Abstract
BACKGROUND AND PURPOSE: Susac syndrome is a rare disorder consisting of encephalopathy, hearing loss, and retinal arteriolar occlusions. The purpose of this study was to evaluate the evolution of lesions in this disease by using serial MR imaging with diffusion-weighted imaging (DWI) and apparent diffusion coefficients (ADCs). Abnormalities in the nonlesional white matter (NLWM) were also analyzed.
METHODS: Serial MR and DWI findings in two patients with Susac syndrome were reviewed retrospectively. ADCs of the lesions and the NLWM were compared with values of the corresponding anatomical regions in 16 control subjects.
RESULTS: T2-weighted images, DWIs, and fluid-attenuated inversion-recovery (FLAIR) images demonstrated diffuse small hyperintense lesions predominantly involving the corpus callosum, white matter, cerebral cortex, and deep gray structures. During the whole course in the two patients, 437, 295, and 113 lesions were depicted on FLAIR images, T2-weighted images, and DWIs, respectively. With the aggravation and mitigation of the clinical symptoms, the size and number of the lesions changed over time. Of 65 lesions with measured ADCs, six had restricted ADCs (5.29–6.91 × 10−4 mm2/s), and 29 had elevated ADCs (8.02–13.5 × 10−4 mm2/s). With disease progression, ADCs in the NLWM changed from normal to elevated; this corresponded to the diffuse signal-intensity change seen in the white matter.
CONCLUSION: FLAIR imaging is the most sensitive sequence for detecting lesions of Susac syndrome. DWI is useful in demonstrating the heterogeneous nature of lesions, depicting occult abnormalities in the white matter, elucidating underlying pathologic processes, and conducting patient follow-up.
Susac syndrome is a rare disease that Susac et al first described in 1979 (1). It is characterized by acute or subacute encephalopathy, sensorineural hearing loss, and occlusions of the retinal artery branch caused by a microangiopathy involving the brain, cochlea, and retina. The pathogenesis of this syndrome is unknown. The disease may have a self-limited course, but patients usually have residual cognitive, visual, and/or hearing disability (2, 3).
Brain imaging is part of the routine diagnostic evaluation for suspected Susac syndrome, given the involvement of the CNS. MR imaging is expected to provide an exquisite evaluation of the lesions of Susac syndrome because microinfarctions are believed to be the basic histologic feature of the lesions (2–5). In addition to T2-weighted and fluid-attenuated inversion-recovery (FLAIR) imaging, diffusion-weighted imaging (DWI) and apparent diffusion coefficients (ADCs) have been proved to be sensitive to the histologic and physiologic changes associated with brain infarction and are useful in assessing these changes over time (6–9). We therefore hypothesized that DWI and ADCs enable a unique analysis of the lesions in Susac syndrome, which pathologically consist of changes consistent with areas of microinfarction.
The purpose of this study was to describe the evolution of multiple lesions in patients with Susac syndrome on serial MR images, with DWIs, ADC values, T2-weighted images, and FLAIR images. Abnormalities in the nonlesional white matter (NLWM) were also analyzed. A number of case reports on Susac syndrome have described the MR appearance of the brain (2–5, 10–19); however, only a few include the serial MR appearance (3, 4). To our knowledge, DWI and ADCs in patients with Susac syndrome have not been previously described.
Methods
We retrospectively reviewed serial MR findings, including those of DWIs, in two patients with Susac syndrome. Each was imaged four times within 8 or 11 months. ADC values were calculated for 65 noncortical lesions (36 in patient 1, 29 in patient 2) and 64 regions in NLWM. These values were quantitatively compared with ADC values from corresponding anatomic regions in 16 control subjects. An additional 45 cortical lesions were not included in the statistical analysis because of possible partial voluming of CSF into the ADC measurements. The institutional review board at our hospital approved this study.
Patient Histories and Clinical Presentations
Patient 1.—
A 21-year-old African American woman presented with a 2-week history of encephalopathy. Fluorescein angiography showed an occlusion of the right retinal artery branch. She was treated with steroid therapy and, within 2 weeks, her symptoms moderately improved. The patient was readmitted with recurrent encephalopathy 8 weeks after the initial onset. Fluorescein angiography showed two new occlusions of the left retinal artery branch, and audiography demonstrated high-frequency hearing loss on the left side. Her condition substantially improved after 2 months of steroid therapy. Over the next 8 months, the patient appeared to have improved, as she was discharged with steroid treatment. An ophthalmologic examination was performed at 9 months from initial onset, and her condition was stable with no new occlusion of the retinal artery branch. After that, she failed to keep her clinic appointment.
