Abstract
BACKGROUND AND PURPOSE: It is known that intracranial mass lesions are relatively isotropic on diffusion-weighted imaging. The purpose of this study is to report an unusually high fractional anisotropy (FA) and mean diffusivity (Dav) in the cavity of the brain abscess compared with other cystic lesions.
METHODS: We performed diffusion tensor imaging (DTI) in 12 patients with cystic intracranial lesions (pyogenic abscess, n = 5; cysticercus cysts, n = 2; and low-grade astrocytoma, n = 5). Mean FA, Dav from the lesion core, perifocal edema, and corresponding contralateral normal-appearing regions were measured and compared for relative changes in these parameters. In the abscess cases, we placed regions of interest on areas with FA >0.2 and FA <0.2 to get FA and Dav values.
RESULTS: There were two patterns of FA values in the abscess cavity in all five patients. Part of the abscess showed mean FA = 0.440 ± 0.135, with Dav = (0.993 ± 0.185) × 10−3 mm2/s, whereas other parts had FA = 0.131 ± 0.039 with Dav = (0.824 ± 0.183) × 10−3 mm2/s. The cystic tumors and neurocysticercosis showed very high Dav = (2.806 ± 0.25, 2.654 ± 0.35)× 10−3 mm2/s, with low FA = (0.108 ± 0.037, 0.08 ± 0.01), respectively.
CONCLUSION: Brain abscess cavity shows regions of increased FA values with restricted mean diffusivity compared with other cystic intracranial lesions. This information may prevent misinterpretation of the DTI information as white matter fiber bundle abnormalities associated with mass lesions.
Diffusion is anisotropic in white matter fiber tracts, as axonal membranes and myelin sheaths present barriers to the motion of water molecules, in directions not parallel to their own orientation (1). The direction of maximal diffusivity has been shown to coincide with the white matter tract information. This information is contained in the diffusion tensor, a mathematical construct of diffusion in 3D space (1, 2). Currently, information about fiber tracts obtained from diffusion tensor imaging (DTI) is being used by neurosurgeons in the planning of tumor resection (2).
A brain abscess is characteristically defined as a focal suppurative process within the brain parenchyma (3). It forms important differential diagnosis with other tumor and nontumor ring-enhancing brain lesions (3). MR imaging techniques such as proton MR spectroscopy and diffusion-weighted (DW) imaging have been used in the differentiation of abscesses from nonabscess lesions with considerable success (4–6). Although most abscesses show restricted diffusion, there are reports showing high diffusivity in the treated abscesses and restricted diffusion in cystic metastases (4, 7, 8). It is proposed that combining DW imaging with in vivo proton MR spectroscopy may help in better characterization of these lesions (6).
In this work, we report remarkably high fractional anisotropy (FA) from the cavity of brain abscess in five patients with restricted mean diffusivity in comparison to nonabscess cases. An attempt is made to explain this unusual observation, which, to the best of our knowledge, is described here for the first time in the literature.
Subjects and Methods
We performed MR imaging, including DTI, on 12 consecutive subjects with various intracranial mass lesions. There were seven male and five female subjects ranging in age from 4 to 55 years. Five patients had brain abscess, five had low-grade astrocytoma, and two had neurocysticercosis (NCC). In the two patients with NCC, there were a total of five cysts of >2 cm in diameter. The diagnosis in the abscess and tumor patients was based on aspiration and culture of the pus and histopathologic reports in cystic neoplasm, respectively. The source of primary infection was otitis media (n = 2), orbital infection (n = 1), and tooth infection (n = 2). The pus was evaluated for the number of viable leukocytes and microbial culture. The final diagnosis in patients with NCC was based on the demonstration of scolex on conventional imaging and CSF serology (enzyme-linked immunosorbent assay) positive for the parasitic antigen (9). Repeat imaging, including DTI, was also performed in three patients with abscess to look for the changes in FA following aspiration of the pus. We have also obtained DTI data from 10 healthy age- and sex-matched control subjects for the purpose of comparison with these subjects.
