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A  CASE  OF  FLACCID QUADRIPARESIS S.GEETHALAKSHMI PROF  DR.MAGESHKUMAR’S  UNIT
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On  Examination ,[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]
CNS ,[object Object],[object Object],[object Object],RIGHT LEFT BULK EQUAL  ON BOTH  SIDES POWER UL-  3 UL  - 3 LL -  3 LL  - 3 TONE DEEP TENDON REFLEX ---- ---- PLANTAR REFLEX No response No response
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PROVISIONAL DIAGNOSIS ,[object Object]
DD: ,[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]
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],LFT BILIRUBIBIN TOT 0.9mg ALKALINE  90 U PHOSPHATASE AST  11 U ALT  23 U TOT PROTEINS 6.3g  SR.ALBUMIN  4.4g  Sr.CALCIUM  8.8 mg Sr.PHOSPHORUS  4 mg VDRL – NR
NEURO MEDICINE OPINION ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Cont…d ,[object Object],[object Object],[object Object],[object Object]
MEANWHILE…… ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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NERVE CONDUCTION STUDIES SECOND EPISODE THIRD EPISODE UPPER LIMB SNAPS – NORMAL AMPLITUDE PRESERVED F WAVE ABSENT IN LT ULNAR, MEDIAN & RT ULNAR NERVES SNAPS – NORMAL CMAP & F WAVE, LT ULNAR LATENCY PROLONGED Conduction blocks+  LOWER LIMB SNAPS – NORMAL VELOCITY  F WAVE ABSENT  IN ALL NERVES SNAPS –NORMAL CMAP –LATENCY PROLONGED F WAVE NOT OBTAINED AMPLITUDE DECREASED Conduction blocks+
Similarity &Differences Btn the 3 episodes ,[object Object],[object Object],[object Object],[object Object]
SINCE IT WAS RECURRENT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
FURTHER COURSE ,[object Object],[object Object],[object Object],[object Object]
PROBABLE  DIAGNOSIS ,[object Object],[object Object],[object Object],[object Object],[object Object],CIDP
INTRODUCTION:  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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PATHOGENESIS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],DEMYELINATION.  -macrophages mediated.  multifocal.esp with active demyelination. - segmental. -thin myelin sheath. ONION bulb formation.
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AAN CRITERIA ,[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]
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NERVE BIOPSY- ITS ROLE  The diagnostic utility of nerve biopsy for suspected CIDP is controversial . Nerve biopsy is used mainly when other studies fail to clearly establish the diagnosis of CIDP, particularly when electrophysiologic criteria for demyelination are not met. #A major limitation of nerve biopsy is suboptimal sensitivity and specificity #CIDP is a multifocal disorder, and motor nerve fibers tend to be more affected than sensory nerves (the usual nerves used for biopsy). As a result, the biopsy sample may not demonstrate the demyelination. In addition, the inflammatory component of CIDP may not be prominent and thus may not be apparent on biopsy.
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WHY NERVE BIOPSY NOT DONE IN OUR CASE ,[object Object],[object Object]
DIAGNOSTIC CRITERIA FOR CIDP ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
KOSKI CRITERIA  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TREATMENT OPTIONS:  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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RECURRENT AIDP & CIDP CONTINUM OR DISTINCT ENTITIES?? ,[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]
SLE  IN  CIDP ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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Nervous system n SLE
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THANK  U
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CIDP ,[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]
 

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A Case of CIDP

  • 1. A CASE OF FLACCID QUADRIPARESIS S.GEETHALAKSHMI PROF DR.MAGESHKUMAR’S UNIT
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  • 15. NERVE CONDUCTION STUDIES SECOND EPISODE THIRD EPISODE UPPER LIMB SNAPS – NORMAL AMPLITUDE PRESERVED F WAVE ABSENT IN LT ULNAR, MEDIAN & RT ULNAR NERVES SNAPS – NORMAL CMAP & F WAVE, LT ULNAR LATENCY PROLONGED Conduction blocks+ LOWER LIMB SNAPS – NORMAL VELOCITY F WAVE ABSENT IN ALL NERVES SNAPS –NORMAL CMAP –LATENCY PROLONGED F WAVE NOT OBTAINED AMPLITUDE DECREASED Conduction blocks+
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  • 29. NERVE BIOPSY- ITS ROLE The diagnostic utility of nerve biopsy for suspected CIDP is controversial . Nerve biopsy is used mainly when other studies fail to clearly establish the diagnosis of CIDP, particularly when electrophysiologic criteria for demyelination are not met. #A major limitation of nerve biopsy is suboptimal sensitivity and specificity #CIDP is a multifocal disorder, and motor nerve fibers tend to be more affected than sensory nerves (the usual nerves used for biopsy). As a result, the biopsy sample may not demonstrate the demyelination. In addition, the inflammatory component of CIDP may not be prominent and thus may not be apparent on biopsy.
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