3 Tesla proton MRI for the diagnosis of pneumonia/lung infiltrates in neutropenic patients with acute myeloid leukemia: Initial results in comparison to HRCT☆
Introduction
The incidence of systemic fungal and other atypical pulmonary infections is increasing in severely immunocompromised neutropenic patients suffering from acute leukemia. Among these, invasive fungal infections such as pulmonary aspergillosis are associated with particularly high mortality [1]. Thus, early diagnosis and subsequent initiation of appropriate treatment is essential in order to improve patient outcomes. However, serological and microbiological markers are known to be of only limited sensitivity in the diagnosis of these conditions and exhibit poor specificity [1]. Thus, the mortality associated with such infections remains high. In immunocompromised patients, systemic fungal infections manifest primarily as fungal pneumonia. High-resolution computed tomography (HRCT) [2] plays a pivotal role in the diagnostic work-up due to its proven high sensitivity (∼90%) [3]. However, CT findings are often equivocal, diminishing diagnostic confidence and necessitating repetitive imaging at the expense of high cumulative radiation doses in patients who are frequently young.
Given the improved soft tissue contrast and the lack of ionizing radiation, MRI is considered a promising diagnostic alternative to HRCT [4], [5], [6], [7], [8]. Specific anatomical considerations in the lung, such as the multiple air-soft tissue interfaces, lead to greater T2* related susceptibility effects and thus present challenges to pulmonary MRI, particularly at 3 Tesla. Nevertheless, imaging at higher field-strengths may potentially improve the characterization of pulmonary infections in neutropenic patients due to high signal-to-noise and contrast-to-noise ratios at simultaneously high spatial resolutions [1], [9], [10], [11], [12], [13], [14]. These factors may prove particularly beneficial in the detection of hemorrhage which is seen characteristically in angioinvasive aspergillosis – a common infectious entity in neutropenic patients.
Thus the aim of this study was to evaluate the role of MR at 3 Tesla, in comparison to HRCT, for the assessment of pulmonary infections, especially invasive pulmonary aspergillosis in neutropenic patients with acute myeloid leukemia (AML).
Section snippets
Patient population
From 2009–2011, a total of 19 neutropenic, febrile acute myeloid leukemia (AML) patients (5 women, 14 men; mean age 61 years ± 14.2; range 23–77 years) were included in this prospective study. Institutional review board (IRB) approval was obtained, and the study followed the principles of the Declaration of Helsinki and its subsequent amendments. All patients underwent chest HRCT according to diagnostic guidelines [15], followed by MRI within 24 h. Criteria for inclusion were host factors
Results
All HRCT and MRI examinations were successfully completed without any adverse events and no study was excluded from data analysis due to insufficient image quality. A total of 95 pulmonary lobes were evaluated in terms of the presence, localization, and characteristics of abnormalities on both MRI and CT. In 51 lobes (19 of 19 patients) CT and MRI abnormalities were determined to be concordant by both readers in terms of the presence, localization, and type of abnormality (true positives). In
Discussion
The results of the present study demonstrate the promise of 3 T MRI as an alternative imaging modality to HRCT for the evaluation of acute pulmonary infections in immunocompromised patients. The comparison between HRCT and MRI in this specific patient cohort finds an overall diagnostic accuracy for MRI of 88%. Both consolidations and nodular opacities were detected accurately by MRI with good concordance to HRCT. Overall lesion localization with MRI was also comparable to that achieved by HRCT.
Conflict of interest
Ulrike Attenberger: Consultant: Research Consultant, Bayer Healthcare. Other: Institutional Research Agreement, Siemens AG.
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This work was supported by a grant (#R 08/12v), provided by the José Carreras Leukämie-Stiftung.