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URRENT
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OPINION
Purpose of review
To examine the rationale and utility of imaging in patients with known or suspected cholesteatoma, with
emphasis on high-resolution computed tomography (HRCT) and diffusion-weighted MRI (DW-MRI).
Recent findings
The initial diagnosis of cholesteatoma is largely based on patient history and clinical findings. HRCT scan
can be a useful adjunct to define the presence of pathologic soft tissue in the temporal bone, and the extent
of bony erosion, and inform the otologic surgeon about expected findings at the time of surgery. Although
MRI has not traditionally been used in the evaluation of cholesteatoma given its poor resolution of bone
anatomy, recent advances in DW-MRI sequences allow for high sensitivity and specificity in identifying the
presence of cholesteatoma. More specifically, non-echo-planar DW-MRI is superior in the detection of
residual or recurrent cholesteatoma compared to delayed-contrast MRI and echo-planar DW-MRI.
Summary
HRCT and DW-MRI offer complementary anatomic information that can be used effectively in the
management of cholesteatoma. DW-MRI imaging has proven to be a reliable method for detecting residual
or recurrent cholesteatomas down to 3 mm in size, and allows radiologic differentiation between
cholesteatoma and other soft tissue. As more centers implement DW-MRI imaging for detecting residual or
recurrent cholesteatoma, there will likely be less need for second-look surgery, thereby potentially
decreasing associated morbidity and surgical costs.
Keywords
cholesteatoma, computed tomography, diffusion-weighted imaging, magnetic resonance imaging
INTRODUCTION
Cholesteatoma has long presented otologists
with many diagnostic and therapeutic challenges.
Although cholesteatoma is usually readily identified
based on history and otoscopic examination, its
presence and extent may not always be entirely
clear. This is particularly the case in postoperative
ears, in which recurrent or residual disease may
present in areas hidden from direct examination.
The considerable variability of the size and location
of cholesteatoma can have considerable impact on
surgical approach and expectations. Similarly, the
potential involvement of vital adjacent structures
can also present hidden risks. For these reasons, the
efficient use of imaging can be a valuable adjunct
to the clinical management of these patients.
Since its introduction in the early 1980s, highresolution computed tomography (HRCT) has been
the gold standard for imaging in cholesteatoma
[13]. HRCT remains the best modality for defining
the bony anatomy, including the ossicles, delicate
bony trabeculations, patterns of pneumatization,
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KEY POINTS
HRCT scan provides a fast and reliable method for
evaluating temporal bone anatomy and provides
invaluable information for primary cases of
cholesteatoma. Useful in the postoperative period,
with high negative predictive value when it shows a
disease-free middle ear and mastoid.
DW-MRI has shown the highest sensitivity and
specificity in detecting recidivistic cholesteatoma.
Cholesteatomas of size 3 mm or larger can be detected
by DW-MRI and differentiated from granulation tissue,
scar, and fibrosis.
Low-risk patients for developing residual or recurrent
cholesteatomas can be stratified for serial DW-MRI and
potentially avoid additional surgery.
DW-MRI will likely decrease the quantities of secondlook surgeries, decreasing patient morbidity and
surgical costs. Patients may still require second-look
surgery to address reconstruction of the conductive
hearing mechanism of the middle ear.
HIGH-RESOLUTION COMPUTED
TOMOGRAPHY
With present CT scanner technology, a volumetric
HRCT of temporal bone with 0.6 mm slice thickness
(a)
(b)
can be performed in about 40 s with minimal discomfort and no need for intravenous (i.v.) contrast.
Reformatting can be performed at arbitrary planes
from the original dataset in cases in which planar
views in nonstandard orientations may be helpful.
The strength of HRCT is its ability to image
bone. A cholesteatoma appears as abnormal appearance of soft tissue, usually occurring in pneumatized
regions of the temporal bone. The normal aeration is
lost and the surrounding bone often shows evidence
of erosion with smooth or scalloped margins.
Adjacent ossicles may be absent, eroded, or demineralized. The scutum is often eroded, revealing
the pathway of ingrowth of epithelium from the
pars flaccida into the epitympanum (Fig. 1: coronal).
HRCT is also very useful in identifying the
geometry and location of adjacent vital structures.
The inner ear, facial nerve, tegmen, sigmoid sinus,
and carotid artery can all be seen quite readily on
the same sequence given their interface with bone.
A careful study of the HRCT can reveal anatomic
variations that may impact surgery. Similarly, loss
of the normal bone overlying any of these structures
may give a valuable warning of involvement by
cholesteatoma.
When ossicular or mastoid bony erosion is
seen with a soft tissue density, HRCT can identify
cholesteatoma with specificity between 8090%
[4,5]. However, HRCT has proven unreliable in
differentiating residual or recurrent cholesteatoma
from granulation tissue, cholesterol granuloma,
mucosal edema, fibrosis, scar tissue, or fluid [68].
