2. Anatomy
ā¢ Limits
ā¢ Anteriorly ā Central Sulcus
ā¢ Posteriorly
ā¢ Parieto-occipital sulcus superiorly
ā¢ Preoccipital notch inferiorly
ā¢ Inferiorly ā Sylvian fissure
ā¢ Parts
ā¢ Two sulci
ā¢ Post-central sulcus
ā¢ Interparietal sulcus
ā¢ Inferior Parietal Lobule
ā¢ Supramarginal Gyrus (Area 40)
ā¢ Angular Gyrus (Area 39)
ā¢ Superior Parietal Lobule
ā¢ Bound by the post central gyrus,
interparietal gyrus and extends
onto the medial surface (areas 5
and 7)
ā¢ Post central gyrus
ā¢ Brodmans areas 1, 2 and 3
3.
4. Brodman Areas In the Parietal Lobe
ā¢ Area 1, 2 and 3 ā Postcentral Gyrus
ā¢ Primary sensory cortex
ā¢ Area 5 ā Somatosensory association
cortex
ā¢ Area 7 ā Somatosensory association
cortex
ā¢ Together form the superior parietal
lobule
ā¢ Area 39 ā Wernickeās area ā Angular
Gyrus
ā¢ Area 40 ā Supramarginal Gyrus
5.
6. Unilateral Parietal Lobe Disease
ā¢ On either side
ā¢ Cortical Sensory syndrome
ā¢ Sensory extinction
ā¢ Homonymous hemianopia with visual inattention
ā¢ Contralateral neglect
ā¢ Abolition of optokinetic nystagmus to one side
8. Cortical Sensory Syndrome
ā¢ Loss of position sense and passive movement sense
ā¢ Inability to localize touch, temperature or pain
ā¢ Astereognosis
ā¢ Agraphesthesia
ā¢ Loss of two-point discrimination
ā¢ Easy fatigability of sensory perceptions
ā¢ Difficulty in distinguishing simultaneous stimulations
ā¢ Hyperpathia
ā¢ Touch hallucinations
ā¢ Preservation sensations ā Pain, Pressure, Touch, Temperature, Vibration
(when the postcentral gyrus is not involved in the lesions)
9. Exceptions
ā¢ Cortical lesion presenting as a thalamic syndrome
ā¢ Dejerine and Mouzonās sensory syndrome
ā¢ touch, pressure, pain, thermal, vibratory, and position sense are lost on one
side of the body or in a limb
ā¢ Typically seen with thalamic lesions
ā¢ May occur with acute lesions involving the central and subcortical region of
the parietal lobe
ā¢ Cortical lesion presenting as radiculopathy or peripheral neuropathy
ā¢ May be cause by smaller lesions ā glancing blows to the skull
ā¢ Pseudothalamic Pain Syndrome
ā¢ Pain on the side deprived of sensations
10. Character of Parietal Sensory Defects
ā¢ Easy fatigability
ā¢ Inconsistent response to stimuli
ā¢ Tactile extinction ā disregard of stimuli on affected side when both
sides are stimulated simultaneously
ā¢ Hyperpathia
11. Anton Babinski Syndrome
ā¢ Anosognosia (anos- disease, agnosia ā lack of knowledge)
ā¢ Apathy
ā¢ Allocheria
ā¢ Dressing apraxia
ā¢ Extinction
ā¢ Contralateral visual field inattention
12. ā¢ Anosognosia
ā¢ Lesion lies in the cortex and white matter of Superior Parietal lobule
ā¢ Rarely lesion of ventrolateral thalamus and adjacent parietal lobe white matter may
show similar symptoms
ā¢ Unilateral Astomatognosia is more often associated with Nondominant lesions than
with Dominant parietal lesions
ā¢ In respect to spatial attention, the right parietal lobe is truly dominant
ā¢ Unilateral Spatial Neglect
ā¢ Ask the patient to draw a clock, copy a flower
ā¢ Rejection Behaviour
ā¢ Loss of exploratory and orienting behaviour with the contralateral arm
ā¢ Tendency to avoid tactile stimuli
ā¢ Release of grasp reflex ā
ā¢ Frontal ā self grasp not present
ā¢ Parietal ā self grasp present
13.
14. Motor disturbances with parietal lobe lesions
ā¢ Mild hemiparesis ā significant contribution to the corticospinal tract
ā¢ May simulate a hemiplegia because of inability to move the limb
ā¢ Reduced movements of opposite side ā Parietal lesions have been
reported to cause contralateral muscular atrophy and trophic skin
changes
ā¢ Optic ataxia ā inability to grasp an object under visual guidance
ā¢ Pseudocerebellar syndrome ā intention tremor and incoordination
ā¢ Pseudoathetosis ā random finger movements in an outstretched
hand
ā¢ Apraxias
15. Apraxia
ā¢ Loss of the ability to execute previously learned activities in the
absence of weakness, ataxia, sensory loss, or extrapyramidal
derangement that would be adequate to explain the deficit.