Patient 2.—
A 49-year-old woman presented with acute onset of partial vision loss in the right eye and a 2-week history of headaches. Fluorescein angiography showed an occlusion of the right retinal artery branch and a visible embolus. She was treated with aspirin and discharged home in stable condition about 1 month later. The patient was readmitted with encephalopathy at 6 weeks after her initial presentation. Ophthalmologic examination showed a new occlusion of the retinal artery branch in her left eye. She was treated with immunosuppressive therapy. About 1 month later, the encephalopathy was notably improved. However, it relapsed 4 months later, at which time ophthalmoscopy showed new occlusions of the retinal artery branch in her left eye. An audiogram demonstrated partial hearing loss in the right ear. After treatment with more-aggressive steroid therapy, she had good clinical improvement. At 11 months from initial onset, the patient presented with worsening vision and encephalopathy. She received steroid therapy again and improved somewhat. In the following year, her symptoms recurred repeatedly and mitigated after treatment. After about 2 years from initial onset, the patient had major improvement with no vision or hearing impairment.
Diagnosis of Susac Syndrome.—
In both the patients, extensive hematologic studies, including autoimmune panels, were unremarkable. Four-vessel cerebral angiograms were normal. In each case, Susac syndrome was diagnosed on the basis of coexistent encephalopathy, retinal artery occlusions, and hearing dysfunction. The clinical course, symptoms, auditory findings, retinal findings, and treatments in the two patients are summarized in Table 1.
Clinical histories and presentations in patients with Susac syndrome
Image Acquisition
The initial (2 weeks from onset) and third (10 weeks from onset) MR examinations in patient 1 were performed with a 1.5-T superconducting magnet (Magnetom Vision; Siemens, Erlangen, Germany). Conventional MR imaging included an axial T1-weighted spin-echo (SE) sequence (TR/TE, 700/14 or 600/14; matrix, 256 × 512 or 192 × 512; field of view, 24 × 24), an axial T2-weighted fast SE sequence (TR/TE, 3986/99; matrix, 264 × 1024 or 308 × 1024; field of view, 24 × 24), and a FLAIR sequence (TR/TE/TI, 9000/105/2700; matrix, 182 × 256; field of view, 24 × 24). Before the administration of contrast agent, axial DWIs were acquired by using a single-shot echo-planar imaging sequence (TR/TE, 5400/103; matrix, 96 × 200; field of view, 25 × 25). A reference T2-weighted intensity image (b = 0.0 s/mm2) and three orthogonally oriented DWIs (b = 1000 s/mm2) were obtained at each transverse section.
The second (8 weeks from onset) and fourth (8 months from onset) MR examinations in patient 1 and the four examinations (2 and 8 weeks, 4 and 11 months) in patient 2 were performed with a 1.5-T superconducting magnet (Signa; GE Medical Systems, Milwaukee, WI). Conventional MR imaging consisted of an axial T1-weighted SE sequence (583/20; matrix, 192 × 256; field of view, 24 × 24), an axial T2-weighted fast SE sequence (3000/100; matrix, 256 × 256; field of view, 24 × 24), and a FLAIR sequence (9002/165/2700; matrix, 182 × 256; field of view, 24 × 24). Before the administration of contrast agent, axial DWIs were acquired by using a single-shot echo-planar imaging sequence with a TR/TE of 5000/94.7, a matrix of 128 × 128, and a field of view of 32 × 32. A reference T2-weighted intensity image (b = 0.0 s/mm2) and a diffusion trace image (b = 1000 s/mm2) were obtained at each transverse section. The latter was an image with minimized diffusion anisotropy and created from the average of three orthogonal diffusion directions.
All images were acquired with a section thickness of 5 mm and an intersection gap of 2 mm. Contrast-enhanced axial and coronal T1-weighted images, obtained after injection of gadopentetate dimeglumine (0.1 mmol/kg), were obtained at the initial and second examinations in patient 1 and at every examination in patient 2.
Sixteen control subjects without neurologic symptoms were also imaged with identical protocols (10 with the GE Medical Systems unit and six with the Siemens unit).
