Detailed MR imaging assessment of endolymphatic hydrops in patients with SLC26A4 mutations. Issue 6 (December 2020)

• Record Type: Journal Article
• Authors: Tsukada, Keita; Usami, Shin-ichi
• Is Part Of: Auris nasus larynx. Volume 47:Issue 6(2020)
• Page Start: 958
• Page End: 964
• Publication Date: 2020-12
• Subjects: SLC26A4 -- 3T-MRI -- Endolymphatic hydrops -- Large vestibular aqueduct -- Endolymphatic sac; Otolaryngology -- Periodicals; Electronic journals; 616
• DOI: 10.1016/j.anl.2020.05.018
• Languages: English
• ISSNs: 0385-8146

Abstract

Abstract: Objective: Mutations in SLC26A4 represent the second most common mutations in deafness patients. The majority of patients with SLC26A4 mutations have a large vestibular aqueduct (LVA). Recently, some reports showed the presence of endolymphatic hydrops (ELH) in patients with LVA on the basis of high-resolution enhanced 3T-MRI. However, detailed evaluation has not been performed. We provide the first report on ELH in LVA patients with biallelic SLC26A4 mutations. In this study, we focused on 1) the findings of ELH in LVA patients with biallelic SLC26A4 mutations, and 2) the findings of the endolymphatic duct (ED) and endolymphatic sac (ES) by using two different gadodimide (Gd) enhancement methods. Subjects and methods: Five patients with SLC26A4 mutations underwent enhanced 3T-MRI using the intratympanic (IT) or intravenous (IV) injection of Gd for the diagnosis ELH. Results: All of the patients had ELH in at least one ear. ELH was identified in the vestibule (8/10 ears) as well as in the cochlea (7/10 ears). With regard to the ED and ES, all ears for which MRI was performed with an IT injection of Gd had black areas in the ES or VA or both; however, all of the ears receiving an IV injection had no black areas and were well enhanced. Conclusions: A majority of the patients had severe ELH in the cochleo-vestibular endolymph, with two different patterns observed in the MRI findings of the ED and ES.