AJR 2003; 180:71-75
© American Roentgen Ray Society
Diffusion-Weighted MR Imaging of Pyogenic Ventriculitis
John A. Pezzullo1,
Glenn A. Tung,
Sanjay Mudigonda and
Jeffrey M. Rogg
1 All authors: Department of Diagnostic Imaging, Brown University School of
Medicine, Rhode Island Hospital, 593 Eddy St., Providence, RI 02903.
Received February 12, 2002;
accepted after revision June 13, 2002.
Address correspondence to J. A. Pezzullo.
Abstract
OBJECTIVE. The purpose of this study was to describe the features of
pyogenic ventriculitis (ventricular empyema, pyocephalus) on
diffusion-weighted MR imaging.
CONCLUSION. Markedly increased signal intensity of dependent
intraventricular fluid on diffusion-weighted MR imaging and an apparent
diffusion coefficient that is less than that of normal cerebral white matter
indicate restricted water diffusion in purulent fluid and suggest the
diagnosis of pyogenic ventriculitis.
Introduction
Ventriculitis is a rare cerebral infection that may result from the rupture
of a brain abscess, the extension of meningitis into the ventricles, or a
neurosurgical procedure or device
[1,2,3,4].
Pyogenic ventriculitis (ventricular empyema, pyocephalus) is a subset of
ventriculitis that is characterized by the presence of suppurative fluid in
the ventricles. Pyogenic ventriculitis is important to recognize because its
signs and symptoms may be subtle, its course can be indolent but lethal, and
it may be the cause of meningitis that is difficult to eradicate
[5,6,7].
Because the incidence of bacterial meningitis has increased over the last 30
years as a result of nosocomial infection, the number of cases of pyogenic
ventriculitis is likely to increase
[7]. However, given its rarity,
the diagnosis of pyogenic ventriculitis on CT and MR imaging has not been
widely reported
[8,9,10,11].
The value of diffusion-weighted MR imaging for the diagnosis of a brain
abscess has been described in a series of case reports
[12,13,14,15].
In the purulent center of a brain abscess, water diffusion is restricted; this
finding is indicated by markedly increased signal intensity on
diffusion-weighted MR images and decreased signal intensity on apparent
diffusion coefficient map images. However, restricted water diffusion in a
rim-enhancing mass is not specific for a brain abscess
[16]. In this report, we
present three patients with pyogenic ventriculitis that were diagnosed
prospectively as a result of signs of marked restricted water diffusion on
diffusion-weighted MR imaging.
Subjects and Methods
Pyogenic ventriculitis was diagnosed prospectively in three patients during
a 5-month period from May 2001 to September 2001. All patients underwent MR
imaging of the brain. These examinations were performed on a 1.5-T magnet
(Vision; Siemens, Erlangen, Germany). Specific sequences included axial and
parasagittal spinecho T1-weighted MR imaging before and after the
administration of 0.1 mmol/kg of gadopentetate dimeglumine (Magnevist;
Schering, Berlin, Germany), axial turbo spin-echo T2-weighted MR imaging, and
fluid-attenuated inversion recovery (FLAIR) imaging.
The specific parameters for conventional spin-echo T1-weighted MR imaging
were a TR/TE of 600/14 with 3 signals acquired, 6-mm section thickness, 220
x 256 matrix, and 230 x 230 field of view. For turbo spin-echo
T2-weighted MR imaging, the parameters were a TR range/effective TE of
5000-6000/128 with 1 or 2 signals acquired, 6-mm section thickness, echo-train
length of 23, 192 x 256 matrix, and 230 x 230 field of view. For
FLAIR imaging, the parameters were a TR/TE of 9000/105, an inversion time of
2500 msec, 5-mm slice thickness, 173 x 230 field of view, 154 x
256 matrix, and an interslice gap of 2 mm.
Diffusion-weighted MR imaging was performed with an axial single-shot
echoplanar spin-echo sequence (TR/TE, 4000/110; 5-mm section thickness; 96
x 200 matrix; 230 x 230 field of view; three b values of 0, 500,
and 1000 mm2/sec). Diffusion gradients were applied in three
standard orthogonal planes to generate three sets of orthogonal trace
diffusion-weighted images. The apparent diffusion coefficient was quantified
from the mean of three circular region-of-interest measurements, each of which
was 2-3 mm in diameter, on the apparent diffusion coefficient map image.
Clinical information and laboratory data were obtained through a
retrospective review of the hospital medical records.
