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NEUROLOGY 1993;43:1942
© 1993 American Academy of Neurology

Sensory syndromes in parietal stroke

Claudio Bassetti, MD, Julien Bogousslavsky, MD and Franco Regli, MD

From the Department of Neurology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

We studied 20 patients with an acute parietal stroke with hemisensory disturbances but no visual field deficit and no or only slight motor weakness, without thalamic involvement on CT or MRI and found three main sensory syndromes. (1) The pseudothalamic sensory syndrome consists of a faciobrachiocrural impairment of elementary sensation (touch, pain, temperature, vibration). All patients have an inferior-anterior parietal stroke involving the parietal operculum, posterior insula, and, in all but one patient, underlying white matter. (2) The cortical sensory syndrome consists of an isolated loss of discriminative sensation (stereognosis, graphesthesia, position sense) involving one or two parts of the body. These patients show a superior-posterior parietal stroke. (3) The atypical sensory syndrome consists of a sensory loss involving all modalities of sensation in a partial distribution. Parietal lesions of different topography are responsible for this clinical picture, which probably represents a minor variant of the two previous sensory syndromes. Neuropsychological dysfunction was present in 17 patients. The only constant association was between conduction aphasia and right-sided pseudothalamic sensory deficit. We conclude that parietal stroke can cause different sensory syndromes depending on the topography of the underlying lesion. Sensory deficits can be monosymptomatic but never present as a "pure sensory stroke" involving face, arm, leg, and trunk together.

Address correspondence and reprint requests to Dr. Julien Bogousslavsky, Department of Neurology, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

Received August 31, 1992. Accepted for publication in final form February 24, 1993.




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