ion of lesion
TRANSCRIPT
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Dr. Ragess
Post Graduate Resident
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Where is the lesion?
What is the lesion?
What can be done?
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1) Cognitive impairment
2) Motor weakness3) Sensory impairment4) Postural instability and
Imbalance5) Autonomic disturbances6) Abnormal movements
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Knowledge of Basic functional anatomy and
different pathways
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Cortical Brain
Subcortical Brain
Brainstem
Cerebellum Spinal Cord
Root
Peripheral Nerve
Neuromuscular Junction Muscle
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Corticospinal tract extend from UMN in motor
cortex through internal capsule, brainstem and
into spinal cord which ends at the level between
D12 and L1
Lesion involving the UMN or corticospinal tract
produce spasticity or upper motor neuron
type of findings (UMN i.e spasticity))
Lesion below the level of spinal cord produces
lower motor neuron type of findings
( LMN ie flaccidity)
All the cranial nerve nuclei in brainstem
have bicortical supranuclear control except
lower half of 7th nerve nucleus and
12 th N nucleus
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Upper motor neuron
Lesion
Lower motor neuron
lesion
Weakness Weakness
Increased tone
(Spasticity)
Decreased tone
( Flaccidity)
Brisk deep tendon reflexes Absent or diminished deep
tendon reflexes
Plantars up going Plantars down going
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Cortical Area Function
Prefrontal Cortex Problem Solving, Emotion, ComplexThought
Motor Association Cortex Coordination of complex movement
Primary Motor Cortex Initiation of voluntary movement
Primary Somatosensory Cortex Receives tactile information from the
body
Sensory Association Area Processing of multisensory information
Visual Association Area Complex processing of visual
informationVisual Cortex Detection of simple visual stimuli
Speech Center(Broca's Area)
Speech production and articulation
Wernicke's Area Language comprehension
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Hemiplegia with facial weakness of upper
motor neuron (UMN) type on the same side
Hemisensory disturbance including face on same sideAstereognosis, sensory inattention, etc.
Speech defect ( dominant hemisphere)
Visual field defect ( homonymous hemianopia)
Disorientation in time , Place , person
Memory impairment, behavior disturbance
Seizures etc.
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Either
Intellectual impairment, personality change
Urinary incontinence
Mono or Hemiparesis
Released primitive reflexes
Left Brocas aphasia
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RightParietal LeftParietal
Left sided sensory loss or neglect Right sided sensory loss or neglect
Agraphesthesia AgraphesthesiaLeft inferior quadrantinopia Right inferior quadrantinopia
Dressing apraxia Limb apraxia
Facial Agnosia
RightTemporal LeftTemporoparietal
Confusional state Agraphia
Facial agnosia Acalculia
Left superior quadrantinopia Finger agnosia
Left Right disorientation
Wernickes Aphasia
Alexia
Right superior quadrantinopia
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Visual field defects
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Hemiplegia with facial weakness of uppermotor neuron(UPN) type on the same side
Hemisensory disturbance including face on sameside
No Speech defect
Visual field defect ( homonymous hemianopia)
Extrapyramidal features including tremor, rigidity,bradykinesia or chorea
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A small stroke
there
(or there)will result in a major
deficit as the fibres are
packed close together
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Right arm weakness
Right facial weakness Dysphasia
Mild k f i h d l
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Mild weakness of right arm and leg
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, Dysphasia
Loss of right visual field
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Vertigo, Vomiting, Diplopia, Dysarthria, Dysphagia,Ataxia
Crossed hemiplegia - with cranial nerve on one side andhemiplegia on opposite side
Midbrain - Ipsilateral 3rd nerve with contralateral hemiplegiaIpsilateral cerebellar signs
Pons - Ipsilateral 6th + 7th nerve( lower motor neuron) withcontralateral hemiplegia
Ipsilateral cerebellar signIpsilateral hornors
Medulla - Ipsilateral 10th or 12th NIpsilateral cerebellar signs
Ipsilateral hornor's syndromeContralateral hemiplegia or hemianesthesia
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CervicalQuadriplegia (Spastic)Sensory loss with level in the neck or upper limbsSphincter disturbance(retention)
DorsalParaplegia (Spastic)Sensory loss (sensory level on abdomen or chestSphincter disturbance (retention)
Lumbosacral
Paraplegia (Flaccid)Sensory loss in lower limbs especially saddle area
Loss of anal sphincter tone and reflexSphincter incontinence
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Pain is the hallmark and provocativemaneuvers exacerbate the pain Sensory loss in a dermatome motor deficit confined to a particular myotome
(LMN type)
Usually No sphincter involvement
Level Function
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Level Function C1-C6 Neck flexors C1-T1 Neck extensors C3, C4, C5 Supply diaphragm (mostly C4)
C5, C6 Shoulder movement, raise arm (deltoid); flexion of elbow(biceps); C6 externally rotates the arm (supinates) C6, C7 Extends elbow and wrist (triceps and wrist extensors);
pronates wrist C7, T1 Flexes wrist C7, T1 Supply small muscles of the hand T1 -T6 Intercostals and trunk above the waist T7-L1 Abdominal muscles L1, L2, L3, L4 Thigh flexion L2, L3, L4 Thigh adduction
L4, L5, S1 Thigh abduction L5, S1, S2 Extension of leg at the hip (gluteus maximus) L2, L3, L4 Extension of leg at the knee (quadriceps femoris) L4, L5, S1, S2 Flexion of leg at the knee (hamstrings) L4, L5, S1 Dorsiflexion of foot (tibialis anterior)
L4, L5, S1 Extension of toes L5 S1 S2 Plantar flexion of foot
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Biceps
Brachioradialis
Triceps
Finger jerk
Knee jerk
Ankle jerk
C5-6
C5-6
C7-8
C8-T1
L3-4
S1
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Distal weakness (LMN type)
Distal sensory loss
No sphincter involvement
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Proximal weakness
Preserved tendon reflexes
No sensory loss No sphincter involvement
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Pure motor weakness which may involve any
skeletal muscle group Intermittent or variation in degree of
weakness during the day
Fatiguability
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Neck stiffness
Kerning's sign
Brudzinski sign
Contralateral sign
Head jolting
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