Results
All three patients were male: patient 1 was 14 days old; patient 2, 32
years; and patient 3, 50 years. In patient 1, a ventriculoperitoneal shunt
catheter was placed on the second day of life for management of congenital
hydrocephalus. Both patients 2 and 3 had a history of von HippleLindau
disease and presented with hydrocephalus due to compression of the fourth
ventricle by hemangioblastoma. All three patients became febrile and showed
neurologic deterioration an average of 8 days (range, 4-12 days) after
ventricular shunt placement. Results from blood tests in patients 1 and 2
revealed peripheral leukocytosis with a left shift.
In all three patients, cerebrospinal fluid obtained from the
ventriculostomy catheter was turbid and had elevated protein and reduced
glucose concentrations. In the cerebrospinal fluid of patient 1, the protein
concentration was 237 mg/dL, the glucose concentration was 3 mg/dL, and
Enterococcus faecalis was cultured. Cerebrospinal fluid from patient
2 had protein and glucose concentrations of 129 mg/dL and 26 mg/dL,
respectively, and coagulase-negative Staphylococcus aureus was
cultured. In patient 3, the protein concentration in the cerebrospinal fluid
was 85 mg/dL, the glucose concentration was 20 mg/dL, and Serratia
marcescens was cultured.
On MR imaging, intraventricular debris was shown in the dependent occipital
horn of the lateral ventricles in all patients (Figs.
1A,1B,1C
and
2A,2B,2C,2D).
Relative to cerebrospinal fluid, this debris was irregular and slightly
hyperintense on T1-weighted images, slightly hypointense on T2-weighted
images, and hyperintense on FLAIR images. Hyperintense signal was also noted
on FLAIR images in the subependymal white matter in two patients and in the
ventricular ependymal in one patient. After gadodiamide contrast medium was
administered, diffuse ependymal enhancement was noted in all three patients.
No evidence of brain abscess, meningitis, or parameningeal infection was
detected.

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Fig. 1A. 50-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma and ventricular shunt placement.
Fluid-attenuated inversion recovery image (TR/TE, 9000/105; inversion time,
2500 msec) shows ventricular debris in dependent part of occipital horns
(straight arrows) has higher signal intensity than cerebrospinal
fluid in nondependent parts of lateral ventricles. Hyperintense signal around
ventricles (curved arrow) is consistent with ependymitis and
periventricular inflammation.
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Fig. 1B. 50-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma and ventricular shunt placement.
Contrast-enhanced T1-weighted MR image (650/17) shows irregular ventricular
debris with curved and oblique layering (arrows) in occipital horns.
This nonlinear fluidfluid interface is consistent with pus. Faint
linear ependymal contrast enhancement is also present.
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Fig. 1C. 50-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma and ventricular shunt placement. Tensor
diffusion-weighted MR image (4000/110; b value, 1000 m2/sec) shows
pus in dependent position of occipital horns and marked hyperintense signal
(arrows) compared with cerebrospinal fluid and brain.
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Fig. 2A. 32-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma. Fluid-attenuated inversion recovery (FLAIR)
image (TR/TE, 9000/105; inversion time, 2500 msec) shows hyperintense debris
(arrow) in occipital horns of both lateral ventricles and
hyperintense signal around ventricles.
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Fig. 2B. 32-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma. Tensor diffusion-weighted MR image (4000/110;
b value, 1000 m2/sec) shows greater relative hyperintensity in
intraventricular pus (arrow) than on FLAIR image (A).
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Fig. 2C. 32-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma. Magnified apparent diffusion coefficient map
of left lateral ventricle shows that pus in more dependent position has lower
apparent diffusion coefficient (33.1 x 10-3
mm2/sec) than pus in more anterior, less dependent position (97.6
x 10-3 mm2/sec). Circular regions of interest are
outlined and numbered (1-4).
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Fig. 2D. 32-year-old man with purulent ventriculitis after resection
of cerebellar hemangioblastoma. In contrast to C, this image, which is
same apparent diffusion coefficient map image as that shown in C, shows
normal-appearing cerebrospinal fluid and much higher apparent diffusion
coefficient values; in addition, no position-dependent gradation is visible.
Circular regions of interest are outlined and numbered (1-4).