ā¢ Planned or commanded action is normally first conceptualized in the
parietal lobe of the language-dominant hemisphere, where visual,
auditory, and somesthetic information is integrated ā The space-time
plan
16. Apraxia
ā¢ Ideational apraxia ā What to do?
ā¢ The failure to conceive or formulate an action to command
ā¢ Areas 5 and 7 in dominant parietal lobe + supplementary and premotor cortex of bilateral
frontal lobe
ā¢ Ideomotor apraxia ā How to do?
ā¢ Impaired performance of skilled motor acts despite intact sensory, motor, and language
function.
ā¢ Patient may know how to do a task but is unable to execute it.
ā¢ Oral-buccal-lingual apraxia
ā¢ Inability to carry out facial movements on command
ā¢ May be able to imitate them
ā¢ Left supramarginal gyrus or the left motor association cortex
ā¢ Limb-kinetic apraxia
ā¢ Clumsiness due to inability to fluidly connect the various movements of the hand or limbs.
17. Apraxia
ā¢ The exact lesion - Variable
ā¢ Supramarginal gyrus
ā¢ Superior parietal lobe (areas 5 and 7)
ā¢ Subcortical or cortical
ā¢ Majority of lesions ā Left hemisphere
18. Testing for Apraxia
1. Observe the actions of a patient while he engages in simulated
tasks
2. Ask he patient to carry out symbolic acts
ā¢ Wave goodbye
ā¢ Salute
ā¢ Blow a kiss
3. Ask the patient to imitate such acts if he cannot perform them on
command
4. Ask him to do more complex tasks ā simulate taking out comb from
pocket and comb hair, brush teeth, hammer a nailā¦
19. Gerstmann Syndrome
ā¢ Left-Right Confusion
ā¢ Dysgraphia
ā¢ Finger agnosia
ā¢ Acalculia
ā¢ Lesion in inferior parietal lobule ā angular gyrus and subjacent white
matter
ā¢ Spatial knowledge mediated by the language has been proposed as a
basic underlying deficit
20. ā¢ The right angular gyrus clearly participates in visuospatial processing,
and damage to it results in severe hemi-spatial neglect.
ā¢ The left angular gyrus participate in calculation abilities, reading/
writing, naming, and some type of body-knowledge (somatognosis).
21. Visual Disorders in Parietal Lobe Lesion
ā¢ Visual Field Defects
ā¢ Homonymous hemianopia
ā¢ Homonymous inferior quadrantanopia
ā¢ Visual neglect
ā¢ Posterior parietal lesions
ā¢ More prominent on the right side
ā¢ Loss of optokinetic nystagmus
ā¢ Abolished when following objects towards the lesion side
22. ā¢ Posterior Parietal Lesions
ā¢ Deficits in localization of visual stimuli
ā¢ Inability to compare the sizes of objects
ā¢ Failure to avoid objects when walking
ā¢ Inability to count objects
ā¢ Disturbances in smooth-pursuit eye movements
ā¢ Loss of stereoscopic vision
ā¢ Blepharospasm
ā¢ Disinclination to open eyelids when addressed
ā¢ Intense blepharospasm precluding ocular examination
ā¢ Topographagnosia
ā¢ Patients are unable to orient themselves to abstract space
ā¢ Loss of topographical memory
23. Auditory Neglect
ā¢ Less apparent than is visual neglect
ā¢ Displacement of the direction of the perceived origin of sounds
toward the opposite side
ā¢ Lesion in right superior lobule.
24. Balint Syndrome
ā¢ Visual-spatial Imperception ā Simultagnosia
ā¢ Unable to percieve more than a single object at a time
ā¢ Optic Apraxia
ā¢ Difficulty in directing gaze to an object
ā¢ Optic Ataxia
ā¢ Difficulty in reaching out to an object under vision
25. Aphasias seen with Parietal Lobe Lesions
ā¢ Wernickeās Aphasia
ā¢ Temporal, supramarginal and angular gyri
ā¢ Fluent aphasia ā neologism, lacks meaning
ā¢ No repetition
ā¢ Greatly impaired comprehension
ā¢ Transcortical Sensory Aphasia
ā¢ Similar to Wernickeās but repetition is preserved
ā¢ Lesion is near the Wernickeās area
ā¢ Conduction Aphasia
ā¢ Lesion in supramarginal gyrus or insula
ā¢ Fluent aphasia where comprehension and is preserved but repetition is lost
26. Summary
ā¢ Unilateral Parietal Lobe Syndrome
ā¢ Sensory disturbances
ā¢ Homonymous hemianopia
ā¢ Abolition of optokinetic nystagmus with target moving toward side of the
lesion
ā¢ Contralateral Hemineglect
ā¢ Dominant Parietal Lobe Lesion
ā¢ Language dysfunction (Alexia)
ā¢ Gerstmann syndrome
ā¢ Bilateral astereognosis
ā¢ Bilateral apraxia