Image Analyses
Lesion location, number, size, signal intensity, and enhancement were evaluated. How these findings changed over time were studied. A lesion was defined as a focus of hyperintensity, as depicted on T2-weighted images, FLAIR images, and/or DWIs. Some small hyperintensities, which appeared in a cluster pattern (especially in the corpus callosum) were counted as multiple lesions, though some might have been different parts of a single lesion. Because of the lack of clear separation, it was sometimes difficult to determine which were individual lesions or parts of a single lesion.
DWIs were reviewed on a workstation (ADW 4.0; GE Medical Systems). ADC values were calculated as follows: ADC = −[ln(S/S0)]/b, where S is the signal intensity of the region of interest obtained through three orthogonally oriented DWIs or diffusion trace images, S0 is the signal intensity of the region of interest acquired through reference T2-weighted intensity images, and b is the gradient b factor with value of 1000 s/mm2.
We recorded ADC values from the lesions detected on DWIs in both patients. Changes in the ADC values were evaluated during follow-up. However, because most of the lesions were small, and the location of the axial sections was not the same on every examination, the size and shape of the lesions appeared different during follow-up, and ADC changes for specific lesions could not be assessed. Several small lesions of the corpus callosum were near the CSF of the ventricles, and their ADC values could not be accurately measured. Differences of ADC values between pathologic lesions and corresponding anatomic regions in control subjects were compared by calculating a z-score. A significant difference was accepted if the z-score was above 2 or below -2.
ADC values of NLWM were also measured and compared with the mean values of white matter from the control subjects. NLWM was defined as white matter without visible focal abnormalities on T2-weighted images, FLAIR images, or DWIs. The statistical significance of differences was determined by using the paired t test. Changes in signal intensity in the NLWM were also evaluated.
Results
Lesions at MR Imaging
Patient 1.—
The initial MR examination, performed 2 weeks after onset of symptoms, demonstrated extensive small T2 hyperintensities in the cerebral white matter, corpus callosum, bilateral basal ganglia, bilateral middle cerebellar peduncles, and bilateral cerebellar hemispheres. The lesions were predominantly supratentorial. Particularly distinct was a cluster of lesions in the corpus callosum. On FLAIR images, the lesions were also hyperintense, and most were more conspicuous than on other images. Lesions in the cerebral cortex were not well seen on T2-weighted images and better depicted on FLAIR images (Fig 1A–D). The total number of lesions was at least 57 on T2-weighted images and 68 on FLAIR images. The largest diameter of most lesions varied from several millimeters to about 10 mm. The lesions on T1-weighted images, especially those in the corpus callosum, were seen as small hypointensities. On contrast-enhanced T1-weighted images, multiple, tiny foci of enhancement were found in the cerebellar hemispheres and basal ganglia bilaterally. Diffuse leptomeningeal enhancement was also noted (Fig 1E). DWIs depicted at least 19 hyperintense lesions in the cerebral white matter, basal ganglia, cerebellum, and corpus callosum (Fig 1F). The second MR examination, at the time of relapse, was performed 8 weeks after the initial onset of symptoms. T2 and FLAIR hyperintensities previously seen in the corpus callosum and cerebellar hemispheres were decreased in size and number. Some lesions could not be detected. There was no evident enhancement of these small lesions, though leptomeningeal enhancement persisted. Numerous new hyperintense punctate lesions were found in the cerebral cortex, mainly on FLAIR images and DWIs (Fig 2). In addition, several questionable, tiny T2 and FLAIR hyperintensities appeared in the posterior limbs of the internal capsules. Because of the normal variation of cortical contrast on brain DWIs, separating subtle lesions in the cortex from this normal variation is difficult. Therefore, judgments about the presence of subtle cortical lesions were subjective.
Patient 1. Initial MR examination at 2 weeks from the onset of symptoms.
A and B, Axial T2-weighted images show multiple hyperintense lesions involving the corpus callosum and cerebral white matter.
C and D, Axial FLAIR images at almost the same levels as in A and B show hyperintense lesions not only in the corpus callosum and cerebral white matter but also in the cerebral cortex (arrows).
E, Contrast-enhanced axial T1-weighted image shows diffuse leptomeningeal enhancement.
F, Axial DWI shows several hyperintense lesions in the cerebral white matter (arrows), with a cluster of lesions in the corpus callosum.
Patient 1. Second MR examination shortly after relapse of the symptoms (8 weeks from initial onset).
A and B, Axial FLAIR images show that the lesions in the corpus callosum have decreased in size and number compared with those in Figure 1. However, new punctate hyperintense lesions appeared in the cerebral cortex (arrows).
