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Objective To investigate the patterns and mechanisms of audiovestibular impairments associated with intracranial hypotension. Methods We had consecutively recruited 16 patients with intracranial hypotension at the Neurology Center of Pusan National University Hospital for two years. Spontaneous, gaze-evoked, and positional nystagmus were recorded using 3D video-oculography in all patients, and the majority of them also had pure tone audiometry and bithermal caloric tests. Results Of the 16 patients, five (31.3%) reported neuro-otological symptoms along with the orthostatic headache while laboratory evaluation demonstrated audiovestibular impairments in ten (62.5%). Oculographic analyses documented spontaneous and/or positional nystagmus in six patients (37.5%) including weak spontaneous vertical nystagmus with positional modulation (n = 4) and pure positional nystagmus (n = 2). One patient presented with recurrent spontaneous vertigo and tinnitus mimicking Meniere's disease, and showed unidirectional horizontal and torsional nystagmus with normal head impulse tests during the attacks. Bithermal caloric tests were normal in all nine patients tested. Audiometry showed unilateral (n = 6) or bilateral (n = 1) sensorineural hearing loss in seven (53.8%) of the 13 patients tested. Conclusions Intracranial hypotension frequently induces audiovestibular impairments. In addition to endolymphatic hydrops and irritation of the vestibulocochlear nerve, compression or traction of the brainstem or cerebellum due to loss of CSF buoyancy may be considered as a mechanism of frequent spontaneous or positional vertical nystagmus in patients with intracranial hypotension. [ABSTRACT FROM AUTHOR]

Abstract: A 51-year-old man developed sudden vertigo, right hearing loss and dysphagia. Examination revealed right Horner syndrome, spontaneous torsional-horizontal nystagmus, right central type facial palsy, dysarthria, reduced soft palate elevation without gag reflex, left hypesthesia, right dysmetria and imbalance. Audiometry and bithermal caloric tests documented right sensorineural hearing loss and canal paresis. Brain MRI and cerebral angiography documented right lateral medullary infarction from vertebral artery dissection, without involvement of other parts of the brainstem supplied by the anterior inferior cerebellar artery (AICA). This case suggests artery-to-artery embolism as a possible mechanism of isolated vertigo or hearing loss from labyrinthine infarction. [Copyright &y& Elsevier]

Abstract: Although several papers have been published on perverted head shaking nystagmus (PHSN) associated with focal brainstem or cerebellar lesion, there are no reports of a focal pontine infarct that causes PHSN. We report a patient with focal pontine infarction who presented with sustained dizziness, limb dysmetria on the left extremity, decreased sensations to position and vibration of the left extremity, and gait imbalance. Only vestibular abnormality was downbeat nystagmus after vigorous head shakings. The maximum slow phase velocity of PHSN was 26°/s, and its duration was about 20s. This is the first report of PHSN associated with focal pontine infarction. Crossed ventral tegmental tract and velocity storage mechanism of vestibulocerebellum might be related on PHSN in this case. [ABSTRACT FROM AUTHOR]