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¸¸¼º ¿°Áõ¼º Å»¼öÃʼº ½Å°æº´Áõ: ´ç´¢º´ À¯¹«¿¡ µû¸¥ ÀÓ»óÀû, Àü±â»ý¸®ÇÐÀû ¼Ò°ßÀÇ ºñ±³ Chronic Inflammatory Demyelinating Poly neuropathy: Comparison of Clinical and Electrophsiological Features in Patients with and without Diabetes

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±Ç¼®¹ü ( Kwon Seok-Beom ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç

±Ç±âÇÑ ( Kwon Ki-Han ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
Á¤»ê ( Jung San ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
Á¶¼öÁø ( Cho Soo-Jin ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
¹Î¾ç±â ( Minn Yang-Ki ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
ÃÖÈÖö ( Choi Hui-Chul ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç
Ȳ¼ºÈñ ( Hwang Sung-Hee ) 
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ ½Å°æ°úÇб³½Ç

Abstract


Objectives: There is growing evidence that idiopathic chronic inflammatory demyelinating polyneuropathy
(I-CIDP) and polyneuropathy in patients with diabetes mellitus (DM) that meets the clinical and
electrophysiological criteria for CIDP (DM-CIDP) have many similarities. We performed this study to
determine whether a subset of DM-CIDP are similar to I-CIDP employing proposed clinical and electrophysiologic
criteria for CIDP.

Methods: We compared the clinical (age, sex, symptom duration, pattern, course, motor scale, sensory
scale, total clinical scale, and M-Rankin score, etc.) and electrodiagnostic (routine nerve conduction studies
including median, ulnar, peroneal, and posterior tibial nerves) features of 9 patients (M=5, F=4) with
DM-CIDP to those of 11 patients (M=4, F=7) with I-CIDP.

Results: The patients with DM-CIDP displayed clinical, electrophysiologic features that were similar to
those in patients with I-CIDP.

Conclusion: Our study showed the influences of diabetes in patients with CIDP are insignificant and
DM-CIDP is electrophysiologically indistinguishable from idiopathic CIDP. It is important to separate
immune-mediated, demyelinating polyneuropathy in diabetic patients (DM-CIDP) from axonal polyneuropathy
because the former responds to immunomodulatory treatment.

Å°¿öµå

Short segment nerve conduction study;sensitivity

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