Vestibular schwannoma and endolymphatic hydrops are two conditions that may present with similar audio-vestibular symptoms. The association of the two in the same patient represents an unusual  nding that may lead clinicians to errors and delays in diagnosis and clinical management of affected subjects. We discuss the case of a patient with an intrameatal vestibular schwannoma reporting symptoms suggestive for ipsilateral endolymphatic hydrops. The patient presented with  uctuating hearing loss, tinnitus, and acute rotatory vertigo episodes, and underwent a full audiological evaluation and imaging of the brain with contrast-enhanced Magnetic Resonance Imaging. Clinical audio-vestibular and radiological examination con rmed the presence of coexisting vestibular schwannoma and endolymphatic hydrops. Hydrops was treated pharmacologically; vestibular schwannoma was monitored over time with a wait and scan protocol through conventional MRI. The association of vestibular schwannoma and endolymphatic hydrops is rare, but represents a possible  nding in clinical practice. It is therefore recommended investigating the presence of inner ear disorders in patients with vestibular schwannoma and, similarly, to exclude the presence of this condition in patients with symptoms typical of inner ear disorders

ALTISSIMI, Giancarlo

CIANFRONE, Giancarlo

D'AGUANNO, VITTORIO

DE VINCENTIIS, Marco

GRECO, Antonio

LONGO, Lucia

RALLI, MASSIMO

TOMBOLINI, MARIO

TURCHETTA, Rosaria

English

Massimo Ralli

Antonio Greco

Giancarlo Altissimi

Rosaria Turchetta

Lucia Longo

Vittorio D'Aguanno

Mario Tombolini

Giancarlo Cianfrone

Marco De Vincentiis

Archivio della ricerca- Università di Roma La Sapienza

128CASE REPORT DOI: 10.5935/0946-5448.20170024International Tinnitus Journal. 2017;21(2):128-132.International Tinnitus Journal, Vol. 21, No 2 (2017)www.tinnitusjournal.comVestibular Schwannoma and Ipsilateral Endolymphatic Hydrops: An Unusual AssociationMassimo Ralli1Antonio Greco2Giancarlo Altissimi2 Rosaria Turchetta2 Lucia Longo2Vittorio D’Aguanno2Mario Tombolini2Giancarlo Cianfrone2Marco de Vincentiis21Department of Oral and Maxillofacial Sciences, Sapienza University of Rome, Italy 2Department of Sense Organs, Sapienza University of Rome, Italy Send correspondence to:Massimo Ralli Department of Oral and Maxillofacial Sciences, Sapienza University of Rome. Viale del Policlinico 155, 00186, Rome Italy, E-mail: massimo.ralli@uniroma1.itPaper submitted to the ITJ-EM (Editorial Manager System) on October 18, 2017;and accepted on October 31, 2017.AbstractVestibular schwannoma and endolymphatic hydrops are two conditions that may present with similar audio-vestibular symptoms. The association of the two in the same patient represents an unusual finding that may lead clinicians to errors and delays in diagnosis and clinical management of affected subjects. We discuss the case of a patient with an intrameatal vestibular schwannoma reporting symptoms suggestive for ipsilateral endolymphatic hydrops. The patient presented with fluctuating hearing loss, tinnitus, and acute rotatory vertigo episodes, and underwent a full audiological evaluation and imaging of the brain with contrast-enhanced Magnetic Resonance Imaging. Clinical audio-vestibular and radiological examination confirmed the presence of coexisting vestibular schwannoma and endolymphatic hydrops. Hydrops was treated pharmacologically; vestibular schwannoma was monitored over time with a wait and scan protocol through conventional MRI. The association of vestibular schwannoma and endolymphatic hydrops is rare, but represents a possible finding in clinical practice. It is therefore recommended investigating the presence of inner ear disorders in patients with vestibular schwannoma and, similarly, to exclude the presence of this condition in patients with symptoms typical of inner ear disorders.Keywords: vestibular schwannoma, endolymphatic hydrops, hearing loss, tinnitus.International Tinnitus Journal, Vol. 21, No 2 (2017)www.tinnitusjournal.com129INTRODUCTIONVestibular schwannomas (VS), also known as acoustic neuromas, are benign neoplasms originating from the Schwann cells of the eighth cranial nerve and present most frequently in subjects between 30 and 60 years1. VS have a prevalence of 1.4-2.1 in 10.000 people2,3, and represent 5% to 10% of all