- Research article
- Open Access
- Open Peer Review
Detection of Pulmonary tuberculosis: comparing MR imaging with HRCT
© Rizzi et al; licensee BioMed Central Ltd. 2011
- Received: 11 August 2010
- Accepted: 16 September 2011
- Published: 16 September 2011
Computer Tomography (CT) is considered the gold standard for assessing the morphological changes of lung parenchyma. Although novel CT techniques have substantially decreased the radiation dose, radiation exposure is still high. Magnetic Resonance Imaging (MRI) has been established as a radiation- free alternative to CT for several lung diseases, but its role in infectious diseases still needs to be explored further. Therefore, the purpose of our study was to compare MRI with high resolution CT (HRCT) for assessing pulmonary tuberculosis.
50 patients with culture-proven pulmonary tuberculosis underwent chest HRCT as the standard of reference and were evaluated by MRI within 24 h after HRCT. Altogether we performed 60 CT and MRI examinations, because 10 patients were also examined by CT and MRI at follow- up. Pulmonary abnormalities, their characteristics, location and distribution were analyzed by two readers who were blinded to the HRCT results.
Artifacts did not interfere with the diagnostic value of MRI. Both HRCT and MRI correctly diagnosed pulmonary tuberculosis and identified pulmonary abnormalities in all patients. There were no significant differences between the two techniques in terms of identifying the location and distribution of the lung lesions, though the higher resolution of MRI did allow for better identification of parenchymal dishomogeneity, caseosis, and pleural or nodal involvement.
Technical developments and the refinement of pulse sequences have improved the quality and speed of MRI. Our data indicate that in terms of identifying lung lesions in non-AIDS patients with non- miliary pulmonary tuberculosis, MRI achieves diagnostic performances comparable to those obtained by HRCT but with better and more rapid identification of pulmonary tissue abnormalities due to the excellent contrast resolution.
- Magnetic Resonance Image
- Computer Tomography
- Pulmonary Tuberculosis
- Magnetic Resonance Image Feature
- Interstitial Change
CT is considered the gold standard for assessing the morphological changes of lung parenchyma. Although novel CT techniques have substantially decreased the radiation dose, radiation exposure is still high. Magnetic Resonance Imaging (MRI) has been established as a radiation- free alternative to CT for several lung diseases, explaining the growing interest in (MRI) for lung parenchyma. New technologies and strategies which allow for very fast imaging and improved image quality [1, 2] have been introduced, but their role in infectious diseases still needs to be explored further.
MRI of the lung is difficult for several reasons. Major problems result from susceptibility artifacts caused by extensive air-tissue parenchymal interfaces and the low-proton density of normal parenchyma, both of which are factors that lead to low signal intensity of the normal lung. Another problem is the continuous motion of all components induced by heart pulsation and respiration, which are most prominent in the lower and anterior sections of the chest. However, proton density increases when lung tissue damage determines air space obliteration, reducing the susceptibility effects. In these cases, MRI plays a role in assessing lung parenchyma [1, 3–5] and could be useful in diagnosing pneumonia, due to the exudative accumulation of water and cells occurring in the air space.
There is some existing information on MR imaging of the lung for various diseases, including pulmonary perfusion and ventilation [1, 2, 5–9], however to our knowledge, no systematic study has been published about diagnostic MRI in patients with pulmonary tuberculosis.
The aim of our study was to compare HRCT and MRI lung examinations to identify the features of tuberculosis (TB).
Patients enrolment and characteristics
Our prospective study received institutional review board approval (INMI 3/150207) by the local ethical committee and all patients provided written informed consent.
The 50 patients (17 women and 33 men, ranging from 21-63 years of age with a median age of 47) who met our study criteria were referred to undergo HRCT and MRI imaging. The entry criteria for patients were as follows: (a) a chest X-ray with pulmonary abnormalities, (b) culture-proven pulmonary tuberculosis in culture from sputum (also induced) or bronchoalveolar lavage (c) absence of contraindication to MR examinations (ex. cardiac pacemakers, cochlear implants), (d) MRI obtained within 24 hours of the CT examination, to avoid divergent results during therapy.