In the postoperative period, HRCT has proven to be
a method with high negative predictive value
when it shows a well aerated middle ear with no
(c)
FIGURE 1. Cone beam computed tomography scans of a patient with left cholesteatoma. Axial (a), coronal (b), and sagittal
(c) orientations show diagnostic and therapeutic findings, including: a sclerotic mastoid with an erosive cholesteatoma (C),
demonstrating scalloped edges, scutum erosion (S) and a demineralized ossicular chain (O). The subtle flattening over the
lateral semicircular canal seen on the coronal image () is also indicative of progressive expansion. The tegmen (T) is
dehiscent and low-lying, affording minimal surgical access to the epitympanum. There is tympanosclerosis medial to the
ossicular chain (TS). The facial nerve (FN), is shown to be dehiscent adjacent to the oval window on the coronal image, and
the chorda tympani can be seen on the sagittal reconstruction. A, anterior; C, Cholesteatoma; ChT, Chorda tympani; FN,
facial nerve; L, left; O, ossicles; P, posterior; R, right; S, scutum; T, tegmen; TS, tympanosclerosis.
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MRI
Although MRI, unlike HRCT, cannot give the bony
definition that can provide a geometric framework
for surgical planning, selected MRI techniques
can provide valuable information regarding the
presence, size, and approximate location of cholesteatoma that may not be available on HRCT
imaging. MRI has the advantage of not requiring
exposure to radiation, although it does require
longer acquisition times compared to HRCT, and
the need for immobilization may make it difficult
to obtain in young children.
On traditional MRI sequences, cholesteatomas
appear dark on T1-weighted images, bright on
T2-weighted images, and do not take up i.v. contrast. This makes them indistinguishable from much
of the other soft tissue present in a chronic ear. One
mechanism to circumvent this limitation has been
through the use of delayed-contrast techniques.
Delayed-contrast MRI has been used to better detect
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(a)
(b)
FIGURE 2. (a) Axial high-resolution computed tomography (HRCT) scans of a patient with a primary left cholesteatoma,
showing soft tissue on the epitympanum (). Although this finding is consistent with cholesteatoma, it is impossible to
distinguish this from other soft tissues seen in chronic otitis media. (b) Diffusion-weighted (DW)-MRI of the same patient. Note
the bright area in the epitympanum () that corresponds to the soft tissue seen on the CT. The high signal results from restricted
diffusion of water within the keratin debris, and supports the diagnosis of cholesteatoma. This provides complementary
information to the anatomic detail seen on CT.
(a)
ear, one cannot use bone erosion to help differentiate the soft tissue from scar, fluid, or edema. This is
likely the situation in which DW-MRI is most useful
in imaging cholesteatoma.
After 912 months, most persistent cholesteatomas will be larger than 3 mm and therefore should
be apparent on DW-MRI [22 ,23,24,25 ,28 ,29,30].
A negative DW-MRI study may avoid the expense
and morbidity associated with a negative second
look. The surgeon needs to make the judgment
based on the likely area of involvement on whether
a recurrence of 3 mm or greater is unacceptably
large. In some areas, such as at the mastoid cavity,
a recurrent cyst of this size can usually be readily
resected. In other areas, such as the sinus tympani
or on the stapes footplate, a cholesteatoma of
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(b)
FIGURE 3. Axial images of a recurrent cholesteatoma (arrows) eroding the mastoid tip air cells 25 years following a prior
canal-wall-up tympanomastoidectomy. The patients tympanic cavity showed no evidence of disease on otoscopy. (a) Diffusionweighted (DW)-MRI shows a high signal lesion in the mastoid, consistent with cholesteatoma. (b) high-resolution computed
tomography (HRCT) confirms an erosive soft tissue lesion with loss of bone over the sigmoid sinus (s) and posterior fossa dura.
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(a)
(b)
FIGURE 4. Axial images of a cholesterol granuloma presenting as an expansile mastoid lesion (arrows) 6 years following
tympanomastoid surgery for cholesteatoma. (a) Diffusion-weighted (DW)-MRI showing heterogeneous high signal on a
PROPELLER DWI sequence. It is important to note that such restricted diffusion can occur in disease other than cholesteatoma,
as demonstrated here. By correlating this with the image shown in (b), the lesion is seen to have inherently high signal on
T1-weighted sequences (unlike the low signal expected for cholesteatoma), suggesting the diagnosis of cholesterol granuloma.
CONCLUSION
HRCT scan and DW-MRI have proven to be
complementary scanning modalities and reliable
methods for detecting and characterizing cholesteatoma. HRCT still provides a useful roadmap
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