MR Imaging Protocol
Whole-brain conventional MR imaging and DTI were acquired on a 1.5-T MR imaging scanner (General Electric Medical System, Milwaukee, WI) using a standard quadrature birdcage receive and transmit radio-frequency head coil. The conventional MR imaging protocol included T2-weighted fast spin-echo (SE) images with repetition time TR/TE/NEX) = 6000/200/16/2 and SE images with TR/TE/NEX = 1000/14/1. Both T1- and T2-weighted images were acquired from axial sections of 5-mm section thickness with 0.5-mm intersection gap and 240-mm FOV. Postcontrast T1-weighted magnetization transfer (MT) MR imaging was done after injecting gadolinium diethylenetriaminepenta-acetic acid in the dose of 0.1 mmol/kg body weight (Schering, Berlin, Germany), using the same parameters as T1 except for the off-resonance pulse (1.2 kHz) with pulse duration of 16 milliseconds and 670° flip angle to improve the sensitivity of the enhancement.
DTI data were acquired using a single-shot echo-planar dual SE sequence with ramp sampling (10, 11). The dual SE sequence reduces image distortions in the diffusion-weighted images by compensating for the effect of eddy currents as shown elsewhere (12). The sequence used spectral-selective pulses for fat suppression. The diffusion-weighted sequence incorporated symmetric trapezoidal gradient pulses with pulse duration (δ ∼ 25) and separation (Δ ∼ 28 ms). The diffusion weighting b-factor was set to 1,000 s/mm−2, TR ∼ 8 seconds, and TE ∼ 100 ms. A total of 20–34 axial sections were acquired with a section thickness of 3 mm, no gap, FOV = 240 mm x 240 mm, and an image matrix of 256 × 256 (following zero-filling). The diffusion tensor encoding used was the balanced (13), rotationally invariant (14, 15) icosahderal scheme with 21 uniformly distributed directions over the unit hemisphere. To enhance the signal intensity-to-noise ratio (SNR) and reduce phase fluctuations, the magnitude constructed images were repeated (NEX = 4) and temporally averaged by the scanner software (10). The SNR0 in the (b ∼ 0) image was about 50 (parenchyma), which reduces the SNR-related biases in the DTI estimated metrics (15, 16). Data from a spherical water phantom were also acquired at 19°C by using the same DTI scheme for the purpose of b-factor calibration.
DT-MR Imaging Data Analysis
The magnitude-averaged data were transferred via file transfer protocol to a workstation for further analysis. In general, the DTI data analysis involves three major steps: preprocessing, processing, and postprocessing.
Data Preprocessing
The collected raw images were cropped and stripped using a semiautomated procedure to remove the scalp for isolating the brain. The DW imaging data were spatially filtered with a 3 × 3 median window. The data were then distortion-corrected for shear, scale, rotation, and translation by using the DT-MR imaging toolbox, which calls the 2D perspective models in the automated image and registration package (17, 18).
Data Processing
The distortion-corrected data were then interpolated to attain isotropic voxels and decoded to obtain the tensor field for each voxel. The tensor-filed data were then diagonalized using the analytical diagonalization method (19) to obtain the eigenvalues (λ1, λ2, and λ3) and the three orthonormal eigevectors (e1, e2, and e3). The tensor field data and eigenvalues were then used to compute the DTI metrics such as the mean diffusivity (Dav; equation 1) and fractional anisotropy (20) (FA; equation 2) for each voxel.
1) |
Data Postprocessing and Quantification
To facilitate region-of-interest placement for quantitative analysis, the DTI-derived maps were displayed and overlaid on images with different contrasts in the three orthogonal planes for a visual inspection. FA regional values were obtained by placing the regions of interest on the abscess cavity and other cystic lesions on all sections that contained the lesions. The region-of-interest placement on the lesions was based on the FA maps overlayed on the Dav with a cut-off value of 0.20 so that voxels could be separated between the ones with FA values >0.20 and <0.20 for all the cystic lesions. This threshold was chosen because white matter was found to have this as minimal of 0.2 FA value in hundreds of brain images that we had analyzed. In addition, the same regions of interest were placed on the perifocal edema and the corresponding contralateral normal-appearing parenchyma as depicted by T2-weighted images. Size of the regions of interest was guided by the lesion size, and it was always more than 3 × 3 pixels in all the cases and typically 8 × 8 pixels, with shape varying from elliptical to rectangular. Data processing and analysis were performed using the analysis and design DTI-toolbox implemented under interactive data language (IDL) (Research Systems, Boulder, CO). FA and Dav from the whole brain from three healthy subjects were also quantified for the purpose of comparison.