intracranial tumors, and 80% to 90% of neoplasms of the cerebellopontine angle4.VS presenting symptoms usually include slowly progressive sensorineural hearing loss, fullness and tinnitus associated to vestibular disorders in 16-70% of cases; balance disorders can present with acute rotatory vertigo and/or dizziness5,6. Medical history, clinical examination and routine audio-vestibular examination alone cannot diagnose VS; diagnosis must be confirmed by high-resolution Magnetic Resonance Imaging (MRI) with intravenous gadolinium-based contrast7. Along with imaging technology improvements, the number of VS diagnosis has increased including smaller schwannomas previously overlooked8. The presenting symptoms of VS can also be found in other inner ear disorders such as endolymphatic hydrops (ELH); nevertheless, inner ear disorders may be present in patients with VS9. ELH is a disorder of the inner ear characterized by episodic attacks of vertigo, tinnitus, fluctuating hearing loss, ear fullness, and progressive loss of the audio-vestibular function10.Differential diagnosis plays a central role for a correct diagnostic and therapeutic management of VS patients; at the same time, it is important not to overlook other concomitant inner ear disorders10. In this paper, we describe the case of a patient with fluctuating hearing loss, tinnitus and acute rotatory vertigo episodes, who presented an intrameatal vestibular schwannoma and a symptomatology suggestive for ipsilateral endolymphatic hydrops. CASE PRESENTATIONA 67-year-old man was admitted to the Otolaryngology Department of the Policlinico Umberto I, Sapienza University of Rome in December 2013 with a three-year history of fluctuating hearing loss in the left ear and vertigo attacks lasting 2 to 6 hours associated to intense nausea and vomiting (4-6 episodes/year). Last episode occurred one month before admission. After admission, patient underwent a complete otolaryngology examination with otoscopy, Pure-Tone Audiometry (PTA), Auditory Brainstem Response (ABR), Distorsion-Product Otoacoustic Emissions (DPOAE), Infrared Videonystagmography (IR-VNG) for spontaneous and gaze-evoked nystagmus and Fitzgerald-Hallpike caloric stimulation. Vestibular examination was completed with Cervical Vestibular Evoked Myogenic Potential (c-VEMP) and Ocular Vestibular Evoked Myogenic Potential (o-VEMP) response recording. Written informed consent was obtained from the patient for all the diagnostic and therapeutic procedures performed.The patient had a normal otoscopy; PTA showed a mild sensorineural hearing loss in the right ear with an average auditory threshold of 37.50 dB and a moderate sensorineural hearing loss in the left ear with an average threshold of 61.25 dB, more evident for mid-low frequencies. Weber test lateralized to the right at all frequencies. Speech Discrimination was in accordance with PTA; no alterations were found at ABR (Table 1); DPOAE amplitudes were reduced bilaterally with a significant reduction in the left ear compared to the contralateral ear (Figure 1). No spontaneous or gaze-evoked nystagmus was found at IR-VNG; left hyporeflexia was observed at the caloric test. The first c-VEMP complex of biphasic wave p13-n23 and the n10 response of the o-VEMP to Bone Conducted Vibration and Air Conducted Sound were normally evoked bilaterally. Audiological examination was followed by a conventional MRI of the brain with gadolinium-based contrast agent performed in the axial, sagittal and coronal planes focusing on the eight cranial nerve and cerebellopontine angle; heavily T2-weighted sequences revealed an intrameatal mass with cystic and solid components measuring approximately 7 x 4 mm on the left side consistent with vestibular schwannoma (Figure 2). During the following 30 months, the patient Table 1. Auditory Brainstem Response recording in our patient. No alterations can be seen for waveforms and latencies in both sides.I III V I-III III-V I-VRight 1.58 3.72 5.68 2.13 1.97 4.10Left 1.68 3.81 5.63 2.12 1.82 3.95Figure 1. Distorsion Product Otoacoustic Emissions (DPOAE) amplitudes were reduced bilaterally with a significant reduction in the left ear compared to the contralateral ear.International Tinnitus Journal, Vol. 21, No 2 (2017)www.tinnitusjournal.com130experienced fluctuating hearing loss in the left ear associated to acute