Central nervous system involvement in n-hexane polyneuropathy demonstrated by MRI and proton MR spectroscopy
In the present report, we describe a patient with n-hexane polyneuropathy with CNS lesions using magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1H MRS).2 Case report A 51-year-old woman complained of difficulty rising up from a seated position and climbing stairs for si...
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Published in: | Clinical neurology and neurosurgery Vol. 113; no. 6; pp. 493 - 495 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-07-2011
Elsevier Elsevier Limited |
Subjects: | |
Online Access: | Get full text |
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Summary: | In the present report, we describe a patient with n-hexane polyneuropathy with CNS lesions using magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1H MRS).2 Case report A 51-year-old woman complained of difficulty rising up from a seated position and climbing stairs for six months prior to admission to our hospital. In a brainstem auditory evoked potential (BAEP) study, absolute latencies of I, III, and V were 1.66ms, 4.16ms, and 6.36ms, respectively (normal values [mean±SD]: 1.7±0.15, 3.9±0.19, and 5.7±0.25, respectively). [...]the I-III, III-V, and I-V interpeak latencies were 2.50ms, 2.20ms, and 4.70ms, respectively (normal values: 2.1±0.15, 1.9±0.18, and 4.0±0.23, respectively). Oge et al. described a central nerve conduction delay using the electrophysiological method of transcranial magnetic stimulation [5]. [...]studies using patterned visual evoked potential (pVEP), brainstem auditory evoked potential (BAEP), and somatosensory evoked potential (SEP) have suggested subclinical central nerve involvement in n-hexane neuropathy [2]. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0303-8467 1872-6968 |
DOI: | 10.1016/j.clineuro.2011.01.008 |