C, Axial DWI also reveals the scattered hyperintense lesions in the cerebral cortex (arrows).
On the third MR examination, performed about 2 weeks after the second examination (10 weeks after initial onset of symptoms), cortical lesions had obviously decreased in number. However, the questionable, tiny lesions in the posterior limbs of the internal capsules had increased in size and signal intensity. In addition, T2-weighted and FLAIR images showed multiple, small lesions in the thalami, posterior limbs of the internal capsules, corpus callosum, cerebellar hemispheres, and dentate nuclei (Fig 3A and B). These new lesions could not be clearly identified on T1-weighted images. DWIs showed three lesions in the corpus callosum and one in the right caudate head (Fig 3C). The latter was not depicted on either FLAIR or T2-weighted images.
Patient 1. Third MR examination at 2 weeks following relapse of the symptoms (10 weeks from initial onset).
A and B, Axial FLAIR images show multiple hyperintense lesions in the basal ganglia and thalami bilaterally, as well as in the left cerebellar peduncle and left dentate nucleus. A questionable small lesion is seen in the cortex (arrow in A).
C, Axial DWI shows a hyperintense lesion in the right caudate head (arrow), which was not depicted by either FLAIR or T2-weighted images (not shown).
The fourth MR examination, 8 months after initial onset of symptoms, showed volume loss with increased prominence of sulci and ventricles (Fig 4). Diffuse, scattered hyperintensities persisted on T2-weighted and FLAIR images, though they were fewer in number and decreased in size. No lesions were detected on DWIs.
Patient 1. Fourth MR examination at 8 months from the onset of symptoms. Axial FLAIR image shows diffuse, bilateral, confluent increased signal intensity in the deep white matter. Note the enlarged ventricles and mildly prominent sulci; this is consistent with cerebral atrophy.
Patient 2.—
On the initial MR examination, performed 2 weeks after onset of symptoms, T2-weighted and FLAIR images showed several small lesions scattered in the white matter and the cerebellar hemisphere. Seven cortical lesions depicted on DWIs were not found on either FLAIR or T2-weighted images. On the second and third MR examinations, when clinical symptoms recurred, the number of lesions increased, and new lesions appeared in the corpus callosum and basal ganglia. The fourth MR examination was performed 11 months after the first. The patient had worsening of symptoms, and the number of lesions in the white matter, cortex, basal ganglia, and cerebellum increased dramatically. The ventricles also enlarged slightly, suggesting the development of mild brain atrophy. Diffuse leptomeningeal enhancement was noted. Tables 2 and 3 summarize the distribution and number of lesions on the serial MR examinations, respectively.
Distribution and number of lesions detected at serial MR studies in patient 1
Distribution and number of lesions detected at serial MR studies in patient 2
ADC Values of Lesions
ADCs were calculated for 65 lesions, which were detected as hyperintensities on DWIs in both patients. These values were compared with mean ADC values from corresponding anatomic regions in 16 control subjects, in whom the mean ADCs were 6.60–7.70 × 10−4mm2/s for one imaging unit (GE Medical Systems) and 6.98–7.84 × 10−4mm2/s for the other (Siemens).
In addition to the results described next, 45 cortical lesions were also measured in the two patients (32 in patient 1 and 13 in patient 2). Most of these lesions had increased ADC values, which might have been inaccurate because of partial-volume effects with the CSF.
Patient 1.—
Of the 19 lesions measured on the first examination, four (two in the corpus callosum, one in the white matter, and one in the cerebellar hemisphere) had restricted ADCs (5.29–6.71 × 10−4mm2/s) with z-scores <−2, three (all in the corpus callosum) had elevated ADCs (9.55–9.76 × 10−4mm2/s) with z-scores >2, and 12 (six in the corpus callosum, three in the basal ganglia, one in the white matter, and two in the cerebellar hemisphere) had ADCs in the normal range with z-scores <2 and >−2. Of the 13 lesions measured on the second examination, 11 (eight in the corpus callosum and three in the white matter) had elevated ADCs (8.58–13.50 × 10−4mm2/s), and two had ADCs in the normal range (one in the basal ganglia and one in the white matter). Among the four lesions measured on the third examination, two (one in the corpus callosum and one in the basal ganglia) had restricted ADCs (5.45 and 6.91 × 10−4mm2/s), one (in the corpus callosum) had elevated ADCs (9.86 × 10−4mm2/s), and one (in the corpus callosum) had ADC values in normal range. On the last examination, no ADC values were measured because DWIs showed no hyperintense foci.