All patients who did not have AIDS or additional concomitant infectious diseases were undergoing TB treatment. Altogether we performed 60 CT and MRI examinations, because 10 patients were also examined by CT and MRI at follow- up. However we analyzed the latter examinations to increment the number in our series, not to evaluate the effectiveness of therapy
Low dose HRCT was performed on all subjects using a helical four-channel MDCT scanner (Light Speed QX/i General Electric Medical System, Milwaukee, Wis). Unenhanced HRCT was obtained from the apex to the base of the lung at the end of inspiration, with 1-mm collimation, a high resolution algorithm, and 10 mm spacing. A specific mediastinum reconstruction algorithm was employed, and the images were obtained on lung and mediastinal settings.
To minimize the radiation required for obtaining diagnostic scans, the following scanning parameters were selected: tube current 70 mA, with 100 kV .
Parallel imaging MRI was performed with a 1, 5-T system (Signa Excite, General Electric Medical System, Milwaukee, Wis, USA), a maximum gradient strength of 33 mT/m, and a slew rate of 120 mT/m/s, using a six-channel body phased array coil system.
The examinations were performed with expiratory respiratory and diastolic gating. When pulsation was less vigorous, pulsation artifacts were reduced [1, 6, 8]. In agreement with the literature data , we preferred to use respiratory gating which allowed for continuous breathing instead of multiple breath hold acquisitions, also because the shifts of the lung parenchyma relative to the slice level are reduced. We performed MRI in expiration because the expiration phase is longer than the inspiration phase and signal intensity increases with deflation . Even when MRI was performed in expiratory respiration and CT at the end of inspiration, there was no significant discrepancy between the breathing positions of the images.
An axial T2-weighted Fast Recovery Fast Spin-Echo (FR FSE T2) FAT SAT was used with the following parameters: Echo Time, 90 msec; Repetition Time, 2500 msec; Echo Train Length, 14; bandwidth, 50; slice thickness, 5 mm; slice gap, 2 mm; field of view, 42 cm; matrix size, 288 × 224, reconstructed to 512.
Fat saturation sequences are very effective because the attenuated fat signal of the thoracic subcutaneous tissue reduces the ghosting artifacts of the ventral chest wall  and also increases conspicuity of fluids .
This sequence provides good image quality, and with imaging times of about 120 seconds we obtained enough slices to assess the entire lung.
The in-room time, including positioning the patient on the examination table, was approximately 15 minutes.
Both CT and MR images, all made anonymous, were directly displayed on the monitors of a picture archiving and communication system (PACS 5.1 Kodak, Rochester, NY, USA) with a window setting appropriate for lung parenchyma and mediastinum (pixel 2048 × 2560, display gradation 1021 (10-bit), maximum brightness 750cd/m2, LCD display device 54 cm). The readers were asked to assess presence, location and extension of pulmonary TB.
According to the standardized nomenclature for parenchymal findings on CT, consolidation was defined as a homogenous increase in lung parenchyma attenuation that obscures the margins of the vessels and airway walls (an air bronchogram may be present); a nodule was defined as a round lesion with a diameter of 3 cm or smaller; ground glass pattern was defined as a homogenous, hazy area of increased attenuation without obscuration of bronchovascular margins (an air bronchogram may be present); cavitation was defined as a gas-filled space, contained or not contained within a pulmonary consolidation, mass, or nodule. Tree in bud appearance was defined as a linear branching structure with more than one contiguous branching site. Furthermore, we assessed interstitial changes, in particular miliary, bronchial wall and peribronchial tissue thickening. Pleural and mediastinal lymph node involvement was also assessed.
Pleural effusion was defined as free-flowing pleural fluid producing sickle-shaped opacity (in most cases posteriorly) and loculated fluid collections as lenticular opacities in a fixed position. Pleural effusions with a volume of 15 ml or more can be detected with CT, however pleuritis sicca is not visible on CT scans. Lymph nodes were considered enlarged when they were greater than one centimeter on the short axis. Since there are no established MRI criteria to define parenchymal lung findings, we adopted the CT criteria. Regarding the pleura, MRI can detect subtle signal abnormalities that might be consistent pleuritis sicca. Concerning lymph nodes, we also assessed nodal signal intensity compared with thoracic wall muscle. Previous reports correlated histological data with MRI features in tuberculous lymphadenopathy , including signal intensity on unenhanced MR. Based on MRI findings, lymph node types could be defined according to the presence and degree of granuloma formation, caseation/liquefaction necrosis, fibrosis and calcifications. Signal intensity may differ depending on the stage of evolution: i) slight hyper-intensity may reflect lymphoid hyperplasia related to inflammation, ii) high hyper-intensity is suggestive of liquefactive necrosis, and iii) central isointensity associated with peripheral hyper-intensity may reflect caseosis.