vertigo attacks monitored over time with PTA and IR-VNG; exams documented a fluctuation of hearing threshold in the mid-low frequency range in the left ear with average auditory threshold for frequencies 500-4000 Hz of 53.75 dB in March 2013, 32.5 dB in February 2014, 45.75 in March 2015 and 61.25 in May 2016 (Figure 3). When recorded during the vertigo attack, IR-VNG showed a spontaneous left beating nystagmus. The patient also reported the onset of a stable high-pitch tinnitus in the left ear one year after initial admission to our unit.The results of the audiological evaluation during follow up led towards a diagnosis of left VS associated to an ipsilateral ELH. Diagnosis of ELH was posed according to AAO-HNS Committee on Hearing and Equilibrium classification criteria11,12 but was not confirmed radiologically due to unavailability of 3-Tesla MRI. Hydrops was treated pharmacologically with betahistine-dihydrochloride during crisis and long-term cinnarizine plus chlorthalidone associated to low sodium diet following our internal management protocol; VS was monitored over time with a wait and scan protocol through conventional MRI.Figure 2. Heavily T2-weighted Magnetic Resonance Imaging sequences in the axial (A) and coronal (B) planes revealed an intrameatal mass with cystic and solid components measuring approximately 7 x 4 mm on the left side consistent with vestibular schwannoma. Figure 3. Pure-Tone Auditory threshold for the left ear between March 2013 and May 2016. A clear sensorineural fluctuation of hearing threshold can be seen for the mid-low frequencies. A: 2013; B: 2014; C: 2015; D: 2016.International Tinnitus Journal, Vol. 21, No 2 (2017)www.tinnitusjournal.com131DISCUSSIONThe presentation of simultaneous VS and ELH on the same side in the same patient is uncommon and has seldom been described in the literature13-16. Although the two pathologies are most probably of independent origin and should be considered separate entities, presenting and ongoing symptoms may overlap and may cause an incorrect treatment of the cochlear disorder (i.e. misdiagnosis of the endolymphatic hydrops), a potential delay in VS diagnosis (i.e. postponing the execution of a MRI) or a potential misinterpretation of VS evolution (i.e. attributing symptoms to VS growth instead of inner ear dysfunction, or vice-versa)13,16-19. In such cases, it is always puzzling to attribute the vestibular symptoms to the inner ear or to the retrocochlear condition. Several studies discussed the origin (retrocochlear or cochlear) of audio-vestibular symptoms in patients with VS, suggesting that vertigo and hearing loss may also have a peripheral origin, possibly induced by tumor-related vascular alterations of the inner ear, rather than being exclusively linked to a direct pressure of the tumor on the vestibulocochlear nerves20,21. Roosli et al studied temporal bones from 32 patients with unilateral VS, finding significantly more hair cell loss, cochlear neuronal loss and decreased pure tone average when compared with the opposite ear; however, tumor size, distance from the cochlea, and nerve of origin did not correlate with structural changes found in the cochlea20. Due to the varying and fluctuating symptoms, the clinical diagnosis of ELH may be difficult22. The role of new imaging techniques is gaining importance in ELH diagnosis, since conventional MRI is unable to distinguish the endolymphatic from the perilymphatic compartments within the inner ear23. In the recent years, several efforts have been made to develop reliable imaging able to identify ELH; some inner ear imaging techniques enable visualizing morphological changes in the cochlea and the vestibulum in vivo24. Current research demonstrates the validity of Locally Enhanced Inner Ear MRI (LEIM) after intratympanic contrast agent application and 3-Tesla MRI performed with intravenous gadolinium with 3D-FLAIR sequences for the diagnosis and grading of ELH; these techniques have shown similar sensitivity to histopathological series in identifying ELH25-27. The degree of perilymphatic enhancement in 3-Tesla MRI also depend on the interval between the intravenous contrast administration and imaging. Research showed that a 4-hour delay results in greater contrast enhancement within the perilymph28,29. Jerin et al reported a case of a patient with VS and