Patient 2.—
The 29 measured lesions included one in the cerebral white matter from the first examination, three (two in the corpus callosum and one in the basal ganglia) from the second examination, four (three in the corpus callosum and one in the right hemispheric white matter) from the third examination, and 21 (seven in the corpus callosum, five in the basal ganglia, seven in the cerebral white matter, and two in the cerebellar peduncle) from the fourth examination. No lesion had a restricted ADC value. Of the 13 lesions with elevated ADCs (8.02–10.50 × 10−4mm2/s), 12 were found on the fourth examination (three in the corpus callosum, four in the basal ganglia, and five in the white matter), and one (in the corpus callosum) was found on the second examination.
Abnormalities of NLWM
In both patients, T2-weighted and FLAIR images on the last examinations showed extensive and confluent, mildly increased signal intensity throughout the deep NLWM (Fig 4). Also on the third examination of patient 1, minimally increased signal intensity was observed near the bodies of the lateral ventricles. Mean ADC values of the NLWM were elevated on the second, third, and fourth examinations in patient 1 (8.02–8.44 × 10−4mm2/s) and on the fourth examination in patient 2 (7.92 × 10−4mm2/s). ADCs were significantly different from the mean ADCs in white matter in the control subjects (7.20 × 10−4mm2/s GE unit, 7.35 × 10−4mm2/s Siemens unit; P < .05 for both patients).
Discussion
T2-weighted MR images usually show multiple, small hyperintense lesions in patients with Susac syndrome. The lesions are predominately supratentorial, with a predilection for the corpus callosum, though they can also be found in the cerebellum and midbrain (2–5, 10–19). On the basis of the clinicopathologic findings, it is known that the gray matter is often involved in Susac syndrome (2–5, 13). However, some have reported that T2-weighted images usually show lesions, which appear mainly in the white matter because of the normally increased signal intensity of the gray matter (2) and of the CSF in the sulci; these features can prevent the differentiation of lesions in those areas. In comparison, FLAIR images are more sensitive in depicting the lesions in the gray matter (Figs 1 and 2, Tables 2 and 3) and should be included in routine examinations. In our cases, T2-weighted and FLAIR images demonstrated findings characteristic of diffuse, small hyperintense lesions. The lesions were in the supratentorial white matter and gray matter, the deep gray structures, and the cerebellum. A cluster of lesions was noted in the corpus callosum.
We found contrast enhancement in some lesions and in the leptomeninges (Fig 1E). Acute or subacute lesions and leptomeninges with enhancement have also been reported in previous articles (3, 10, 14, 16). Therefore, contrast-enhanced T1-weighted images should be used routinely in the diagnosis of Susac syndrome. Moreover, enhancing lesions and leptomeninges could be used as a guide for more accurate biopsy.
In patient 1, multiple, new cortical lesions were found shortly after symptoms relapsed; this was followed by the appearance of basal ganglia lesions about 2 weeks later (Table 2). These findings are consistent with the fact that gray matter is often involved in Susac syndrome (2–5, 13), and they also demonstrate that lesions do not always appear synchronously. The previous lesions improved or partially disappeared over time, and brain atrophy occurred by the time of the fourth examination. In patient 2, characteristic MR findings of Susac syndrome were not found initially. With disease progression, the lesions increased. The multiple lesions mainly appeared 11 months later when the symptom became worse (Table 3).
Susac syndrome often has a chronic relapsing course punctuated by frequent remissions and exacerbations for 1–2 years (3, 10, 11). Imaging findings on timely MR examination could be well correlated with changes in the clinical symptoms. The syndrome is also thought to be due to microinfarction. In nine previous cases (1–5, 13, 17), brain biopsy was performed in the cerebral gray matter and white matter or corpus callosum. Multiple microinfarctions, with sclerosis of the media and adventitia of small pial and cortical vessels, were characteristic pathologic findings. Microinfarction is attributed to arteriolar occlusions.