The MRI findings to be assessed were previously established by consensus to avoid bias in individual interpretation.
All MR images were independently analyzed by two board-certified radiologists (VS, EBR, both with 10 years of experience in clinical MR imaging and 25 years of experience in chest imaging). The observers were unaware of CT results to avoid interpretation bias. Since CT is considered the gold standard technique, all CT images were considered as reference scans and were analyzed in a randomised order by the same radiologist in consensus, two months after analyzing the MR images.
Then, they directly compared MRI with CT examinations in consensus to verify the presence, distribution and characteristics of pathological features. In divergent cases, MRI and CT were re-examined to determine which imaging technique was correct. Disagreements in image scorings were resolved by consensus. MRI artifacts were graded as minimal (barely visible), moderate (clearly visible, but not interfering with evaluation) and severe (compromising evaluation). Particular attention was given to determining whether these artifacts interfered with the diagnostic value.
For CT and MR images, each parenchymal finding was scored on a scoring sheet using the following sliding scale of relative certainty: 0 = definitely negative; 1 = probably negative; 2 = indeterminate; 3 = probably positive; 4 = definitely positive. To calculate the MRI detection rate for each finding, we only considered those that were scored as 0 (definitely negative) and 4 (definitely positive).
Furthermore, for both imaging techniques, we classified each lung by zone: upper, middle, and lower, resulting in a total of six zones per patient. The upper zones were defined as areas of the lung above the level of the carina; the middle zones as areas between the level of the carina and the origin of the inferior pulmonary veins; and the lower zones as areas below the origin of the inferior pulmonary veins. Each zone had approximately the same number of sections. We scored lung zone involvement by using a four-point scale: 0 = no involvement, 1 = < 25%, 2 = 25%-50%, 3 = > 50%.
Statistical analyses were performed using the SPSS/PC+ version 11 (SPSS, Chicago, Ill). A p value lower than 0.05 indicated a statistically significant difference.
The degree of agreement between observers interpreting chest MRI was determined by using pair-wise kappa statistics as follows: very good, k value > 0.81; good, k value 0.80-061; moderate, k value 0.60-041. A separate kappa value was calculated for each sign that was reviewed.
K statistics were also calculated to analyze the agreement between MRI and CT and a detection rate for each finding; in this analysis, results were dichotomized as definitely positive or not.
The chi- square test was used to compare the proportion of images demonstrating different scores of involvement for each zone of the lungs depicted by MRI and CT.
MR artifacts were negligible in 48 cases (48/60 80%), and minimal (barely visible) in 12 cases (12/60 20%), however, these artifacts did not interfere with the diagnostic value. There were no motion artifacts or instances of image distortion due to susceptibility that resulted in poor image quality.
Findings of 60 HRCT examinations and 60 MRI examinations
Alteration consistent with caseosis
Tree in bud
(Short axis > 10 mm) 38
Alteration consistent with colliquative necrosis
Alteration consistent with caseosis
Concerning MR imaging, agreement between observers was always very good for each sign (k = 0.98-0.86).
A total of 38 lymph nodes were evaluated on unenhanced CT. Nodal involvement, assessable only as an enlargement, was seen in 16% of the cases (10/60 examinations). In the remaining 4 patients, nodal involvement (depicted by MRI as hyperintensity) was not identified on CT by the reviewers in consensus, nor at re-examination, because the nodal short axis remained < 10 mm.
Detection and percentage of pulmonary involvement in 60 HRTC and 60 MRI images
Today CT represents the gold standard for assessing lung parenchyma. MRI has some relevant clinical application, but it is not used in routine clinical management. Several recent studies clearly demonstrated that MRI can identify lung abnormalities [1, 2, 4–6, 9] with significant diagnostic advantages over CT in terms of higher contrast resolution and absence of exposure to radiation. However, CT is cheaper, more widespread, rapid to perform, and has an established role in clinical management. On the other hand, the disadvantages of MRI, such as limited spatial resolution and motion and susceptibility artifacts, have been overcome by using new techniques. In agreement with literature, our study indicates that regarding presence and distribution of pathological lung features, MRI and CT show the same results, even regarding lung tuberculosis.