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In all patients, tensor diffusion-weighted imaging showed hyperintense
signal in the dependent intraventricular debris but hypointense signal in the
nondependent cerebrospinal fluid. The measured apparent diffusion coefficient
values of dependent intraventricular fluid were lower than that of
normal-appearing white matter and much lower than that of nondependent
cerebrospinal fluid in the frontal horns. The apparent diffusion coefficient
(mean x 10-3 mm2/sec ± SD) for dependent
intraventricular debris, nondependent cerebrospinal fluid, and normal white
matter was 0.44 ± 0.03, 3.16 ±0.17, and 0.75 ± 0.06,
respectively, in patient 1; 0.69 ± 0.1, 2.99 ± 0.09, and 1.09
± 0.04, respectively, in patient 2; and 0.66 ± 0.05, 3.43
± 0.17, and 0.8 ± 0.06, respectively, in patient 3. Expressed as
a percentage of normal white matter, the apparent diffusion coefficient for
dependent intraventricular debris was 57% in patient 1, 63% in patient 2, and
83% in patient 3. In addition, there was a gradation of apparent diffusion
coefficient values in dependent intraventricular debris: the smallest apparent
diffusion coefficient values were measured in the most dependent
intraventricular fluid and decreased in less dependent fluid (i.e., more
rostral in the supine patient). This gradation was not observed in
nondependent cerebrospinal fluid.
Discussion
Pyogenic ventriculitis is a rare intracranial infection that most often
occurs as a complication of brain abscess rupture into the ventricles. Fukui
et al. [11] recently described
the MR and CT imaging features of 17 patients with pyogenic ventriculitis. An
irregular configuration of ventricular debris, hydrocephalus, periventricular
hypointensity, ependymal contrast enhancement, and signs of meningitis were
reported in many, but not all, patients. In the three patients we presented,
each of these features was present with the exception of hydrocephalus, which
was absent because shunt catheters had been placed. Diffusion-weighted MR
imaging findings notwithstanding, these MR imaging signs are important because
they serve to distinguish an intraventricular hemorrhage from pyogenic
ventriculitis. In particular, periventricular hyperintensity on FLAIR images
and ependymal contrast enhancement on MR images would not be expected in cases
of intraventricular hemorrhage, and marked signal loss in blood products would
be expected on gradient-echo T2*-weighted MR imaging in cases of
intraventricular hemorrhage
[17,
18].
With respect to diffusion-weighted MR imaging findings, Fukui et al.
[11] reported that diffusion
in purulent intraventricular fluid was not restricted in two cases; however,
these researchers did not report the apparent diffusion coefficient values for
these cases. The diffusion-weighted MR images in these cases showed
hyperintense signal in the layering intraventricular debris, which may have
resulted in increased conspicuity.
We report markedly restricted diffusion in dependent purulent
intraventricular fluid in three patients with pyogenic ventriculitis. The mean
apparent diffusion coefficient, based on three region-of-interest
measurements, of intraventricular pus in each patient was less than that of
cerebral white matter, four to seven times lower than that of normal-appearing
cerebrospinal fluid, and in the range of reported values for suppurative fluid
in brain abscesses (i.e., 0.3-0.7 x 10-3 mm2/sec)
[12,13,14,15,16].
Diffusion-weighted MR imaging can be used to evaluate the composition of
fluid in brain cystic masses, and restricted diffusion has been used to
discriminate brain abscess from cystic brain neoplasm
[19]. Pus is a viscous fluid
that consists of mucoproteins, bacteria, inflammatory cells, and cellular
debris. The relatively high viscosity, hypercellularity, and binding of water
to macromolecules have been suggested as explanations for the restricted water
diffusion observed in the purulent core of a pyogenic brain abscess
[12,13,14,15,16,17,18,19,20].
We report a position-dependent reduction in measured apparent diffusion
coefficient values of intraventricular purulent fluid that was not observed
for nonsuppurative cerebrospinal fluid. When the MR images were obtained with
the patient in the supine position, the apparent diffusion coefficient was
about four times lower in pus located in the dependent posterior part of the
occipital horn than that located more anteriorly. This discrepancy in apparent
diffusion coefficient values suggests that the dilution of purulent fluid by
nonsuppurative cerebrospinal fluid may explain the slightly greater apparent
diffusion coefficient in nondependent intraventricular pus, as has been
suggested in a case reported by Rana et al.
[21]. Thus, the two cases of
pyogenic ventriculitis that were described by Fukui et al.
[11] in which the diffusion of
purulent fluid was not restricted might be explained by relatively small
amounts of intraventricular pus.
In conclusion, the finding of restricted diffusion in patients with
pyogenic ventriculitis suggests the presence of intraventricular pus. Although
an apparent diffusion coefficient value of ventricular fluid that is less than
that of normal-appearing white matter is consistent with suppuration, higher
apparent diffusion coefficient values might be observed when pus is diluted by
nonpurulent cerebrospinal fluid.
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