DWI is a useful method for depicting ischemic lesions. Many previous reports have described changes in ADC and signal intensity in ischemic lesions over time (6–9). DWI and ADC values enable a unique analysis of the lesions in Susac syndrome, which are thought to be microinfarctions. In this study, DWIs were not as sensitive as T2-weighted and FLAIR images in the overall detection of lesions in the white matter, corpus callosum, basal ganglia, and cerebellum. However, the hyperintense lesions detected on DWIs provide novel insight into the pathophysiology of the disease by enabling an evaluation of the molecular diffusion of water in these lesions. DWIs demonstrated more lesions in the cortex than did T2-weighted images. Overall, FLAIR images demonstrated more cortical lesions than did DWIs; however, on a couple of individual examinations, DWIs were superior to the FLAIR images for demonstrating cortical lesions. The clear demonstration of cortical lesions is important for diagnosis and follow-up because of the frequent involvement of the cortex in Susac syndrome.
Although microinfarctions have been pathologically documented in Susac syndrome (2–5), only six lesions in patient 1 (of 67 measured lesions in both patients) had decreased ADCs, as seen in acute or early subacute stroke. This might have been be due to a timing difference between onset of ischemia producing the lesions and the MR examination. However, no lesions had low ADC values on the second examination in patient 1 or on the fourth examination in patient 2, though both examinations were performed shortly after symptoms recurred. Accurate ADC measurement might not have been possible in some small lesions because the measured voxels might have included tissues affected or not affected by microinfarctions. Moreover, the ADCs of cortical lesions were thought inaccurate because of the likely presence of partial-volume effects with CSF. Apart from the discrepancies in ADC values between the lesions and the values expected in ischemic infarction, another observation incompatible with typical infarction was that some previous lesions could not be detected at follow-up MR imaging. Resolution of lesions was also mentioned in a previous study (10). Therefore, we cannot exclude other pathologic origins, besides infarction, that might cause the lesions of Susac syndrome. Further study is needed to elucidate the meaning of ADC changes in lesions of Susac syndrome. Although experience with DWI of Susac syndrome is limited at this point, attention to the ADC changes may be helpful in determining the stage of lesions.
In both patients, T2-weighted and FLAIR images showed extensive and confluent, minimally increased signal intensity throughout the deep NLWM at 8 and 11 months after symptom onset. Moreover, ADC values became elevated over time in the NLWM. The reason is unknown. Given the presence of arteriolar occlusions in Susac syndrome, a global perfusion or oxygenation disturbance might occur with disease progression. Consequently, the white matter could be in a condition of chronic hypoxic-ischemia that leads to the changes in signal intensity and ADC values.
One limitation of this study is that the ADC changes over time could not be evaluated for specific lesions. The daily time course of ADC changes was not studied because MR examinations were not performed that frequently. Further studies in different facilities are necessary before the DWI features can be conclusively established in Susac syndrome.
The most problematic differential diagnosis for Susac syndrome, based on MR imaging is multiple sclerosis (MS). In MS, symptoms usually appear at 20–40 years of age, with a female preponderance. MS also shows T2 hyperintensities in the corpus callosum and white matter. However, the typical findings are ovoid or oblong plaques at the callososeptal interface, with perivenular extension into the deep white matter. Moreover, in contrast with lesions in Susac syndrome, which commonly involve the cortex (2–5, 10, 12–14), cortical MS plaques are rarely identified with MR imaging (20). Most MS plaques demonstrate increased diffusion on DWI. Rarely, the lesions have restricted diffusion (21). A minority of lesions in Susac syndrome have restricted diffusion; however, in our experience, restricted diffusion is seen in a greater proportion of Susac lesions than in MS plaques. If MR images in a patient with encephalopathy show multiple lesions of the corpus callosum and cerebral cortex, Susac syndrome should be included in the differential diagnosis, especially when the lesions demonstrate restricted ADC values.
In summary, we present serial brain MR findings in two patients with Susac syndrome. To our knowledge, this is the first study in which DWI and lesional ADC changes were evaluated in patients with Susac syndrome. Although the imaging appearance and ADC values in lesions were mixed and nonspecific, we think that DWI is useful in demonstrating the heterogeneous nature of the lesions, depicting occult abnormalities in the white matter, in elucidating the underlying pathologic processes, and in conducting patient follow-up. Our findings suggest that some lesions in Susac syndrome may not represent areas of microinfarction, as detected pathologically. This possibility is based on the finding of a few lesions with restricted diffusion, even when a patient is promptly imaged in relation to symptom recurrence. Further study is needed to establish the time course of ADC changes and to interpret the pattern of changes.
Footnotes
Presented at the 41th annual meeting of the American Society of Neuroradiology, Washington, DC, April-May 2003.
References
- Received June 30, 2003.
- Accepted after revision October 6, 2003.
- Copyright © American Society of Neuroradiology
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