Based on a one- to -one correlation between MRI and CT, the findings in both techniques regarding consolidations, nodules and cavities correlated well, and indeed obtained the same results when identifying these characteristics.
On the contrary, although MRI identified parenchymal changes, on 4 occasions it failed to diagnose "tree in bud", probably misinterpreted as interstitial changes. These false negative results for bronchogenic spread were made because of the lower MR spatial resolution. Likewise, the missed identification of interstitial changes, verified in one follow- up case, was due to very subtle involvement and lower MR spatial resolution.
Moreover small areas of "ground glass" were missed 3 times, misinterpreted as blurring.
However, because of the excellent contrast resolution, MR examinations show immediate results and are even more accurate in revealing lymph node involvement, pleural abnormalities and parenchymal caseation than unenhanced CT.
Indeed, MRI indicated nodal involvement in 14 patients and parenchymal caseation in 4 of these, features not clearly identified by the CT. However, the CT examination was unenhanced, thus could not allow for correct diagnosis. To our knowledge, no investigators have focused on the MRI features of thoracic tuberculous lympadenopathies. In our series, 89% were slight hyper-intense, 7% were isointense with peripheral hyper-intensity, and 3.5% were highly hyper-intense compared with the thoracic wall muscle. Signal intensity may differ depending on the stage of evolution, where slight hyper-intensity may indicate lymphoid hyperplasia related to inflammation, high hyper-intensity is suggestive of liquefactive necrosis, and central isointensity associated with peripheral hyper-intensity may indicate caseosis. All these findings are in line with previous reports regarding abdominal tuberculous lymphadenopathy that correlated histological data with MRI features .
Because of its excellent contrast resolution, MRI is superior to CT in assessing pleural involvement . Indeed, MRI promptly depicted pleural abnormalities with a higher percentage than CT (35% vs. 17%) with the same immediateness for subtle or loculated effusions (not seen on CT) and pleural hyper-intensity, consistent with early sicca inflammation, which was never observed on CT.
From our experience, MR was not only useful for integrating diagnostic evaluation of the lung, but the results of our study even suggest that MRI could replace CT in assessing lung tuberculosis in some subsets of patients such as children, women, during pregnancy (MR imaging should be avoided during the first trimester), follow -ups, or as an alternative to CT for patients with allergies to IV contrast material. Performing MRI in children with TB may also prove to be interesting since they may have lymph node involvement rather than lung involvement; however it should be taken into account that anaesthesia may be required.
We believe that MRI is comparable to CT for identifying morphological pulmonary changes, and that MRI is clearly superior to CT regarding tissue characterization. Furthermore, on the basis of lesion signal intensity, MRI could differentiate the exudative stage of lung TB from the relatively acellular fibrotic phase because of the relatively "short T2" in fibrotic tissues .
The shortcomings of our study are the limited number of patients and the absence of miliary and calcified nodules found in the enrolled patients, thus it could not be proved that these lesions can be identified by MRI. The lack of histopathological correlation or microbiological tests of the adenopathies is another important limitation of the study, and MRI in the phase of expiration may show non-pathological processes such as small laminar atelectasis. Moreover, further studies are needed to determine whether the use of FR FSE T2 sequences without fat sat might improve visualization of the parenchyma.
The authors are grateful to all the patients, nurses and technicians (in particular M.R.Longo, D.Di Bartolomeo, M.Bianchetti, M.Morea, V.Possanzini) who took part in the study. The authors thank Ms Andrea Baker for editing the manuscript.
