, Exley AR, Bilton D: Nontuberculous mycobacteria in bronchiectasis: prevalence and patient characteristics. Eur Respir J. 2006, 28: 1204-1210. 10.1183/09031936.06.00149805.CrossRefPubMed
19.
Zurück zum Zitat Dailloux M, Abalain ML, Laurain C, Lebrun L, Loos-Ayav C, Lozniewski A, Maugein J, French Mycobacteria Study Group: Respiratory infections associated with nontuberculous mycobacteria in non-HIV patients. Eur Respir J. 2006, 28: 1211-1215. 10.1183/09031936.00063806.CrossRefPubMed Dailloux M, Abalain ML, Laurain C, Lebrun L, Loos-Ayav C, Lozniewski A, Maugein J, French Mycobacteria Study Group: Respiratory infections associated with nontuberculous mycobacteria in non-HIV patients. Eur Respir J. 2006, 28: 1211-1215. 10.1183/09031936.00063806.CrossRefPubMed
20.
Zurück zum Zitat Chang CY, Hong JY, Yuan MK, Chang SJ, Lee YM, Chang SC, Hsu LC, Cheng SL: Risk factors in AFB smear-positive patients who receive inappropriate antituberculous treatment. Drug Des Devel Ther. 2013, 7: 53-58.CrossRefPubMedPubMedCentral Chang CY, Hong JY, Yuan MK, Chang SJ, Lee YM, Chang SC, Hsu LC, Cheng SL: Risk factors in AFB smear-positive patients who receive inappropriate antituberculous treatment. Drug Des Devel Ther. 2013, 7: 53-58.CrossRefPubMedPubMedCentral
Metadaten
Titel
Comparative chest computed tomography findings of non-tuberculous mycobacterial lung diseases and pulmonary tuberculosis in patients with acid fast bacilli smear-positive sputum
verfasst von
Mei-Kang Yuan
Cheng-Yu Chang
Ping-Huang Tsai
Yuan-Ming Lee
Jen-Wu Huang
Shih-Chieh Chang
Publikationsdatum
01.12.2014
Verlag
BioMed Central
Erschienen in
BMC Pulmonary Medicine / Ausgabe 1/2014
Elektronische ISSN: 1471-2466
DOI
https://doi.org/10.1186/1471-2466-14-65

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