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DWI of Cholesteatoma - AJNR News Digest
January 2014
Introduction

DWI of Cholesteatoma

Benjamin Huang

Benjamin Huang

Cholesteatomas of the middle ear and mastoid are a major cause of morbidity among patients with chronic otitis media and eustachian tube dysfunction, due primarily to their destructive potential. While surgical resection successfully eradicates disease in the majority of patients, recurrences after tympanomastoidectomy are still quite common, occurring in anywhere from 10–40% of cases.1,2 For this reason, many surgeons commonly perform second-look procedures to diagnose and address recurrent or residual disease, particularly when clinical examination and postoperative CT findings are equivocal.

Over the last decade, developments in magnetic resonance diffusion-weighted imaging pulse sequences have pointed to a shift in the paradigm for postoperative surveillance away from second-look surgery to noninvasive MR imaging. Similar to intracranial epidermoids, most middle ear cholesteatomas show characteristically high signal intensity on DWI, allowing differentiation from other processes such as granulation tissue, fibrosis, and mucoid tissue, which also frequently inhabit the postoperative middle ear. The articles featured in this month’s AJNR Digest focus on the evolution of DWI in the middle ear for detection of recurrent middle ear cholesteatoma.

The first article, by Mukherji, a case report from the May 2002 issue, is included largely for historical interest, as it was among the earliest published reports on the potential utility of DWI (in this case, echo-planar DWI) for detecting cholesteatoma, and the first to demonstrate the ability of DWI to distinguish recurrent cholesteatoma from granulation tissue after mastoidectomy. Only a month later, Fitzek et al3 reported in the Journal of Magnetic Resonance Imaging that DWI was able to prospectively identify 13 of 15 surgically proven cholesteatomas, while excluding cholesteatoma correctly in 10 of 12 patients with acute otitis media and in 100% of healthy volunteers. Over the next several years, a number of studies published in both the radiology and ENT literature showed similar results, with DWI demonstrating sensitivities of 77–86% and a specificity of 100% for diagnosing residual or recurrent cholesteatoma postoperatively.4-6

The second article included in this month’s Digest was among the first to compare DWI with delayed postcontrast imaging (DPI), an alternative MR method for cholesteatoma evaluation first described by Williams et al in 2003.7 In their report, Venail et al found that the two techniques performed comparably for cholesteatomas over 5 mm in size, but that the DWI sequence they utilized (again EPI DWI) was much less sensitive when smaller cholesteatomas were included.

Common to the early studies thus far mentioned was their use of a single-shot EPI DWI sequence, which is used primarily in neuroradiology for stroke imaging. In the middle ear, however, EPI sequences suffer from poor intrinsic spatial resolution and significant susceptibility artifacts at air-bone interfaces, limiting sensitivity for detecting small mural cholesteatomas. Because of these shortcomings, alternative non-EPI DWI pulse sequences soon entered the picture. The next three articles in this month’s Digest nicely illustrated the advantages of these techniques over EPI DWI. Although these sequences vary slightly from manufacturer to manufacturer, non-EPI spin-echo DWI sequences all utilize a 180º refocusing pulse for each measured echo, which significantly reduces susceptibility artifacts at the skull base.

De Foer and colleagues were among the earliest to utilize single-shot turbo spin-echo DWI, which is the technique we use at our own institution (ie, HASTE DWI), while the research by Dremmen et al and Lehmann et al utilized multishot acquisitions—the latter study utilizing a rotating k-space acquisition scheme (PROPELLER). The study by Lehmann and colleagues was also the first, and thus far only, to have directly compared the diagnostic accuracy of a non-EPI DWI sequence with EPI DWI (in this

case, on a 3T unit), finding that PROPELLER DWI had a substantially higher sensitivity and slightly better specificity than EPI DWI, which seems to be in general agreement with what has thus far been suggested in the literature. In addition, Lehmann et al also found PROPELLER DWI to be superior to DPI. De Foer et al8 reported similar superiority of single-shot TSE DWI over DPI the following year.

