1. Considering the patient’s history and physical examination, how precisely can the neurologic lesion be localized in this case?
Signs or Symptoms Weakness of RUE & RLE, mild R UMN facial weakness RUE & RLE neocerebellar signs (dysmetria, impaired finger-to-nose, heel-to-shin, dyssynergia, intention tremor, dysdiadochokinesis) |
Site of Lesion L corticospinal and corticonuclear tracts, above the lower third of the pons R cerebellar hemisphere, R SCP below (or L SCP above) the inferior midbrain, L VL nucleus of the thalamus, L thalamocortical radiations, L corticopontine tracts, L pontine nuclei |
It is difficult to localize the lesion in this case and in this syndrome. Basically, this syndrome can be caused by a fairly discrete lesion at any location where the corticospinal fibers and the neocerebellar (cortico-ponto-cerebellar) pathways lie in close approximation. The usual lesions (in a case such as this) would be in the left base of the pons, left cerebral peduncle involving the pyramidal tract in the crus cerebri and the superior cerebellar peduncle (SCP) after its decussation, and the left posterior limb of the internal capsule involving the pyramidal tract and the thalamocortical radiations and/or the frontopontine fibers.
4. The findings in this case represent a classic neurologic syndrome. What is the name of that syndrome, and what is its usual cause?
5. In general, what type of pathologic process do you think is involved in this case?
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