Literature DB >> 28472865

Electrophysiologic features of POEMS syndrome compared with MGUS-related neuropathy.

Hyunjin Kim1, Young-Min Lim1, Joo Yea Jin1, Dok Hyun Yoon2, Cheolwon Suh2, Sun-Young Kim3, Jae-Cheol Jo4, Kwang-Kuk Kim1.   

Abstract

INTRODUCTION: Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome and monoclonal gammopathy of undetermined significance (MGUS) are paraproteinemic disorders that can cause demyelinating polyneuropathy. Herein we assessed the findings of nerve conduction studies (NCS) in patients with POEMS syndrome and MGUS-related neuropathy to determine whether the NCS characteristics can help differentiate between these conditions.
METHODS: We enrolled 24 POEMS and 37 MGUS-related neuropathy patients. NCS parameters, including compound muscle action potential (CMAP), motor conduction velocity (MCV), and terminal latency index (TLI), were evaluated.
RESULTS: Compared with MGUS-related neuropathy patients, POEMS syndrome patients demonstrated a greater reduction in both the upper and lower limb CMAPs and a greater reduction in the median and ulnar MCVs. The TLIs were significantly higher in POEMS patients. DISCUSSION: NCS can help distinguish POEMS syndrome from MGUS-related neuropathy. Reduced CMAPs, slow MCVs, and high TLIs are indicative of POEMS syndrome rather than MGUS-related neuropathy. Muscle Nerve 56: E73-E77, 2017.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  MGUS-related neuropathy; POEMS syndrome; axonal loss; demyelination; nerve conduction study

Mesh:

Year:  2017        PMID: 28472865     DOI: 10.1002/mus.25684

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  1 in total

1.  Temporal dispersion in demyelination of POEMS syndrome and Castleman disease.

Authors:  Yue Hui Lau; Hazfadzila Mohd Unit; Lay Peng Lee; Weng Khean Loh; Fu Liong Hiew
Journal:  Clin Neurophysiol Pract       Date:  2020-05-31
  1 in total

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