The final article included this month is an excellent review of the state of DWI imaging for cholesteatoma evaluation by Schwartz and colleagues, which summarizes and contrasts the currently available techniques mentioned above as well as BLADE DWI, a technique that acquires k-space data in a radial fashion similar to PROPELLER DWI.

Despite the promise shown thus far by DWI for postoperative cholesteatoma evaluation, the question remains: Is DWI ready to completely replace second-look surgery? The answer to that question is still up for debate. While non-EPI DWI techniques appear to have significantly improved upon the early EPI DWI sequences, they still, on average, have a false-negative rate of around 15%,9 which some would consider unacceptably high. Nonetheless, it is not a stretch to believe that with continued pulse sequence improvements and increasing familiarity with the technique, DWI of the middle ear may eventually make the practice of planned second-look middle ear surgery a thing of the past.

References

  1. Shelton C, Sheehy JL. Tympanoplasty: review of 400 staged cases. Laryngoscope 1990;100:679–81. doi: 10.1288/00005537-199007000-00001
  2. Darrouzet V, Duclos JY, Portmann D, et al. Preference for the closed technique in the management of cholesteatoma of the middle ear in children: a retrospective study of 215 consecutive patients treated over 10 years. Am J Otol 2000;21:474–81
  3. Fitzek C, Mewes T, Fitzek S, et al. Diffusion-weighted MRI of cholesteatomas of the petrous bone. J Magn Reson Imaging 2002;15:636–41. doi: 10.1002/jmri.10118
  4. Aikele P, Kittner T, Offergeld C, et al. Diffusion-weighted MR imaging of cholesteatoma in pediatric and adult patients who have undergone middle ear surgery. AJR Am J Roentgenol 2003;181:261–65. doi: 10.2214/ajr.181.1.1810261
  5. Stasolla A, Magliulo G, Parrotto D, et al. Detection of postoperative relapsing/residual cholesteatomas with diffusion-weighted echo-planar magnetic resonance imaging. Otol Neurotol 2004;25:879–84
  6. Vercruysse JP, De Foer B, Pouillon M, et al. The value of diffusion-weighted MR imaging in the diagnosis of primary acquired and residual cholesteatoma: a surgical verified study of 100 patients. Eur Radiol 2006;16:1461–67. doi: 10.1007/s00330-006-0160-2
  7. Williams MT, Ayache D, Alberti C, et al. Detection of postoperative residual cholesteatoma with delayed contrast-enhanced MR imaging: initial findings. Eur Radiol 2003;13:169–74. doi:
  8. De Foer B, Vercruysse JP, Bernaerts A, et al. Middle ear cholesteatoma: non-echo-planar diffusion-weighted MR imaging versus delayed gadolinium-enhanced T1-weighted MR imaging—value in detection. Radiology 2010;255:866–72. doi: 10.1148/radiol.10091140
  9. Jindal M, Riskalla A, Jiang D, et al. A systematic review of diffusion-weighted magnetic resonance imaging in the assessment of postoperative cholesteatoma. Otol Neurotol 2011;32:1243–49. doi: 10.1097/MAO.0b013e31822e938d

 

If you were interested in this topic you may want to read these other articles:

Jindal M, Riskalla A, Jiang D, et al. A systematic review of diffusion-weighted magnetic resonance imaging in the assessment of postoperative cholesteatomaOtol Neurotol 2011;32:1243–49. doi: 10.1097/MAO.0b013e31822e938d

Mas-Estelles F, Mateos-Fernandez M, Carrascosa-Bisquert B, et al. Contemporary non-echo-planar diffusion-weighted imaging of middle ear cholesteatomasRadiographics 2012;32:1197–13. doi: 10.1148/rg.324115109

 

Image modified from: Lehmann P, Saliou G, Brochart C, et al. 3T MR imaging of postoperative recurrent middle ear cholesteatomas: value of periodically rotated overlapping parallel lines with enhanced reconstruction diffusion-weighted MR imaging.