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Cholesteatoma is a benign but locally aggressive epithelial lesion lined by epithelium that continuously sheds keratin; the surrounding perimatrix contains inflammatory and enzymatic activity that drives bone erosion, making imaging crucial for assessing extent of disease
The term cholesteatoma is a medical misnomer: these are not neoplasms and do not contain cholesterol, but rather represent a chronic inflammatory condition with progressive epithelial proliferation
Acquired cholesteatoma (98% of cases) is subdivided into primary (no history of chronic otomastoiditis) and secondary; secondary disease arising from pars tensa or pars flaccida has distinct anatomic patterns of spread
DWI/ADC imaging with high b-values provides exceptional specificity for cholesteatoma diagnosis and is particularly valuable for detecting residual or recurrent disease post-operatively; this can reduce the need for second-look surgery
CT is essential for preoperative surgical planning to assess ossicular reconstruction needs and to exclude tegmen tympani perforation, while MRI excels at tissue characterization and small lesion detection
Special attention to the sinus tympani—the most hidden recess of the middle ear—is critical during imaging interpretation to avoid missing residual disease that could recur post-operatively
When reporting cholesteatoma, clearly describe the location (pars flaccida vs. pars tensa, middle ear vs. mastoid vs. external canal), the presence or absence of bone erosion (specifically document scutum, ossicles, lateral semicircular canal, facial nerve canal, and tegmen tympani integrity), note whether the lesion extends into the sinus tympani or aditus ad antrum, and confirm the DWI/ADC restricted diffusion pattern to support the diagnosis; if post-operative, explicitly state whether findings are consistent with residual versus recurrent disease.