Laryngoscope Investigative Otolaryngology (Aug 2024)
Gray‐tone appearances on 4‐hour delayed gadolinium‐enhanced magnetic resonance imaging indicate severe inner ear pathology and symptoms in sudden sensorineural hearing loss
Abstract
Abstract Objective Hybrid of reversed image of positive endolymph signal and negative image of perilymph signal (HYDROPS) in delayed gadolinium‐enhanced magnetic resonance imaging (MRI) typically depicts normal inner ear as “white‐tone” and endolymphatic hydrops as “black‐transparent” appearances, whereas ears with auditory and vestibular disorders are occasionally depicted as “gray‐tone.” This study aimed to investigate the pathological basis of sudden sensorineural hearing loss (SSNHL) patients with “gray‐tone” appearances on HYDROPS. Methods Delayed gadolinium‐enhanced MRI examinations were conducted on 29 subjects with unilateral SSNHL. We mainly analyzed positive perilymph image (PPI) and positive endolymph image (PEI), which were components HYDROPS. Results On PPI, signal intensity (SI) values extracted from the cochlear and vestibular region of interest (ROI) were higher in the SSNHL ears with dizziness/vertigo symptom at the first visit compared to the healthy ear. Additionally, the PPI/PEI enhancement pattern in the vestibule was associated with a high prevalence of hearing and vestibular deteriorations at the first visit and poor hearing improvement after treatment. Conclusion Enhancement on PPI/PEI may result from leakage of gadolinium into the inner ear following breakdown of the blood‐labyrinth barrier, with high SI being correlated with the amount of leakage. Particularly, a significant leakage into the endolymphatic space, defined as PPI+/PEI+, indicates severe inner ear pathology. Ultimately, we emphasize that the “gray‐tone” appearance in the inner ear on HYDROPS comprises enhancements on both PPI and PEI and propose a new classification for evaluating SSNHL Peri‐ and Endolymphatic image Enhancement pattern in Delayed gadolinium‐enhanced MRI (SPEED). Level of Evidence 4.
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