Results
Water Phantom Data
For the purpose of quality control and b-factor calibration of the scanner gradient system, quantitative FA and diffusivities data were obtained from 25,000 voxels at the center of the water phantom gave λ1 = (2.05 ± 0.08) × 10−3 mm2/s, λ2 = (1.99 ± 0.07) × 10−3 mm2/s, λ3 = (1.90 ± 0.06) × 10−3 mm2/s, Dav = (1.98 ± 0.06) × 10−3 mm2/s, and FA = 0.04 ± 0.02. Our water phantom calibration results are consistent with published literature at comparable room temperature (21).
Clinical Data
The abscesses were located in the right caudate nucleus (n = 2), right temporal lobe (n = 1), right temporoparietal region (n = 1), and right frontal region (n = 1). These appeared hyperintense on T2-weighted images with peripheral hypointense rim, and iso- to hypointense on T1-weighted images. Postcontrast study showed rim enhancement. In one patient, the abscess ruptured into the right lateral ventricle with layering on T2, T1, and DW images and showed low Dav and high FA values in the layer (Fig 1). The culture from the pus grew S. aureus (n = 2), anaerobic streptococci (n = 2), and Pseudomonas aeruginosa (n = 1). The viable leukocyte count varied from 7,000 to 16,000 in all the abscess cases. The tumors were located in the cerebellum (n = 2), brain stem (n = 1), right parietal (n = 1), and left frontotemporal region (n = 1). These appeared hyperintense on T2 and hypointense on T1 and showed rim enhancement on postcontrast study. There was no viable cell visible on microscopy in the fluid obtained from the tumor cavity.
The axonal fibers around the cystic lesions showed displacement with marked decrease in FA values in the regions of edema when present focally. The changes in FA at different locations of the abscess, cystic tumors, NCC, and corresponding contralateral normal-appearing white matter and from the normal healthy individuals are plotted against Dav (Fig 2). Part of the abscess with FA >0.2 and <0.2 showed mean FA = 0.440 ± 0.135 with Dav = (0.993 ± 0.185) × 10−3 mm2/s, and FA = 0.131 ± 0.039 with Dav = (0.8237 ± 0.183) × 10−3 mm2/s, respectively (Figs 1–3). The cystic tumors (Fig 4) and NCC (Fig 5) showed very high Dav = (2.806 ± 0.25) × 10−3 mm2/s, (2.654 ± 0.35) × 10−3 mm2/s with low FA values ∼ (0.108 ± 0.037 and 0.08 ± 0.01), respectively. The mean FA and Dav values from the perifocal edema normal-appearing corresponding contralateral parenchyma were 0.0751 ± 0.021, 0.208 ± 0.07, and (1.708 ± 0.27, 1.096 ± 0.13) × 10−3 mm2/s, respectively. The Dav values were toward the higher side compared with the normal healthy subjects and the normal values reported in the literature (10). This is probably due to voxel contamination with CSF and the effect of pressure on the contralateral lobe by the pathology causing the increased water content in these regions. In three patients with brain abscess, a repeat study following surgical intervention showed a marked decrease in the residual cavity with no restriction of diffusion (Fig 3).
Discussion
The effect of cerebral neoplasm on the white matter tracts has been described using DTI as compressive, discontinued in the region of edema or tumor, or disrupted due to tumor infiltration (2, 22–24). This information was found to be useful for the purpose of tumor resection. We also observed displacement of the axons surrounding the lesions irrespective of the nature of the lesion along with low FA values in the region of the perifocal edema. In addition, in this study we observed markedly increased FA in the cavity of the abscess with different orientations that was not observed in the cavity of the cystic astrocytomas and neurocysticercosis (Figs 1–5).
