Normal anatomy, variants and factors associated with the cervical vagus nerve topography: a high-resolution ultrasound study

Author(s):  
Eleni Drakonaki ◽  
Gregory Clouverakis ◽  
Maria Piagkou ◽  
Ioannis Koliarakis ◽  
Phaedon D. Zavras ◽  
...  
2018 ◽  
Vol 9 ◽  
Author(s):  
Johann Otto Pelz ◽  
Elena Belau ◽  
Christopher Fricke ◽  
Joseph Classen ◽  
David Weise

Author(s):  
F. Sartucci ◽  
T. Bocci ◽  
M. Santin ◽  
P. Bongioanni ◽  
G. Orlandi

Abstract Background and rationale Histopathological studies revealed degeneration of the dorsal motor nucleus of the vagus nerve (VN) early in the course of idiopathic Parkinson’s disease (IPD). Degeneration of VN axons should be detectable by high-resolution ultrasound (HRUS) as a thinning of the nerve trunk. In order to establish if the VN exhibits sonographic signs of atrophy in IPD, we examined patients with IPD compared with age-matched controls. Material and methods We measured the caliber (cross-sectional area, CSA) and perimeter of the VN in 20 outpatients with IPD (8 females and 12 males; mean age 73.0 + 8.6 years) and in age-matched controls using HRUS. Evaluation was performed by blinded raters using an Esaote MyLab Gamma device in conventional B-Mode with an 8–19 MHz probe. Results In both sides, the VN CSA was significantly smaller in IPD outpatients than in controls (right 2.37 + 0.91, left 1.87 + 1.35 mm2 versus 6.0 + 1.33, 5.6 + 1.26 mm2; p <0.001), as well as the perimeter (right 5.06 + 0.85, left 4.78 + 1.74 mm versus 8.87 + 0.86, 8.58 + 0.97 mm; p <0.001). There were no significant correlations between VN CSA and age, the Hoehn and Yahr scale, L-dopa therapy, and disease duration. Conclusion Our findings provide evidence of atrophy of the VNs in IPD patients by HRUS. Moreover, HRUS of the VN represent a non-invasive easy imaging modality of screening in IPD patients independent of disease stage and duration and an interesting possible additional index of disease.


2003 ◽  
Vol 202 (2) ◽  
pp. 239-247 ◽  
Author(s):  
Jurgen E. Schneider ◽  
Simon D. Bamforth ◽  
Cassandra R. Farthing ◽  
Kieran Clarke ◽  
Stefan Neubauer ◽  
...  

1986 ◽  
Vol 15 (7) ◽  
pp. 536-540 ◽  
Author(s):  
Paul C. Hajek ◽  
Lori L. Baker ◽  
Ann Bjorkengren ◽  
David J. Sartoris ◽  
Christian H. Neumann ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Leif A. Havton ◽  
Natalia P. Biscola ◽  
Esther Stern ◽  
Plamen V. Mihaylov ◽  
Chandrashekhar A. Kubal ◽  
...  

AbstractThe vagus nerve provides motor, sensory, and autonomic innervation of multiple organs, and electrical vagus nerve stimulation (VNS) provides an adjunctive treatment option for e.g. medication-refractory epilepsy and treatment-resistant depression. The mechanisms of action for VNS are not known, and high-resolution anatomical mapping of the human vagus nerve is needed to better understand its functional organization. Electron microscopy (EM) is required for the detection of both myelinated and unmyelinated axons, but access to well-preserved human vagus nerves for ultrastructural studies is sparse. Intact human vagus nerve samples were procured intra-operatively from deceased organ donors, and tissues were immediately immersion fixed and processed for EM. Ultrastructural studies of cervical and sub-diaphragmatic vagus nerve segments showed excellent preservation of the lamellated wall of myelin sheaths, and the axolemma of myelinated and unmyelinated fibers were intact. Microtubules, neurofilaments, and mitochondria were readily identified in the axoplasm, and the ultrastructural integrity of Schwann cell nuclei, Remak bundles, and basal lamina was also well preserved. Digital segmentation of myelinated and unmyelinated axons allowed for determination of fiber size and myelination. We propose a novel source of human vagus nerve tissues for detailed ultrastructural studies and mapping to support efforts to refine neuromodulation strategies, including VNS.


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