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Where’s the Lesion? Neuroscience Core Lecture Series 23 October 2002 David Roman Renner, MD Department of Neurology Scott’s CC: “My balance is off.” Multiple ER visits for fall-related trauma “I’m losing the fine control of my fingers.” Loss of manual dexterity “I’ve had pneumonia three times.” Dysphagia to liquids>solids All of Scott’s Complaints Sounded Neurologic in Origin His lesion should lie somewhere in the neuraxis. Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Off the Top of my Head . . . Imbalance = Cerebellum Pneumonia = Brainstem (related dysphagia) Loss of Dexterity = Peripheral Nerve Neurologic Examination Higher Cortical Function Cranial Nerves Cerebellar Function Motor Sensory Deep Tendon Reflexes Pathologic Reflexes The Neuro Exam Should Evaluate the Entire Neuraxis Higher Cortical Function: cortex Cranial Nerves: subcortex, brainstem Cerebellar Function: cerebellum Motor: motor homonculous, subcortical pyramidal tracts, BS, cord, radicle, PN, muscle Sensory: ascending tracts, thalamus, subcortical tracts, sensory hononculous Deep Tendon Reflexes: afferent PN, radicle, cord, efferent PN, muscle Pathologic Reflexes: Scott’s Exam Showed: Higher Cortical Function: normal Cranial Nerves: oropharyngeal dysarthria Cerebellar Function: hypotonia, assynergy, dysmetria, staccato dysarthria, intention tremor, appendicular ataxia Motor: hypotonia, normal strength Sensory: decreased vibration and temperature Deep Tendon Reflexes: areflexia Pathologic Reflexes: plantar flexing So Where’s the Lesion? Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Cortical Brain Depends upon hemispheric dominance Non-neurologists generalize: right: visual/spatial, perception and memory left: language and language dependent memory Look for aphasias, apraxias, and agnosias Neurologic Examination when Cortical Brain is Lesioned Higher Cortical Function: aphasia, apraxia, agnosia Cranial Nerves: normal Cerebellar Function: normal Motor: weakness if you hit the motor homonculous Sensory: sensory abnormalities if you hit the sensory homonculous Deep Tendon Reflexes: hemi-hyper-reflexia Pathologic Reflexes: possibly Babinski’s reflex or frontal release signs Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Subcortical Brain Deep white radiating fibers produce equal involvement of face/arm/leg weakness sensory abnormalities Visual radiating fibers are interrupted: deep parietal: pie on the floor deep temporal: pie in the sky Neurologic Examination when Subcortical Brain is Lesioned Higher Cortical Function: normal Cranial Nerves: visual field cuts Cerebellar Function: usually normal Motor: weakness in face=arm=leg, UMN Sensory: sensory abnormalities in face=arm=leg Deep Tendon Reflexes: hemi-hyper-reflexia Pathologic Reflexes: Babinski’s reflex and possibly frontal release signs Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Brainstem The Brainstem is basically spinal cord with embedded cranial nerves, producing the following abnormalities cranial nerve abnormalities classic spinal cord complaints bowel and bladder problems long tract signs: (bilateral and crossed) corticospinal (pyramidal): motor spinothalamic: pain/temp to the thalamus dorsal columns: prioprioception/vibration to thal. Neurologic Examination when Brainstem is Lesioned Higher Cortical Function: normal Cranial Nerves: III, IV, VI: diplopia V: decreased facial sensation VII: drooping VIII: deaf and dizzy IX, X, XII: dysarthria and dysphagia XI: decreased strength in neck and shoulders Cerebellar Function: normal Motor: hemi-paresis, UMN Sensory: hemi-dysesthesias Deep Tendon Reflexes: hemi-hyper-reflexia Pathologic Reflexes: Babinski’s reflex Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Cerebellar Function Some people believe that one can not test specifically for cerebellar abnormalities no one test on examination reliably evaluates the cerebellum H: A: N: D: S: T: hypotonia assynergy of (ant)agonist muscles nystagmus dysmetria, dysarthria stance and gait tremor Neurologic Examination when the Cerebellum is Lesioned Higher Cortical Function: normal Cranial Nerves: normal Cerebellar Function: nystagmus staccato dysarthria (abnormality of prosody) Motor: hemi-hypotonia intention > positional tremor axial instability with dysmetria Sensory: normal Deep Tendon Reflexes: normal Pathologic Reflexes: none Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Spinal Cord Sensory level (horizontal) Weakness below the lesion (paraparesis) UMN signs below the lesion Bowel and bladder incontinence Neurologic Examination when the Spinal Cord is Lesioned Higher Cortical Function: normal Cranial Nerves: normal Cerebellar Function: normal Motor: weakness below the lesion Sensory: horizontal level Deep Tendon Reflexes: hyper-reflexia below the lesion Pathologic Reflexes: Babinski’s reflex Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Root/Radiculopathy Pain is the hallmark of a radiculopathy Sensory abnormalities in a dermatome provocative maneuvres exacerbate the pain Weakness in a myotome (assymetric) LMN findings Neurologic Examination when a Root is Lesioned Higher Cortical Function: normal Cranial Nerves: normal Cerebellar Function: normal Motor: assymetric weakness in a myotome Sensory: pain and dysesthesia confined to a dermatome Deep Tendon Reflexes: hypo- to a-reflexia if the root carries a reflex Pathologic Reflexes: none Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Peripheral Nerve (presuming nonfocality) Weakness: distal predominant Sensory Dysesthesias: distal predominant Neurologic Examination with Diffuse PN Lesioning Higher Cortical Function: normal Cranial Nerves: normal Cerebellar Function: normal Motor: weakness is distal predominant Sensory: dysesthesias are distal predominant Deep Tendon Reflexes: loss of distal reflexes Pathologic Reflexes: mute responses to plantar stimulation Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Neuromuscular Junction Fatiguability is the hallmark Weakness: proximal and symmetric exacerbated with use, recovers with rest often affects facial muscles (ptosis, dysconjugate gaze, slack jaw) Sensation: preserved Neurologic Examination in Disorders of the NMJ Higher Cortical Function: normal Cranial Nerves: fatiguabile ptosis, dysconjugate gaze, slack jaw Cerebellar Function: normal Motor: fatiguable proximal weakness in both UE’s and LE’s Sensory: normal Deep Tendon Reflexes: normal Pathologic Reflexes: none Divisions of the Neuraxis Cortical Brain Subcortical Brain Brainstem Cerebellum Spinal Cord Root Peripheral Nerve Neuromuscular Junction Muscle Muscle Weakness of proximal arm and leg muscles symmetric Sensation is normal though patients complain of cramping and aching Neurologic Examination in Disorders of Muscle Higher Cortical Function: normal Cranial Nerves: ptosis, dysconjugate gaze, dysphagia, dysphonia, (dysarthria) Cerebellar Function: normal Motor: proximal weakness in both UE’s and LE’s, atrophy and fasiculations, hypotonia Sensory: normal Deep Tendon Reflexes: preserved until late in the disease Pathologic Reflexes: none Scott’s Lesion Localizes to: Almost exclusively the Cerebellum, though to a minor degree the BS and PN are involved. Isolated heritable cerebellar dysfunction is rare, so we would expect to see other parts of the CNS involved. SpinoCerebellar Ataxia (SCA4) Prior to Scott’s diagnosis, his cousin was the proband for this entity. Scott has a 38-family member, 5 generation pedigree of this disorder His family entered into a study, and his family led to the classification of SCA4: ataxia with axonal sensory neuropathy