极端副神经下神经节囊肿。第1部分:原则和含义。

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Godard C W de Ruiter, Byung-Chul Son, Kirsten M Hayford, B Matthew Howe, Kimberly K Amrami, Miguel A Reina, Robert J Spinner
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引用次数: 0

摘要

目的:用统一关节理论解释神经节囊肿(INGCs)的形成和发展。其原理包括关节液通过关节分支从滑膜关节流出到母神经和囊肿,沿着阻力最小的路径,依赖于压力和压力通量。所谓的极端腓或胫骨INGCs的发生在腘窝延伸到坐骨神经已被报道。以前曾报道过一种罕见的变异,即神经外膜外的神经副膜下腔室内的环状囊肿,但其机制和形态尚未明确。在这项研究中,作者旨在研究这种类型的囊肿,以挑战统一关节理论的原则。方法:对4例新发腓神经INGCs合并坐骨神经及其远端分支“极端副神经下囊肿”患者进行分析,其中3例发生在胫腓骨上关节(STFJ), 1例发生在膝关节。另外三例已知的极端神经副膜下囊肿(2例腓骨和1例胫骨来自STFJ)和1例腓骨神经副膜下囊肿在文献中被重新解释。对临床表现、MR图像和手术结果进行分析。结果:8例患者沿坐骨神经、胫骨神经、腓总神经、腓肠神经、腓深浅神经均有不同程度的神经副下延伸,在坐骨神经分叉处,神经副下与神经副下相通(即交叉)。序贯MRI显示7例患者动态变化,包括极端上升和下降。6例在坐骨神经分叉处出现神经外破裂的副神经下囊肿,并扩散到周围组织。结论:作者提供的病理解剖和病理生理证据支持极端副神经下囊肿遵循关节理论的原则。他们提出了一种分布模式,解释了腓骨或胫骨INGCs和脑膜下囊肿患者沿坐骨神经及其远端分支的极端副神经下囊肿的发生和演变。在副神经下腔室交叉可以在连接的神经内潜在地广泛分布。此外,由于再吸收或神经外破裂,动态因素可导致囊肿大小和外观的剧烈变化。在本研究的第2部分中,作者提供的证据表明,神经外膜的开窗允许囊肿从脑膜下到神经副下、神经副下到神经副下和神经副下到脑膜下隔室。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extreme subparaneurial ganglion cysts. Part 1: Principles and implications.

Objective: The formation and propagation of intraneural ganglion cysts (INGCs) is being elucidated by the unified articular theory. Its principles include a connection for joint fluid to egress from a synovial joint via an articular branch to a parent nerve and cyst following the path of least resistance, dependent on pressures and pressure fluxes. The occurrence of so-called extreme peroneal or tibial INGCs in the popliteal fossa extending to the sciatic nerve has been reported. One rarely described variant with a circumferential cyst within the subparaneurial compartment outside the epineurium of nerve(s) has been previously illustrated, but its mechanism and morphology have not been clarified. In this study, the authors aimed to investigate this type of cyst to challenge the principles of the unified articular theory.

Methods: Four novel cases of patients with peroneal INGCs and "extreme subparaneurial cyst(s)" of the sciatic nerve and its distal branches were investigated: 3 arose from the superior tibiofibular joint (STFJ) and 1 from the knee joint. Three other cases of recognized extreme subparaneurial cyst (2 peroneal and 1 tibial from the STFJ) and 1 case of a peroneal subparaneurial cyst in the literature were reinterpreted. Data on clinical presentation, MR images, and surgical results were analyzed.

Results: In all 8 cases, subparaneurial extension was observed to different degrees along the sciatic, tibial, common peroneal, sural, and deep and superficial peroneal nerves, as was subparaneurial-to-subparaneurial communication at the sciatic nerve bifurcation (i.e., crossover). Sequential MRI performed in 7 patients showed variable dynamic changes, including extreme ascent and descent. Extraneural rupture of the subparaneurial cyst, with spread into the surrounding tissue, was present at the sciatic nerve bifurcation in 6 cases.

Conclusions: The authors provide pathoanatomical and pathophysiological evidence supporting that extreme subparaneurial cysts follow the principles of the articular theory. They propose a distribution pattern that explains the occurrence and evolution of extreme subparaneurial cysts along the sciatic nerve and its distal branches in patients with peroneal or tibial INGCs and subepineurial cysts. Crossover in the subparaneurial compartment allows potentially extensive circumferential distribution within connected nerves. Also, dynamic factors can lead to dramatic changes in cyst size and appearance from reabsorption or extraneural rupture. In Part 2 of this study, the authors provide evidence showing that a fenestration in the epineurium allows cysts to pass from the subepineurial-to-subparaneurial, subparaneurial-to-subparaneurial, and subparaneurial-to-subepimyseal compartments.

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来源期刊
Journal of neurosurgery
Journal of neurosurgery 医学-临床神经学
CiteScore
7.20
自引率
7.30%
发文量
1003
审稿时长
1 months
期刊介绍: The Journal of Neurosurgery, Journal of Neurosurgery: Spine, Journal of Neurosurgery: Pediatrics, and Neurosurgical Focus are devoted to the publication of original works relating primarily to neurosurgery, including studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology. The Editors and Editorial Boards encourage submission of clinical and laboratory studies. Other manuscripts accepted for review include technical notes on instruments or equipment that are innovative or useful to clinicians and researchers in the field of neuroscience; papers describing unusual cases; manuscripts on historical persons or events related to neurosurgery; and in Neurosurgical Focus, occasional reviews. Letters to the Editor commenting on articles recently published in the Journal of Neurosurgery, Journal of Neurosurgery: Spine, and Journal of Neurosurgery: Pediatrics are welcome.
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