The MR features of a brain abscess vary with the lesion stage. During the initial cerebritis stage, an ill-defined subcortical hyperintense zone on T2-weighted images is associated with poorly delineated enhancing areas within the iso- to mildly hypointense edematous region on enhanced T1-weighted images. During the early and late capsule stages, the collagenous abscess capsule is visible on precontrast study as a comparatively thin-walled, well-delineated iso- to slightly hyperintense rim that becomes hypointense on T2-weighted sequences (3). These abscesses usually show restricted diffusion on DW imaging with low mean diffusivity (3, 5, 6). The purulent material obtained from the abscess cavity at the time of surgery shows inflammatory cells, necrotic cellular debris, proteins, and amino acids as well as low molecular weight metabolites (3, 25). In the present study, in addition to low diffusivity, we observed high FA in some part of the abscess cavity with orientation on the principal eigenvector maps in all of these cases. The FA values are as high as the normal white matter with orientation apparently suggesting an oriented structure within the cavity. Histologically, there was no structure other than the inflammatory cells, necrotic debris, proteins, and amino acids (3, 25). The high FA with low mean diffusivity has been described by several authors in cerebral ischemia and infarction. The previously reported FA values, however, were not as elevated as those observed in the current study (26–29). Recently, it has been shown that FA has a significant inverse correlation with T2 signal intensity in hyperacute stroke and there was no relation with Dav measures (29). It was proposed that the initial decrease in extracellular water resulted in high FA and low Dav (29). Increased FA has also been found in the first 24 hours after trauma with increased T2 and no change in Dav (30). This has been explained by an increase in the largest (λ1) eigenvalue coupled with a proportionately smaller decrease in the smallest (λ3) eigenvalue (30). The present clinical situation, however, is not similar to hyperacute stroke or acute traumatic brain injury and therefore cannot be explained on this basis. We propose that the inflammatory cells in the abscess cavity become oriented and organized, resulting in high diffusion anisotropy. The current observation, however, challenges the traditional view that brain anisotropy usually represents myelination and axonal packing (1, 2, 10, 11, 23, 24) and calls for some caution in the interpretation of DTI data.
A number of studies have reported DTI results in brain tumors. The tumors have been shown to displace white matter tracts due to mass effect. In all published studies, there is an isotropic diffusion at the center of the cystic tumor cavity (3, 22, 24). We have observed 0–5 intact cells/mm3 in the fluid obtained from 45 cystic brain neoplasms and three cysticercus cysts (authors’ unpublished data). On the other hand, a large number of intact inflammatory cells were seen in these patients with brain abscess. One possibility could be that these cells are tightly packed, thus reducing the extracellular space and therefore are responsible for a large anisotropy in the abscess cavity; however, this explanation is less likely. This is because we observed regions in the abscess cavity with high FA and restricted diffusion and another with low FA and restricted diffusion (Figs 1–3). Larger variation in FA values without a great difference in Dav of the abscess cavity suggests that FA does not have a strong relationship with Dav in the abscess model (Fig 2).
The host response to the microorganisms consists of three pathologic mechanisms: tissue inflammation, granuloma, and abscess formation (31). The presence of bacteria challenges the expression of leukocytes that are activated by its presence. This results in a release of large amounts of chemotactic peptides and an up-regulation of intracellular adhesion molecules (ICAM-1) that are recruited to the cell surface to mediate their aggregation via lymphocyte function-associated molecule 1 (LFA-1) (31–33). A large cellular aggregation has been shown by incubating the bacteria with the leukocytes after 5 hours that firm up after 24 hours (32). The capsular stage of the brain abscess occurs from the 10th day onward and is associated with the formation of a well-vascularized wall that sequesters the lesion. The cavity of the lesion contains inflammatory cells, bacteria, and debris (3). In the present study, viable leukocytes were found in the cavity and have grown microorganisms responsible for the abscess formation on pus culture. We postulate that the regions with high FA values in the cavity of the abscess contain aggregated (clumped) leukocytes due to the presence of adhesive molecules that are known to be up-regulated in the presence of bacteria. Low FA in some regions of the abscess cavity probably reflects areas devoid of leukocytes with adhesive properties due to the relative lack of up-regulation of the adhesive molecules on the surface of the remaining leukocytes. This hypothesis, however, needs confirmation by performing further studies to demonstrate the adhesive molecules on the surface of the leukocytes with cell clumping.
Conclusion
The present study demonstrates that brain abscess cavity shows regions of increased FA values with restricted mean diffusivity compared with other cystic intracranial lesions. With an increasing use of DTI in surgical planning of brain-tumor resection, one may become more careful in interpreting these changes as oriented axonal fibers.
Footnotes
Supported by a grant from Indian Council of Medical Research, New Delhi, India.
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