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Somatosensory evoked potentials and magnetic resonance imaging in syringomyelia
Institution:1. Department of Clinical and Experimental Medicine, University of Pisa, via Savi 10, 56126 Pisa, Italy;2. Neuroradiology Unit, S.Chiara Hospital, via Roma 67, 56126 Pisa, Italy;3. Fondazione Ospedale S.Camillo, IRCCS, Via Alberoni 70, 30126 Lido Venice, Italy;4. Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, via Savi 10, 56126 Pisa, Italy;1. From the Glaucoma Division, Stein Eye Institute, David Geffen School of Medicine (M.M., L.C., V.M., J.C., K.N-M.), University of California Los Angeles, Los Angeles, California, USA;2. Department of Biostatistics, Fielding School of Public Health (E.S., R.E.W.), University of California Los Angeles, Los Angeles, California, USA
Abstract:Somatosensory evoked potentials (SEPs) to median and posterior tibial stimulation were obtained in 22 patients with syringomyelia. All patients had magnetic resonance imaging (MR) which defined the maximum transverse diameter of the syrinx as well as its longitudinal extension. SEP was abnormal in 16 (72%) patients. Median and posterior tibial SEPs were abnormal in 11 and 15 patients respectively. Both tests were abnormal in 10 patients. Ten patients showed absence of one or more central potentials (P/N13, N20, N22) and 7 patients demonstrated increased conduction times (N9–N20, P/N13–N20, N22–P40). The mean maximum transverse diameter of the syrinx was 7.5 mm in patients with normal SEPs and 16.2 mm in patients with abnormal SEPs. Abnormal SEP was observed in all 5 patients with loss of position sense, in 9 of 13 (69%) with loss of superficial pain and temperature, and 1 of 2 patients with motor deficit only. Central SEP abnormalities were observed in 3 of 5 patients with sensory deficits indistinguishable from a peripheral neuropathy and in 2 patients in the asymptomatic extremity. Three of 4 patients with syringomyelia and Chiari malformation had a normal SEP.
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