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Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies

BACKGROUND: Multifocal motor neuropathy (MMN), Lewis-Sumner syndrome (LSS), and many chronic inflammatory demyelinating polyradiculoneuropathies (CIDPs) are representative of acquired multifocal polyneuropathy and are characterized by conduction block (CB). This retrospective study aimed to investig...

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Autores principales: Zhou, Xia-Jun, Zhu, Ying, Zhu, De-Sheng, Han, Lu, Liu, Qian-Yun, Liang, Xiao-Niu, Hao, Yong, Li, Ze-Zhi, Guan, Yang-Tai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722580/
https://www.ncbi.nlm.nih.gov/pubmed/32947359
http://dx.doi.org/10.1097/CM9.0000000000001073
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author Zhou, Xia-Jun
Zhu, Ying
Zhu, De-Sheng
Han, Lu
Liu, Qian-Yun
Liang, Xiao-Niu
Hao, Yong
Li, Ze-Zhi
Guan, Yang-Tai
author_facet Zhou, Xia-Jun
Zhu, Ying
Zhu, De-Sheng
Han, Lu
Liu, Qian-Yun
Liang, Xiao-Niu
Hao, Yong
Li, Ze-Zhi
Guan, Yang-Tai
author_sort Zhou, Xia-Jun
collection PubMed
description BACKGROUND: Multifocal motor neuropathy (MMN), Lewis-Sumner syndrome (LSS), and many chronic inflammatory demyelinating polyradiculoneuropathies (CIDPs) are representative of acquired multifocal polyneuropathy and are characterized by conduction block (CB). This retrospective study aimed to investigate the demyelinating distribution and the selective vulnerability of MMN, LSS, and CIDP with CB (CIDP-CB) in nerves. METHODS: Fifteen LSS subjects (107 nerves), 24 MMN subjects (176 nerves), and 17 CIDP-CB subjects (110 nerves) were included. Their clinical information was recorded, blood and cerebrospinal fluid tests were conducted, and nerve conductions of the median, ulnar, radial, peroneal, and tibial nerves were evaluated. CB, temporal dispersion, distal motor latency (DML), and F-wave latency were recorded, and nerve conduction velocity, terminal latency index, and modified F-wave ratio were calculated. RESULTS: CB was more likely to occur around the elbow in CIDP-CB than in MMN (78.6% vs. 6.8%, P < 0.01) but less likely to occur between the wrist and the elbow than in LSS (10.7% vs. 39.3%, P < 0.05). Tibial nerve CB was most frequently observed in MMN (47.4%, P < 0.05). CIDP-CB was characterized by a prolonged DML in all nerves, and slow motor nerve velocity of the upper limb was significant when CB nerves were excluded (P < 0.05). CONCLUSIONS: We report the different distributions of segmental and diffuse demyelination of the ulnar and tibial nerves in LSS, MMN, and CIDP-CB. These distinct distributions could help in differentiating among these conditions.
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spelling pubmed-77225802020-12-08 Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies Zhou, Xia-Jun Zhu, Ying Zhu, De-Sheng Han, Lu Liu, Qian-Yun Liang, Xiao-Niu Hao, Yong Li, Ze-Zhi Guan, Yang-Tai Chin Med J (Engl) Original Articles BACKGROUND: Multifocal motor neuropathy (MMN), Lewis-Sumner syndrome (LSS), and many chronic inflammatory demyelinating polyradiculoneuropathies (CIDPs) are representative of acquired multifocal polyneuropathy and are characterized by conduction block (CB). This retrospective study aimed to investigate the demyelinating distribution and the selective vulnerability of MMN, LSS, and CIDP with CB (CIDP-CB) in nerves. METHODS: Fifteen LSS subjects (107 nerves), 24 MMN subjects (176 nerves), and 17 CIDP-CB subjects (110 nerves) were included. Their clinical information was recorded, blood and cerebrospinal fluid tests were conducted, and nerve conductions of the median, ulnar, radial, peroneal, and tibial nerves were evaluated. CB, temporal dispersion, distal motor latency (DML), and F-wave latency were recorded, and nerve conduction velocity, terminal latency index, and modified F-wave ratio were calculated. RESULTS: CB was more likely to occur around the elbow in CIDP-CB than in MMN (78.6% vs. 6.8%, P < 0.01) but less likely to occur between the wrist and the elbow than in LSS (10.7% vs. 39.3%, P < 0.05). Tibial nerve CB was most frequently observed in MMN (47.4%, P < 0.05). CIDP-CB was characterized by a prolonged DML in all nerves, and slow motor nerve velocity of the upper limb was significant when CB nerves were excluded (P < 0.05). CONCLUSIONS: We report the different distributions of segmental and diffuse demyelination of the ulnar and tibial nerves in LSS, MMN, and CIDP-CB. These distinct distributions could help in differentiating among these conditions. Lippincott Williams & Wilkins 2020-11-05 2020-09-17 /pmc/articles/PMC7722580/ /pubmed/32947359 http://dx.doi.org/10.1097/CM9.0000000000001073 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Articles
Zhou, Xia-Jun
Zhu, Ying
Zhu, De-Sheng
Han, Lu
Liu, Qian-Yun
Liang, Xiao-Niu
Hao, Yong
Li, Ze-Zhi
Guan, Yang-Tai
Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title_full Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title_fullStr Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title_full_unstemmed Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title_short Different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
title_sort different distributions of nerve demyelination in chronic acquired multifocal polyneuropathies
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722580/
https://www.ncbi.nlm.nih.gov/pubmed/32947359
http://dx.doi.org/10.1097/CM9.0000000000001073
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