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APPROACH TO PERIPHERAL NEUROPATHY PROF.RUCKMANI REDDY’S UNIT M1
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
What forms peripheral nerve?
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Role of nerve fibres in peripheralneuropathy
HISTORY ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Sensory symptoms ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Motor symptoms SPASMS DIIFFICULTY WITH FOOD INTAKE TREMOR WASTING OF MUSCLE MYOKYMIA DECREASED MANUAL DEXTERITY FASCICULATIONS WEAKNESS MUSCLE CRAMPS
Autonomic symptoms ANOREXIA,NAUSEA,VOMITING-GASTROPARESIS BLADDER,BOWEL,SEXUAL DYSFUNCTION HEAT INTOLERANCE SWEATING-INCREASED/DECREASED FAINTING SPELLS ORTHOSTATIC LIGHT HEADEDNESS
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
GE-SKIN,HAIR,NAILS BULLOUS LESIONS VARIEGATE PORPHYRIA HYPERPIGMENTATION OSTEOSCLEROTIC MYELOMA-POEMS SKIN HYPERPIGMENTATION LEPROSY ANGIOKERATOMAS FABRY’S DISEASE PURPURA CRYOGLOBULINEMIA PURPURA,LIVEDORETICULARIS VASCULITIS
CURLED HAIR GIANT AXONAL NEURPATHY ALOPECIA THALLIUM POISONING MEE’S LINES ARSENIC/THALLIUM INTOXICATION ICTHYOSIS REFSUM’S DISEASE
NERVE THICKENING in NPthy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
DEFORMITY in NPthy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Cranial nerves ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pattern of sensory loss Sensory loss of trunk,scalp,face d/t simultaneous damage of proximal&distal part of sensory nerve SENSORY GANGLIONOPATHY ESCUTCHEON pattern of sensory loss over abdomen and thorax SEVERE AXONAL NEUROPATHY Symmetrical,distal,legs>arms Can even progress to face  POLY NEUROPATHY
NERVE FIBRE AFFECTED? Poor balance Diminished or absent reflexes tingling Decreased joint position sense Pin & needle sensation Decreased vibration sense numbness SIGNS SYMPTOMS LARGE FIBRE NEUROPATHY
Causes of large fibre/ataxic NP ,[object Object],[object Object],[object Object],[object Object],[object Object]
SMALL FIBRE NEUROPATHY Diminished temperature sensation Tight band like pressure Insensitive to heat and cold Decreased pinprick sensation PAIN-burning,shock like,stabbing,prickling,shooting,lancinating Allodynia
Causes of small fibre neuropathy (painful NP&dissociated sensory loss) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
SMALL & LARGE FIBRE NEUROPATHY ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Motor predominant neuropathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Autonomic  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Distribution of neuropathy ,[object Object],[object Object],[object Object],[object Object],neoplasms Vascular lesions entrapment compression Direct trauma
?MONONEUROPATHY MULTIPEX ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
?POLYNEUROPATHY ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
CAUSES ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
DDs of distal symmetricNP ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
?polyneuritis cranialis ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
ANATOMIC PATTERN?
Proprioceptive weakness Distal & proximal weakness Distal weakness Vibration&proprioception>pain&temp Vibration&proprioception>pain&temp Pain&temp affected>vib,proprioception ataxia,paraesthesia Paraesthesia&weakness Dysesthesia&distal weakness rapid Acute/subacute Slow evolution Non length dependent UE,LE,face Proximal=distal Distal>proximal Length dependent NEURONAL DEMYELINATING AXONAL
Poor recovery Rapid recovery Slow recovery Axonal degeneration,no regeneration Demyelination&remyelination Axonal degeneration&regeneration Sensoryamplitudeaffected. radial>sural Velocity>amplitude Amplitude affected>velocity areflexia areflexia Distal areflexia NEURONAL DEMYELINATING AXONAL
Diabetes mellitus Diabetes mellitus MMN CMT pyridoxine CIDP HIV cisplatin diphtheria metabolic Sjogren’s GBS Toxic NEURONAL DEMYELINATING AXONAL
COURSE OF DISEASE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],ACQUIRED GENETIC Metachromaticleucodystrophy amyloidosis Tangier’s disease paraproteinemia A beta lipoproteinemia myeloma Refsum’s disease carcinoma Portugeseamyloidosis/ andrade’s disease uremia Hereditary sensory NP Diabetes mellitus Dejerine sottas disease leprosy Peronealmuscle atrophy/CMT
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HOW TO DISTINGUISH VARIOUS LMN LESIONS?
Nl/dec normal absent dec/Nl DTR + absent Usually+ absent Sensoryloss absent Usually neg Can occur severe wasting absent absent Maybe+ve marked fasciculation Prox except SMA Extraoccular,bulbar distal distal Distribution of weakness ----- More in evening ------ ----- Fatigue,diurnalweakness variation Myopathy NMJ Neuropathy AHC
INVESTIGATIONS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
NERVE BIOPSY-indications sural,sup peroneal&sup radialN METACHROMATIC LEUKODYSTROPY Paraprotein neuropathy KRABBE’S CIDPolyradiculoneuropathy LEPROSY CMT 1&3 SARCOIDOSIS Infantile neuroaxonal dystrophy AMYLOIDOSIS GIANT AXONAL NPthy VASCULITIS
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
H/O & EXAMINATION Mononeuropathy EDx Axonal/demyeln? Any systemic disorder Entrapment/compression
MNPthy multiplex axonal Demyeln +focal condcn block Vasculitis/multifocal Nerve biopsy CIDP Paraprotein,HIV,lyme
polyNPthy axonal Sub a/c c/c Toxins/systemic disease family h/o,genetics
demyelination Uniform slowing,C/C Nonuniform slowing,condnblock paraprotein Family h/o,genetics c/c or suba/c-CIDP a/c-GBS
[object Object]

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Approach to Peripheral Neuropathy

  • 1. APPROACH TO PERIPHERAL NEUROPATHY PROF.RUCKMANI REDDY’S UNIT M1
  • 2.
