Brain : a journal of neurology
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In the syndrome of post-herpetic neuralgia (PHN), the nature of the sensory disturbance and its relationship both to the severity and cause of the pain is controversial. To address these issues, sensory mapping and quantitative thermal sensory testing was carried out four times in separate sessions on 35 subjects with established PHN. All subjects had pain affecting the torso or extremities and brush-evoked allodynia. ⋯ This implies that there is no simple relationship between loss of peripheral nerve function and spontaneous or evoked pain. Rather, the preservation of several sensory modalities in their area of maximal pain suggests that in some PHN patients, activity in primary afferent nociceptors that remain connected to both their peripheral and central targets contributes significantly to ongoing pain. Although other mechanisms are likely to contribute to the pain, the demonstrated responsivity of PHN to topical agents including local anaesthetics, capsaicin, and non-steroidal anti-inflammatory drugs, supports this proposed mechanism of pain generation.
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Comparative Study
An analysis of clinical seizure patterns and their localizing value in frontal and temporal lobe epilepsies.
The differentiation of frontal lobe epilepsy (FLE) and temporal lobe epilepsy (TLE) is a clinical problem of major theoretical and practical importance. Current electroclinical classification is based on retrospective studies of highly selected patients. When applied to the presurgical evaluation of patients, it has poor specificity. ⋯ Only one combination of different seizure types in the same patient occurred with statistical significance: absence and generalized motor seizures and pseudo generalized epilepsy. The results of this study suggest that relatively few seizures can be localized reliably on clinical grounds and that even in those seizure types where there is a statistically significant association with specific cortical areas, an important minority do not share the same associations. Analysis of the seizure evolution as well as initial symptoms may be of value in localizing some cases, but even here wide variation occurs...
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The ability to direct covert visual spatial attention to the left (LVF) and right visual field (RVF) was examined in 15 patients with mild to moderate Alzheimer's disease and 15 age- and education-matched controls using the covert orienting of visual spatial attention task (COVAT) modified to include both spatial and non-spatial cues. Subjects responded with a button press when they detected a target at a location 8 degrees to either the left or right of fixation. On 70% of trials a spatial cue was flashed at the target location before the target appeared. ⋯ The presence of subgroups of patients with Alzheimer's disease with qualitatively different COVAT performance indicates a large between-subject variability in attentional deficits in Alzheimer's disease. The presence of asymmetric attentional slowing and milder neuropsychological deficits in a subgroup of patients with Alzheimer's disease suggests that in these patients there is functional impairment of attentional areas in only one hemisphere rather than an asymmetric impairment of both hemispheres and that the neurodegenerative disease process may have been less advanced or in an earlier stage than that present in Alzheimer's disease patients with symmetric attentional performance and bilateral COVAT impairment. The preservation of asymmetric attentional slowing over time, together with the increased intra-subject variability in the magnitude of these asymmetries, suggests that asymmetrical COVAT performance represents a reliable reflection of underlying hemispheric function in Alzheimer's disease, although designation of asymmetrical attentional biases should be made on the basis of two or more sequential testing sessions.
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Using a standard protocol including MRI and magnetic resonance angiography (MRA), we studied 28 consecutive patients, all with an acute infarct in the lower brainstem. MRI patterns above and below the inferior olivary nucleus enabled identification of six topographical types of infarct: small midlateral, dorsolateral, inferolateral, large inferodorsolateral, dorsal and paramedian infarcts. Small midlateral, dorsolateral, inferolateral and inferodorsolateral infarcts were the most common types and were associated with Wallenberg's syndrome, with specific clusters and severity of neurological features in each of the four groups. ⋯ Atheromatosis was by far the most frequent stroke aetiology (72%), with intracranial vertebral artery tight stenosis or occlusion in 28% of the cases and in 75% of the cases with large inferodorsolateral infarct. Vertebral artery dissection and cardioembolism accounted each for 14% of the cases, the latter being associated with dorsal infarct. Our study shows that differences in topographical patterns of infarction in the lower brainstem probably reflect differences in aetiopathogenic mechanisms.
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The clinical differentiation of Parkinson's disease from the striatonigral degeneration (SND) type of multiple system atrophy (MSA) and Steele-Richardson-Olszewski syndrome (SRO) may be difficult. This is reflected by a 20-25% misdiagnosis rate in clinicopathological series of cases labelled as 'Parkinson's disease' in life. The caudate and putamen contain a high density of opioidergic neurons and receptors which have a close anatomical and physiological relationship with the dopaminergic system. ⋯ Corresponding figures for putamen opioid receptor binding were: none of the Parkinson's disease cases (0%); three of the SND cases (43%); and all of the SRO cases (100%). We conclude that there are differences in the pattern of opioid receptor binding in the striatum of Parkinson's disease, SND and SRO patients, as determined by [11C]diprenorphine PET. The different binding patterns may help to differentiate these akinetic-rigid syndromes in life.