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[继发于正中神经罕见解剖变异的腕管综合征]

[Carpal tunnel syndrome secondary to a rare anatomical variation of the median nerve].

作者信息

Tahir Amine, Sdoudi Amine, Chahed Mohamed, Elbaitil Aniss, Fakherdine Lkoutbi, Sbihi Yasser, Bennouna Driss, Fadili Mustafa

机构信息

Traumatologie-Orthopédie Aile 4, CHU Ibn Rochd, Casablanca, Maroc.

出版信息

Pan Afr Med J. 2018 Sep 20;31:39. doi: 10.11604/pamj.2018.31.39.15526. eCollection 2018.

DOI:10.11604/pamj.2018.31.39.15526
PMID:30918565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6430855/
Abstract

Carpal tunnel syndrome is one of the the most common reasons for consultation in hand surgery with an annual incidence of 300 per 100 000 inhabitants and, in France, of 80 000 surgical interventions. In most cases, carpal tunnel syndrome is idiopathic occurring without a recognizable cause. However, beyond these forms, the merging of several mechanisms can explain the cause-and-effect relationship of this pathology . This study aimed to highlight an exceptional association of a carpal tunnel syndrome secondary to a rare anatomical variety of the median nerve.

摘要

腕管综合征是手部外科门诊最常见的病因之一,年发病率为每10万居民中有300例,在法国,每年有80000例手术治疗。在大多数情况下,腕管综合征是特发性的,没有可识别的病因。然而,除了这些类型外,多种机制的合并可以解释这种病理的因果关系。本研究旨在强调一种罕见的正中神经解剖变异继发腕管综合征的特殊关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/12f30ad5adff/PAMJ-31-39-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/eb8aecffacc6/PAMJ-31-39-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/8a8bf1d7b5ce/PAMJ-31-39-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/3eaa27c37de4/PAMJ-31-39-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/12f30ad5adff/PAMJ-31-39-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/eb8aecffacc6/PAMJ-31-39-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/8a8bf1d7b5ce/PAMJ-31-39-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/3eaa27c37de4/PAMJ-31-39-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd6b/6430855/12f30ad5adff/PAMJ-31-39-g004.jpg

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Pan Afr Med J. 2018 Sep 20;31:39. doi: 10.11604/pamj.2018.31.39.15526. eCollection 2018.
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