Abstract
SUMMARY: Diagnosis of acquired middle ear cholesteatoma on MR imaging is mostly done on late postgadolinium T1-weighted MR images and/or echo-planar (EPI) diffusion-weighted (DWI) MR images. We describe the appearance of a case of a complicated attical middle ear cholesteatoma on single-shot (SS) turbo spin-echo (TSE) DWI compared with EPI-DWI. This case suggests a higher reliability of SS TSE-DWI in the diagnosis of acquired middle ear cholesteatoma.
Diagnosis and extension of an acquired middle ear cholesteatoma is mainly done on thin-section, high-resolution CT. In selected cases, MR imaging has an additional value in describing possible complications of a middle ear cholesteatoma, such as extension to the lateral semicircular canal and other portions of the membranous labyrinth and the middle fossa through the eroded tegmen.1 Recent reports have suggested the improvement in MR imaging techniques in diagnosing cholesteatoma with the use of delayed contrast-enhanced, T1-weighted MR images2–3 and echo-planar (EPI) diffusion-weighted (DWI) MR images1,4–8 However, numerous artifacts can be generated during acquisition of DWI, such as eddy current artifacts, susceptibility artifacts, ghosting artifacts, chemical shift, and motion artifacts. With the use of higher magnetic fields, these artifacts and image distortions on EPI-DWI are even more pronounced.9–11 Turbo spin-echo (TSE) DWI MR is known to lack significant image distortions and other artifacts. It permits fast multiplanar imaging in artifact-prone regions, such as the posterior fossa and the inferior frontal and temporal lobes.12
Case Report
A 76-year-old man presented with chronic ear discharge at the otorhinolaryngology department. Otoscopic findings revealed a tympanic membrane perforation and retraction with suspicion of a partially evacuated cholesteatoma. CT of the left ear revealed a soft tissue lesion (0.8 cm) in the attic with loss of the bony delineation of the anterior limb of the lateral semicircular canal (Fig 1) and the tegmen (Fig 2). Erosion of the incus body as well as the short and long process of the incus was noted (Fig 1). MR imaging was performed for evaluation of possible invasion into the membranous labyrinth and the middle cranial fossa. MR imaging was done on a 1.5T superconductive system (Avanto; Siemens Medical Solutions, Erlangen, Germany). Imaging parameters are detailed in Table 1. Coronal thin-section, T2-weighted MR imaging revealed a slightly hyperintense nodular lesion under the tegmen delineated on its lateral side by clearly more hyperintense material (Fig 3). Late (45′) postgadolinium T1-weighted MR imaging in the coronal plane showed a small, nonenhancing lesion surrounded by enhancing material mainly on its lateral side that was strongly suspected to be an attical, nonenhancing cholesteatoma (5 mm) surrounded by enhancing inflammatory tissue (Fig 4). No enhancement was noted in the membranous labyrinth or in the middle cranial fossa. On (B1000) EPI-DWI images, a curvilinear hyperintensity under the temporal lobe was seen on both sides. A clear nodular hyperintensity suspicious for a cholesteatoma could not be noted (Fig 5). The single-shot TSE-DWI showed no curvilinear hyperintensity at the air-bone interface of the temporal bone and obviously demonstrated a small nodular hyperintensity immediately under the temporal lobe highly suggestive of a small cholesteatoma (Fig 6). On the basis of the late postgadolinium T1-weighted images and single-shot TSE-DWI, an attical cholesteatoma with surrounding inflammation without middle cranial fossa and membranous labyrinth invasion was diagnosed. Surgery confirmed the presence of a 5-mm large attical cholesteatoma surrounded by inflammation with erosion of the lateral semicircular canal but without invasion of the membranous labyrinth. The tegmen was thinned but not disrupted.
Sequence Name | Orientation | TR (ms) | TE (ms) | Section (mm) | Matrix | FOV (mm) |
---|---|---|---|---|---|---|
EPI DWI | Coronal | 3000 | 82 | 3 | 128 × 128 | 128 × 170 |
SS TSE DWI | Coronal | 2000 | 115 | 2 | 134 × 192 | 220 × 220 |
TSE T1WI | Coronal/transverse | 450 | 17 | 2 | 192 × 256 | 128 × 170 |
TSE T2-WI | Coronal | 3500 | 92 | 2 | 192 × 256 | 128 × 170 |
Note:—EPI indicates echo-planar imaging; DWI, diffusion-weighted MR imaging; SS, single-shot; TSE, turbo spin-echo; T1WI, T1-weighted imaging; T2WI, T2-weighted imaging, TR, repetition time; TE, echo time; FOV, field of view.
Discussion
Thin-section, high-resolution CT remains the primary imaging technique for the diagnosis and description of extension of a suspected middle ear cholesteatoma.1 In selected cases, MR imaging has an additional value for the evaluation of cholesteatoma extension and for the assessment of possible complications such as erosion of the lateral semicircular canal, invasion of the membranous labyrinth, and invasion of the middle cranial fossa through an eroded tegmen.1 Other complications, such as intracranial extension with temporal lobe abscess formation and facial nerve involvement can also be evaluated on MR imaging.1 MR imaging is extremely useful for the demonstration and delineation of a temporal lobe encephalocele in the case of a deficient tegmen.1 MR imaging is able to discriminate the nonenhancing cholesteatoma from enhancing inflammatory or granulation tissue.13 Several reports have discussed the appearance of acquired cholesteatoma on late postgadolinium T1-weighted MR images2,3 and on EPI-DWI images.1,4–8 On EPI-DWI, cholesteatomas demonstrate a hyperintensity probably based on a T2 shine-through effect.4,8 However, a major limitation of the EPI-DWI images still seems to be the important susceptibility artifact at the skull base (among other artifacts), the low resolution, and relatively thick sections,9–11 thus causing a size limit for detection on EPI-DWI of approximately 5 mm.5,7,8 Susceptibility artifacts caused by field inhomogeneities at the air-bone interface of the temporal bone can be reduced with the use of parallel imaging techniques.11,14 Other acquisition sequences that are less sensitive to susceptibility artifacts, such as multishot EPI sequences, spin-echo EPI sequences, and flash sequences, can be used.11
Single-shot TSE-DWI uses a 180° radio-frequency refocusing pulse for each measured echo, which explains the reduction of the susceptibility artifact. It allows the use of a higher imaging matrix and thinner sections (2 mm). Our case suggests that single-shot TSE-DWI with an actual size of 2 mm is able to discriminate smaller cholesteatomas. In this particular case, because of the absence of susceptibility artifacts at the interface between temporal lobe and temporal bone, the cholesteatoma could obviously be depicted. This demonstrates the advantage of this sequence. The size of the actual cholesteatoma at surgery was 5 mm. It was surrounded by inflammatory tissue. Furthermore, the late postgadolinium T1-weighted images also succeeded in differentiating the nonenhancing cholesteatoma from the surrounding enhancing inflammatory and granulation tissue.
Although in this case the combination of late postgadolinium T1-weighted images and single-shot TSE-DWI proved to be very convincing for the diagnosis of a primary acquired cholesteatoma, further studies on larger series are needed to prove the value of single-shot TSE-DWI in combination with late postgadolinium T1-weighted images for the diagnosis of primary acquired and residual cholesteatoma.
References
- Received December 20, 2005.
- Accepted after revision March 1, 2006.
- Copyright © American Society of Neuroradiology