Ménière’s disease (MD) is a chronic condition characterised by fluctuating hearing loss, intermittent vertigo, tinnitus and aural fullness. Its anatomical and pathological counterpart is represented by endolymphatic hydrops (EH). Recent development and progress in magnetic resonance (MR) imaging techniques has enabled visualisation of EH in living human subjects using a 3 Tesla (T) scanner and gadolinium-based contrast-agent (GBCA) via intravenous (IV) or intra-tympanic (IT) administration. Data emerging from the literature about MR imaging of EH in MD patients are limited, and we therefore reviewed the most common MR imaging findings in the study of the endolymphatic space in both MD and non-MD patients.
Conte, G., Lo Russo, F., Calloni, S., Sina, C., Barozzi, S., Di Berardino, F., et al. (2018). MR imaging of endolymphatic hydrops in Ménière’s disease: Not all that glitters is gold. ACTA OTORHINOLARYNGOLOGICA ITALICA, 38(4), 369-376 [10.14639/0392-100X-1986].
MR imaging of endolymphatic hydrops in Ménière’s disease: Not all that glitters is gold
Palumbo G.;
2018
Abstract
Ménière’s disease (MD) is a chronic condition characterised by fluctuating hearing loss, intermittent vertigo, tinnitus and aural fullness. Its anatomical and pathological counterpart is represented by endolymphatic hydrops (EH). Recent development and progress in magnetic resonance (MR) imaging techniques has enabled visualisation of EH in living human subjects using a 3 Tesla (T) scanner and gadolinium-based contrast-agent (GBCA) via intravenous (IV) or intra-tympanic (IT) administration. Data emerging from the literature about MR imaging of EH in MD patients are limited, and we therefore reviewed the most common MR imaging findings in the study of the endolymphatic space in both MD and non-MD patients.| File | Dimensione | Formato | |
|---|---|---|---|
|
Conte-2018-Acta Otorhinolaryngol Italica-VoR.pdf
accesso aperto
Tipologia di allegato:
Publisher’s Version (Version of Record, VoR)
Licenza:
Creative Commons
Dimensione
196.41 kB
Formato
Adobe PDF
|
196.41 kB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


