Biomedical subjects
Publications and source records attributed to M C Guerzoni.
Ataxic hemiparesis is a relatively frequent clinical syndrome in which motor and cerebellar deficits on the same side are associated. A prospective study conducted on 27 patients who displayed these vascular symptoms confirms that the areas crucial to the onset of this syndrome are the capsular region (posterior limb-corona radiata) and the upper basis pontis.
We present a case of herpes zoster (HZ) with some uncommon features, namely lumbar localization and muscle weakness with a distribution different from the site of cutaneous eruptions and sensory deficits. Spread of HZ virus from sensory ganglion to anterior horn cells seems the only possible explanation of these clinical features. Urinary retention and CSF data confirm the hypothesis of HZ myelitis.
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A total of 66 patients with supratentorial ischemic infarct underwent serial CT scans in order to study the relationship between CT images and clinical evolution of the infarct. Little information of prognostic value is given by CT in patients with slight neurological deficits, whereas it enables factors with a negative influence on the prognosis to be identified in patients with moderate to severe deficits.
A right-handed patient with no family history of either neurological disorders or of left-handedness was affected by crossed aphasia due to a focal hemorrhagic lesion in the right hemisphere at the level of the basal ganglia. The CAT-scan revealed the site of the brain change. Our case is uncommon in that the aphasia. Assessed by neuropsychological tests, was associated with impairment of right functions such as visual and spatial cognition. Thus he does not fit the classic description of crossed aphasia, exhibiting instead language disorders similar to those following deep brain lesions. Various hypotheses were considered in attempting to explain the pathogenesis of our neurological data, none of which proved adequate to account for all the reported findings.
Foix-Chavany-Marie syndrome is characterized by diplegia involving the face, the pharynx, the tongue and the masticatory muscles, with automatic-voluntary dissociation due to vascular damage of both operculi. The prognosis is usually good for life expectancy. The authors describe a 46-year-old man in whom one operculum was destroyed because of a birth trauma, the other one was injured by an ischemic infarct in the territory of the middle cerebral artery. The clinical correlations to the site of the lesions are discussed. They confirm the diagnostic value of CT scan in evaluating this syndrome.
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