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AN APPROACH TO
NEUROPATHY
Dr Bhupendra Shah
Asssistant Professor
B.P.koirala institute of health sciences
WHAT WE WILL DISCUSS?
• DEFINITION
• TYPES OF NEUROPATHY
• HISTORY AND EXAMINATION
• APPROACH
• INVESTIGATIONS
DEFINITION
• Functional disturbance or pathological
change in peripheral nervous system
Prevalence 2-8%
- 1/3rd genetic
- 1/3rd acquired
- 1/3rd idiopathic
Diabetes
mellitus
Inherited
Infection
&
Immune
Alcohol
TYPES OF NERVE FIBERS
(Erlanger/Gasser classification)
alpha
beta
gamma
delta
B fibers
C fibers
CLASSIFICATION OF PERIPHERAL
NEUROPATHIES
Peripheral
neuropathies
Axonopathies
Large and small
fiber
Small fiber
Myelinopathies
IS THIS PERIPHERAL NEUROPATHY ?
TYPES OF NEUROPATHIES
Generalised
Multifocal
Focal
TYPES OF NEUROPATHIES
Focal
• Entrapment Neuropathies
Multifocal
• Diabetes Mellitus
• Vasculitis
• SLE, PAN
• HIVMeralgia paresthetica
Myxedema
Rheumatoid Amyloid
Acromegaly
Hansen’s Disease
TYPES OF NEUROPATHIES
MOTOR
• GBS and CIDP
• Diphtheria and Botulism
AUTONOMIC
• Alcoholism
• Amyloidosis and DM
TYPES OF NEUROPATHIES
SENSORY
Small fiber
Leprosy
DM
Large fiber
Paraneoplastic
Cisplatin and other
chemotherapeutics
TYPES OF NEUROPATHIES
AXONAL
• Insidious
• Glove and stocking pattern
• Preservation of all DTRs
except ankle jerk
• Recovery in months to years
• More Residual deformity
• e.g- Vasculitis, Toxins,
Metabolic
DEMYELINATING
• Generally Acute
• Minimal sensory loss
• Loss of all DTRs
• Rapid recovery
• Residual deformity minimal
• e.g- GBS, CIDP
HISTORY
• Ethnicity and globalisation
• Dietary History
• Family History
• Drug History(including abused drugs)
• Concurrent systemic Illness
• Toxins exposure
• Behavioural related(HIV, Hepatitis C, Nutritional)
• Vaccination history
CLINICAL PROFILE
How patient presents in our setup?
झम्झम गर्छ
लाटो हुन्र्
हात खुट्टा पोल्र्
लुलो भयो
झत्का लाग्र्
चप्पल फु स्ककन्र्
बसेर उथ्न गाहो हुन्र्
APPROACH TO NEUROPATHY
Sensory
Motor
Autonomic
Combinations
Global Distribution
Distribution along nerves
WHAT?
WHERE?
APPROACH TO NEUROPATHY
Acute
Sub-acute
Chronic
WHEN
WHAT
SETTING?
PHYSICAL EXAMINATION
• 1st step
• PNS vs CNS
• CNS- speech, diplopia, ataxia, CN involvement/ myelopathy
bowel,bladder involvement
• Single or multiple nerve root or peripheral nerve plexus
• PNS- peripheral nerve roots vs plexus
• Fundoscopy optic pallor
- leukodystrophies and vitamin B12 deficiency
PHYSICAL EXAMINATION
• Motor examination
-fasciculations or cramps, or loss of muscle bulk
• Tone normal or reduced
• Deep tendon reflexes  reduced or absent.
• Bilateral foot drop steppage gait
• Proximal weakness inability to squat or to rise
unassisted from a chair
PHYSICAL EXAMINATION
• Orthostatic hypotension Autonomic fibers
involvement
• Respiratory rate and vital capacity GBS
• Lymphadenopathy, hepatomegaly or splenomegaly,
and skin lesions Systemic disease
• Mees' lines  Arsenic poisoning
HOW TO TEST ?
ELECTRODIAGNOSTIC TEST
• Cofirmation of presence
of neuropathy
• Small or large fiber
involved
• Motor, Sensory or
mixed
• Axonal Vs
Demyelination
ELECTRODIAGNOSTIC TEST
• Velocity of conduction
• Distal latency
• Conduction block
• Temporal dispersion
• F wave latency
NERVE BIOPSY
• If diagnosis is in doubt even after lab and
electrodiagnostic findings
• Vasculitis, Amyloid neuropathy, Leprosy, CIDP,
Inherited disorders of myelin
• Sural nerve M/C
• Superficial peroneal nerve – alternative; allows
simultaneous biopsy of the peroneus brevis muscle
• Combined nerve and muscle biopsy Vasculitis
MOSQUITO
VERSUS
ZEBRA
LEPROSY
• Tendon reflex – Preserved
• No autonomic neuropathy
LepromatousWidespread
invasion of cutaneous nerve
Tuberculoid  Patch of
superficial sensory loss
VITAMIN B12 DEFICIENCY
• Spinal cord, Brain, Optic nerve and Peripheral
nerves all affected
• Sub-acute Combined degeneration of cord
• Visual impairment Optic neuropathy
DIABETES MELLITUS
Diabetic
Ophthalmoplegia
Acute Diabetic
Mononeuropathy
Thoracoabdominal
Radiculopathy
Distal
Polyneuropathy
Multiple
Mononeuropathy and
Radiculopathy
Autonomic
Neuropathy
HYPOTHYROIDISM
Neurological endemic cretinism Proximal limb
and truncal rigid-spastic motor disorder
Myxedematous  No spastic rigidity
Loss of reflexes,loss of vibration, position and
touch
Sporadic Delayed tendon reflexes
ALCOHOLISM
• More common in our settings
• Slow and insidious progression
• Distal and symmetrical involvement
• Positive sensory symptoms
• Autonomic neuropathy coexistent
• Multi-factorial damage
THANK YOU

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