肘部正中神经节内囊肿:关节连接的首个已知病例及对过去的反思。说明性病例。

Andres A Maldonado, Kimberly K Amrami, Christoph Hirche, Robert J Spinner
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引用次数: 0

摘要

背景:除了肘部正中神经外,神经节内囊肿的关节起源以前已有描述,并得到了很好的支持:作者介绍了一名肘部正中神经节内囊肿患者,磁共振成像(MRI)显示该囊肿与桡侧近端关节相连。一名 63 岁的男子出现拇指屈曲无力以及拇指、食指和中指疼痛。肌电图证实肘部正中神经有病变。核磁共振成像显示,正中神经硬膜内囊肿和硬膜外囊肿均来自桡侧近端关节。术前通过核磁共振成像和术中使用吲哚青绿鉴定了囊肿和桡侧近端关节之间的关节支。在断开关节支和椎弓根,并对硬膜内外囊肿进行减压后,患者在 6 个月后恢复了 M4 级运动功能,神经性疼痛也在术后立即缓解:作者介绍了首例与桡侧近端关节相连的正中硬膜内囊肿病例。作者认为,该报告和其他历史数据加强了神经节内囊肿的关节理论,不仅在该部位,而且在所有部位都是如此。https://thejns.org/doi/10.3171/CASE24564。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Median intraneural ganglion cyst at the elbow: the first known example of a joint connection and a reflection on the past. Illustrative case.

Background: The articular origin of intraneural ganglion cysts has been previously described and well supported, except for the median nerve at the level of the elbow.

Observations: The authors present a patient with a median intraneural ganglion cyst at the elbow region and magnetic resonance imaging (MRI) evidence of a joint connection to the proximal radioulnar joint. A 63-year-old man presented with thumb flexion weakness and dysesthesias in the thumb, index, and middle fingers. Electromyography confirmed a median nerve lesion at the elbow. MRI demonstrated a median intraneural cyst as well as an extraneural cyst, both arising from the proximal radioulnar joint. The articular branch between the cyst and the proximal radioulnar joint was identified preoperatively on MRI and intraoperatively using indocyanine green. Following disconnection of the articular branch and pedicle and decompression of the intra- and extraneural cysts, the patient recovered grade M4 motor function after 6 months, with resolution of neuropathic pain immediately after surgery.

Lessons: The authors present the first case of a median intraneural cyst with a joint connection to the proximal radioulnar joint. The authors believe that this report along with other historical data strengthens the articular theory for intraneural ganglion cysts not only at this site but at all sites. https://thejns.org/doi/10.3171/CASE24564.

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