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Peripheral Neuropathy
Dr. Mohammad Tanvir Islam
Nervous System
• CNS
• PNS
Loss of function
“- symptoms”
Disturbed function
“+ symptoms”
Motor nerves Wasting
Hypotonia
Weakness
Hyporeflexia
Orthopedic deformity
Fasiculations
Cramps
The clinical response to motor nerve injury
www.neuro.wustl.edu/neuromuscular/pics/people/patients/Hands/handatrophymnd3.jpg
Loss of function
“- symptoms”
Disordered function
“+ symptoms”
Sensory
“Large Fiber”
↓ Vibration
↓ Proprioception
Hyporeflexia
Sensory ataxia
Paresthesias
Sensory
“Small Fiber”
↓ Pain
↓ Temperature
Dysesthesias
Allodynia
The clinical response to sensory nerve injury
Loss of function
“- symptoms”
Disturbed function
“+ symptoms”
Autonomic nerves ↓ Sweating
Hypotension
Urinary retention
Impotence
Vascular color changes
↑ Sweating
Hypertension
The clinical response to autonomic nerve injury
http://www.neuro.wustl.edu/neuromuscular/nother/skel.html#nosteo
The two types of peripheral neuropathies:
axonopathies and myelinopathies
Causes
Conditions causing mononeuropathy
• Acute (trauma-related)
• Chronic (nerve entrapment)
Disorders causing mononeuropathy multiplex
Acute
• Diabetes mellitus
• Multifocal motor neuropathy
• Vasculitic syndromes
Chronic
• Acquired immunodeficiency syndrome
• Leprosy
• Sarcoidosis
Causes
Conditions causing neuropathy with autonomic features
• Alcoholism
• Amyloidosis
• Chemotherapy-related neuropathy
• Diabetes
• Heavy metal toxicity
• Porphyria
• Vitamin B12 deficiency
Causes
Conditions causing painful neuropathy
• Diabetes
• Alcoholism
• Amyloidosis
• Chemotherapy (heavy metal toxicity)
• Idiopathic polyneuropathy
• Porphyria
• Paraneoplastic syndrome
Axonal & Demyelinating causes
• Axonal
• Diabetes mellitus
• Alcohol
• Uraemia
• Cirrhosis
• Amyloid
• Myxoedema
• Acromegaly
• Paraneoplastic
• Drugs and toxins
• Deficiency states
• Hereditary
• Infection
• Idiopathic
• Demyelinating
• Chronic inflammatory demyelinating
polyradiculoneuropathy
• Multifocal motor neuropathy
• Paraprotein-associated demyelinating
neuropathy
• Charcot–Marie–Tooth disease type I
and type X
In short
Inherited: e.g. Charcot-Marie-Tooth disease (HMSN)
Infectious: e.g. Leprosy
Inflammatory: e.g. Guillain Barre syndrome (AIDP)
Neoplastic: e.g. Monoclonal gammopathy
Metabolic: e.g. Diabetes
Drug: e.g. Vincristine
Toxic: e.g. Ethanol
History
• The temporal course of a neuropathy varies, based on the etiology.
• Trauma or ischemic infarction-acute, with the most severe symptoms at onset
• Inflammatory and some metabolic neuropathies have a subacute course
extending over days to weeks.
• A chronic course over weeks to months is the hallmark of most toxic and
metabolic neuropathies
History
• A chronic, slowly progressive neuropathy over many years
• Hereditary neuropathies
• Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)
• Neuropathies with a relapsing and remitting course include
• CIDP
• acute porphyria
• Refsum's disease
• hereditary neuropathy with liability to pressure palsies (HNPP)
• familial brachial plexus neuropathy
• repeated episodes of toxin exposure
• Ischemic neuropathies often have pain as a prominent feature
• Small-fiber neuropathies often present with burning pain, lightning-
like or lancinating pain, aching, or uncomfortable paresthesias
(dysesthesias).