endolymphatic hydrops, in which ELH was revealed with the use of an inner ear LEIM MRI with an axial 3D Real-IR sequence; the authors recommended performing locally contrast-enhanced inner ear MRI in those cases in which an ELH is suspected14. In a study from Kentala and Pyykkö, the authors retrieved information on 127 patients with VS and 243 patients with ELH and found that 38% of the VS patients had the full triad of vertigo, hearing loss and tinnitus and vertigo mimicked that in ELH in 14% of cases19. In a recent study to verify whether vertigo in patients with VS correlates to vestibular endolymphatic hydrops, Naganawa et al studied 15 patients with unilateral VS using a non-contrast-enhanced 3D FLAIR MRI and reported vestibular hydrops in 4/15 cases; however, no significant correlation between vertigo and hydrops was found15.In our patient, the two pathological conditions coexist but are most probably unrelated. The full audiological and radiological protocol performed allowed to identify separately both cochlear and retrocochlear disorders, although the diagnosis of ELH was not confirmed by imaging due to unavailability of 3-Tesla MRI (the availability of 3-Tesla scanners is still limited in many hospitals) or, as suggested by some authors, electrocochleography30; consequently, ELH diagnosis was only based on symptoms reported by the patient over the years associated to the results of the auditory and vestibular evaluation performed initially and during follow up and to patient’s response to therapy. CONCLUSIONAlthough current literature supports the notion of a peripheral origin of vertigo in patients with small vestibular schwannomas, it is always recommended in patients with VS to also investigate possible coexisting independent inner ear disorders such as ELH, especially when a fluctuation in audio-vestibular symptoms is documented. When available, a 3-Tesla MRI performed at 4 hours post-intravenous gadolinium with 3D-FLAIR sequences or a locally contrast-enhanced inner ear MRI to detect endolymphatic hydrops may be useful to confirm ELH. At the same time, as widely documented in the literature, it is always recommended performing gadolinium contrast-enhanced MRI in patients with unilateral hearing loss and symptoms suggesting a peripheral origin to exclude retrocochlear lesions such as VS. Unfortunately, the need for a thorough neuro-otological work-up including MRI scanning can still be overlooked in the cases in which it appears to be a clear peripheral etiology for the hearing loss such as in endolymphatic hydrops.Conflicts of Interest None Source of FundingThis research received no specific grant from any funding agency, commercial or not-for-profit sectors.REFERENCES1. Stangerup SE, Caye-Thomasen P. Epidemiology and natural history of vestibular schwannomas. Otolaryngol Clin North Am. 2012;45(2):257-68.2. Propp JM, McCarthy BJ, Davis FG, Preston-Martin S. Descriptive epidemiology of vestibular schwannomas. Neuro Oncol. 2006;8(1):1-11.International Tinnitus Journal, Vol. 21, No 2 (2017)www.tinnitusjournal.com1323. Lin D, Hegarty JL, Fischbein NJ, Jackler RK. The prevalence of "incidental" acoustic neuroma. Arch Otolaryngol Head Neck Surg. 2005;131(3):241-4.4. Hart RG, Davenport J. Diagnosis of acoustic neuroma. Neurosurgery. 1981;9(4):450-63.5.Espinosa-Sanchez JM, Lopez-Escamez JA. Meniere's disease. Handb Clin Neurol. 2016;137:257-77.6. Gurkov R, Pyyko I, Zou J, Kentala E. What is Meniere's disease? A contemporary re-evaluation of endolymphatic hydrops. J Neurol. 2016;263(Suppl 1):S71-81.7. Coffey N, Torres C, Glikstein R, Al Mansoori T, Del Carpio-O'Donovan R, Patro S. Imaging findings in sensorineural hearing loss: a pictorial essay. Can Assoc Radiol J. 2017;68(2):106-15.8. Carlson ML, Link MJ, Wanna GB, Driscoll CL. Management of sporadic vestibular schwannoma. 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Vestibular schwannoma and ipsilateral endolymphatic hydrops: an unusual association

Vittorio D’Aguanno

Marco de Vincentiis

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Vestibular Schwannoma and Ipsilateral Endolymphatic Hydrops: An Unusual
            Association

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Vestibular schwannoma and ipsilateral endolymphatic hydrops: an unusual association

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