- Leutner CC, Gieseke J, Lutterbey G, Kuhl CK, et al: MR Imaging of Pneumonia in Immunocompromised Patients: Comparison with Helical CT. AJR. 2000, 175: 391-397.View ArticlePubMedGoogle Scholar
- Eibel R, Herzog P, Dietrich O, Rieger CT, et al: Pulmonary Abnormalities in Immunocompromised Patients: Comparative Detection with Parallel Acquisition MR Imaging and Thin-Section Helical CT. Radiology. 2006, 241: 880-891. 10.1148/radiol.2413042056.View ArticlePubMedGoogle Scholar
- Herold CJ, Kuhlmann JE, Zerhouni EA: Pulmonary Atelectasis: Signal Patterns with MR Imaging. Radiology. 1991, 178: 715-720.View ArticlePubMedGoogle Scholar
- Eibel R, Herzog P, Dietrich O, Rieger CT, Ostermann H, Reiser M, Schoenberg S: Magnetic Resonance Imaging in the Evaluation of Pneumonia. Radiology. 2006, 46: 272-274.Google Scholar
- McFadden RG, Carr TJ, Mackie IDF: Thoracic Magnetic Resonance Imaging in the Evaluation of HIV-1/AIDS Pneumonitis. Chest. 1992, 101: 371-374. 10.1378/chest.101.2.371.View ArticlePubMedGoogle Scholar
- Lutterbey G, Gieseke J, von Falkenhausen M, Morakkabati N, Schild H: Lung MRI at 3.0T: A Comparison of Helical CT and High-Field MRI in the Detection of Diffuse Lung Disease. Eur Radiol. 2005, 15: 324-328. 10.1007/s00330-004-2548-1.View ArticlePubMedGoogle Scholar
- Eichinger M, Heussel CP, Kauczor HU, Tiddens H, Puderbach M: Computed Tomography and Magnetic Resonance Imaging in Cystic Fibrosis Lung Disease. J Magn Reson Imaging. 2010, 32 (6): 1370-8. 10.1002/jmri.22374.View ArticlePubMedGoogle Scholar
- Ley-Zaporozhan J, Puderbach M, Kauczor HU: MR for the Evaluation of Obstructive Pulmonary Disease. Magn Reson Imaging Clin N Am. 2008, 16 (2): 291-308. 10.1016/j.mric.2008.02.014.View ArticlePubMedGoogle Scholar
- Kauczor HU, Ley-Zaporozhan J, Ley S: Imaging of Pulmonary Pathologies. Focus on Magnetic Resonance Imaging. Proc AM Thorac Soc. 2009, 6: 458-463. 10.1513/pats.200901-002AW.View ArticlePubMedGoogle Scholar
- Busi Rizzi E, Schininà V, Gentile FP, Bibbolino C: Reduced Computed Tomography Radiation Dose in HIV-related Pneumonia: Effect on Diagnostic Image Quality. Clin Imaging. 2007, 31 (3): 178-184. 10.1016/j.clinimag.2006.09.026.View ArticleGoogle Scholar
- Puderbach M, Hintze C, Ley S, Eichinger M, Kauczor HU, Biedere J: MR Imaging of the Chest: A Practical Approach at 1.5 T. E J Radiol. 2007, 64: 345-355. 10.1016/j.ejrad.2007.08.009.View ArticleGoogle Scholar
- Lutterbey G, Grohè C, Gieseke J, von Falkenhausen M, et al: Initial Experience with Lung-MRI at 3.0T: A Comparison with CT and Clinical Data in the Evaluation of Interstitial Lung Disease Activity. E J Radiol. 2007, 61: 256-261. 10.1016/j.ejrad.2006.09.005.View ArticleGoogle Scholar
- De Backer AI, Mortelè KJ, Van Den Heuvel E, Vanschoubroeck IJ, Kockx MM, Van de Vyvere M: Tuberculous Adenitis: Comparison of CT and MRI Findings with Histopathological Features. Eur Radiol. 2007, 17: 1111-1117. 10.1007/s00330-006-0412-1.View ArticlePubMedGoogle Scholar
- Knisely BL, Broderick LS, Kuhlman JE: MR Imaging of the Pleura and Chest Wall. Magn Reson Imaging clin N Am. 2000, 8: 125-41.PubMedGoogle Scholar
- Berthezene Y, Vexler V, Kuwatsuru R, Rosenau W, Muhler A, Clement O, et al: Differentiation of Alveolitis and Pulmonary Fibrosis with a Macromolecular MR Imaging Contrast Agent. Radiology. 1992, 185: 97-103.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/11/243/prepub
This article is published under license to BioMed Central Ltd. 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.