  • 4.
  • 5. Role of nerve fibres in peripheralneuropathy
  • 6.
  • 7.
  • 8.
  • 9. Motor symptoms SPASMS DIIFFICULTY WITH FOOD INTAKE TREMOR WASTING OF MUSCLE MYOKYMIA DECREASED MANUAL DEXTERITY FASCICULATIONS WEAKNESS MUSCLE CRAMPS
  • 10. Autonomic symptoms ANOREXIA,NAUSEA,VOMITING-GASTROPARESIS BLADDER,BOWEL,SEXUAL DYSFUNCTION HEAT INTOLERANCE SWEATING-INCREASED/DECREASED FAINTING SPELLS ORTHOSTATIC LIGHT HEADEDNESS
  • 11.
  • 12. GE-SKIN,HAIR,NAILS BULLOUS LESIONS VARIEGATE PORPHYRIA HYPERPIGMENTATION OSTEOSCLEROTIC MYELOMA-POEMS SKIN HYPERPIGMENTATION LEPROSY ANGIOKERATOMAS FABRY’S DISEASE PURPURA CRYOGLOBULINEMIA PURPURA,LIVEDORETICULARIS VASCULITIS
  • 13. CURLED HAIR GIANT AXONAL NEURPATHY ALOPECIA THALLIUM POISONING MEE’S LINES ARSENIC/THALLIUM INTOXICATION ICTHYOSIS REFSUM’S DISEASE
  • 14.
  • 15.
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  • 17.
  • 18.
  • 19. Pattern of sensory loss Sensory loss of trunk,scalp,face d/t simultaneous damage of proximal&distal part of sensory nerve SENSORY GANGLIONOPATHY ESCUTCHEON pattern of sensory loss over abdomen and thorax SEVERE AXONAL NEUROPATHY Symmetrical,distal,legs>arms Can even progress to face POLY NEUROPATHY
  • 20. NERVE FIBRE AFFECTED? Poor balance Diminished or absent reflexes tingling Decreased joint position sense Pin & needle sensation Decreased vibration sense numbness SIGNS SYMPTOMS LARGE FIBRE NEUROPATHY
  • 21.
  • 22. SMALL FIBRE NEUROPATHY Diminished temperature sensation Tight band like pressure Insensitive to heat and cold Decreased pinprick sensation PAIN-burning,shock like,stabbing,prickling,shooting,lancinating Allodynia
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 37. Proprioceptive weakness Distal & proximal weakness Distal weakness Vibration&proprioception>pain&temp Vibration&proprioception>pain&temp Pain&temp affected>vib,proprioception ataxia,paraesthesia Paraesthesia&weakness Dysesthesia&distal weakness rapid Acute/subacute Slow evolution Non length dependent UE,LE,face Proximal=distal Distal>proximal Length dependent NEURONAL DEMYELINATING AXONAL
  • 38. Poor recovery Rapid recovery Slow recovery Axonal degeneration,no regeneration Demyelination&remyelination Axonal degeneration&regeneration Sensoryamplitudeaffected. radial>sural Velocity>amplitude Amplitude affected>velocity areflexia areflexia Distal areflexia NEURONAL DEMYELINATING AXONAL
  • 39. Diabetes mellitus Diabetes mellitus MMN CMT pyridoxine CIDP HIV cisplatin diphtheria metabolic Sjogren’s GBS Toxic NEURONAL DEMYELINATING AXONAL
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45. HOW TO DISTINGUISH VARIOUS LMN LESIONS?
  • 46. Nl/dec normal absent dec/Nl DTR + absent Usually+ absent Sensoryloss absent Usually neg Can occur severe wasting absent absent Maybe+ve marked fasciculation Prox except SMA Extraoccular,bulbar distal distal Distribution of weakness ----- More in evening ------ ----- Fatigue,diurnalweakness variation Myopathy NMJ Neuropathy AHC
  • 47.
  • 48.
  • 49.
  • 50. NERVE BIOPSY-indications sural,sup peroneal&sup radialN METACHROMATIC LEUKODYSTROPY Paraprotein neuropathy KRABBE’S CIDPolyradiculoneuropathy LEPROSY CMT 1&3 SARCOIDOSIS Infantile neuroaxonal dystrophy AMYLOIDOSIS GIANT AXONAL NPthy VASCULITIS
  • 51.
  • 52. H/O & EXAMINATION Mononeuropathy EDx Axonal/demyeln? Any systemic disorder Entrapment/compression
  • 53. MNPthy multiplex axonal Demyeln +focal condcn block Vasculitis/multifocal Nerve biopsy CIDP Paraprotein,HIV,lyme
  • 54. polyNPthy axonal Sub a/c c/c Toxins/systemic disease family h/o,genetics
  • 55. demyelination Uniform slowing,C/C Nonuniform slowing,condnblock paraprotein Family h/o,genetics c/c or suba/c-CIDP a/c-GBS
  • 56.