History
• The clinical assessment should include:
• Careful past medical history
• looking for systemic diseases, eg. CTD
History
• All patients should be questioned regarding
• HIV risk factors
• diet (nutrition)
• vitamin use (especially B6)
• possibility of a tick bite (Lyme disease)
• Constitutional symtoms (malignancy)
History
Investigations:
Peripheral neuropathy
Peripheral neuropathy
Peripheral neuropathy
Peripheral neuropathy

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Peripheral neuropathy

  • 3.
  • 4.
  • 5. Loss of function “- symptoms” Disturbed function “+ symptoms” Motor nerves Wasting Hypotonia Weakness Hyporeflexia Orthopedic deformity Fasiculations Cramps The clinical response to motor nerve injury
  • 7. Loss of function “- symptoms” Disordered function “+ symptoms” Sensory “Large Fiber” ↓ Vibration ↓ Proprioception Hyporeflexia Sensory ataxia Paresthesias Sensory “Small Fiber” ↓ Pain ↓ Temperature Dysesthesias Allodynia The clinical response to sensory nerve injury
  • 8. Loss of function “- symptoms” Disturbed function “+ symptoms” Autonomic nerves ↓ Sweating Hypotension Urinary retention Impotence Vascular color changes ↑ Sweating Hypertension The clinical response to autonomic nerve injury
  • 10. The two types of peripheral neuropathies: axonopathies and myelinopathies
  • 11.
  • 12. Causes Conditions causing mononeuropathy • Acute (trauma-related) • Chronic (nerve entrapment) Disorders causing mononeuropathy multiplex Acute • Diabetes mellitus • Multifocal motor neuropathy • Vasculitic syndromes Chronic • Acquired immunodeficiency syndrome • Leprosy • Sarcoidosis
  • 13. Causes Conditions causing neuropathy with autonomic features • Alcoholism • Amyloidosis • Chemotherapy-related neuropathy • Diabetes • Heavy metal toxicity • Porphyria • Vitamin B12 deficiency
  • 14. Causes Conditions causing painful neuropathy • Diabetes • Alcoholism • Amyloidosis • Chemotherapy (heavy metal toxicity) • Idiopathic polyneuropathy • Porphyria • Paraneoplastic syndrome
  • 15. Axonal & Demyelinating causes • Axonal • Diabetes mellitus • Alcohol • Uraemia • Cirrhosis • Amyloid • Myxoedema • Acromegaly • Paraneoplastic • Drugs and toxins • Deficiency states • Hereditary • Infection • Idiopathic • Demyelinating • Chronic inflammatory demyelinating polyradiculoneuropathy • Multifocal motor neuropathy • Paraprotein-associated demyelinating neuropathy • Charcot–Marie–Tooth disease type I and type X
  • 16.
  • 17.
  • 18. In short Inherited: e.g. Charcot-Marie-Tooth disease (HMSN) Infectious: e.g. Leprosy Inflammatory: e.g. Guillain Barre syndrome (AIDP) Neoplastic: e.g. Monoclonal gammopathy Metabolic: e.g. Diabetes Drug: e.g. Vincristine Toxic: e.g. Ethanol
  • 19. History • The temporal course of a neuropathy varies, based on the etiology. • Trauma or ischemic infarction-acute, with the most severe symptoms at onset • Inflammatory and some metabolic neuropathies have a subacute course extending over days to weeks. • A chronic course over weeks to months is the hallmark of most toxic and metabolic neuropathies
  • 20. History • A chronic, slowly progressive neuropathy over many years • Hereditary neuropathies • Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) • Neuropathies with a relapsing and remitting course include • CIDP • acute porphyria • Refsum's disease • hereditary neuropathy with liability to pressure palsies (HNPP) • familial brachial plexus neuropathy • repeated episodes of toxin exposure
  • 21. • Ischemic neuropathies often have pain as a prominent feature • Small-fiber neuropathies often present with burning pain, lightning- like or lancinating pain, aching, or uncomfortable paresthesias (dysesthesias). History
  • 22. • The clinical assessment should include: • Careful past medical history • looking for systemic diseases, eg. CTD History
  • 23. • All patients should be questioned regarding • HIV risk factors • diet (nutrition) • vitamin use (especially B6) • possibility of a tick bite (Lyme disease) • Constitutional symtoms (malignancy) History