Contrast-free Ultrasound Microvascular Imaging for Intraoperative Detection of Human Spinal Cord Tumor: An In vivo Feasibility Study

Author(s):  
Lijie Huang ◽  
Yayu Hao ◽  
Linkai Jing ◽  
Yuanyuan Wang ◽  
Qiong He ◽  
...  
NeuroImage ◽  
2013 ◽  
Vol 82 ◽  
pp. 416-425 ◽  
Author(s):  
Novena A. Rangwala ◽  
David B. Hackney ◽  
Weiying Dai ◽  
David C. Alsop

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 573 ◽  
Author(s):  
So-Jung Gwak ◽  
Jeoung Soo Lee

Spinal cord tumors (SCT) are uncommon neoplasms characterized by irregular growth of tissue inside the spinal cord that can result in non-mechanical back pain. Current treatments for SCT include surgery, radiation therapy, and chemotherapy, but these conventional therapies have many limitations. Suicide gene therapy using plasmid encoding herpes simplex virus-thymidine kinase (pHSV-TK) and ganciclovir (GCV) has been an alternative approach to overcome the limitations of current therapies. However, there is a need to develop a carrier that can deliver both pHSV-TK and GCV for improving therapeutic efficacy. Our group developed a cationic, amphiphilic copolymer, poly (lactide-co-glycolide) -graft-polyethylenimine (PgP), and demonstrated its efficacy as a drug and gene carrier in both cell culture studies and animal models. In this study, we evaluated PgP as a gene carrier and demonstrate that PgP can efficiently deliver reporter genes, pGFP in rat glioma (C6) cells in vitro, and pβ-gal in a rat T5 SCT model in vivo. We also show that PgP/pHSV-TK with GCV treatment showed significantly higher anticancer activity in C6 cells compared to PgP/pHSV-TK without GCV treatment. Finally, we demonstrate that PgP/pHSV-TK with GCV treatment increases the suicide effect and apoptosis of tumor cells and reduces tumor size in a rat T5 SCT model.


2021 ◽  
pp. 1-10
Author(s):  
Amro Al-Habib ◽  
Wajda Alhothali ◽  
Abdulrahman Albakr ◽  
Sherif Elwatidy ◽  
Ghaida Alawaji ◽  
...  

OBJECTIVE Although evaluating tissue elasticity has various clinical applications, spinal cord elasticity (SCE) in humans has never been well documented. In this study, the authors aimed to evaluate the impact of compression on human SCE in vivo. METHODS The authors prospectively assessed SCE using intraoperative shear wave elastography (SWE). All consecutive patients undergoing spinal cord (SC) decompression (laminectomy or corpectomy) between June 2018 and June 2019 were included. After intraoperative exposure of the patient’s dura mater, at least three SWE measurements of the SC and its coverings were performed. Intraoperative neurological monitoring in the form of motor and somatosensory evoked potentials was utilized. Cases were divided into two groups based on the state of SC compression following bone removal (laminectomy or corpectomy): patients with adequate decompression (the decompressed SC group [DCG]) following bone removal and patients with remining compression, e.g., compressing tumor or instability (the compressed SC group [COG]). RESULTS A total of 25 patients were included (8 females and 17 males) with a mean age of 48.28 ± 21.47 years. Most cases were degenerative diseases (10 cases) followed by tumors (6 cases), and the compression was observed at cervical (n = 14), thoracic (n = 9), and conus medullaris (n = 2) levels. The COG (6 cases) expressed significantly higher elasticity values, i.e., greater stiffness (median 93.84, IQR 75.27–121.75 kPa) than the decompressed SC in DCG (median 9.35, IQR 6.95–11.22 kPa, p < 0.001). Similarly, the compressed dura mater in the COG was significantly stiffer (mean ± SD 121.83 ± 70.63 kPa) than that in the DCG (29.78 ± 18.31 kPa, p = 0.042). Following SC decompression in COG, SCE values were significantly reduced (p = 0.006; adjusted for multiple comparisons). Intraoperative monitoring demonstrated no worsening from the baseline. CONCLUSIONS The current study is to the authors’ knowledge the first to quantitatively demonstrate increased stiffness (i.e., elasticity value) of the human SC and dura mater in response to external compression in vivo. It appears that SCE is a dynamic phenomenon and is reduced following decompression. Moreover, the evaluation of human SCE using the SWE technique is feasible and safe. Information from future studies aiming to further define SCE could be valuable in the early and accurate diagnosis of the compressed SC.


2010 ◽  
Vol 16 (4) ◽  
pp. 406-411 ◽  
Author(s):  
Emma C Tallantyre ◽  
Lars Bø ◽  
Omar Al-Rawashdeh ◽  
Trudy Owens ◽  
Chris H Polman ◽  
...  

Growing evidence suggests that axonal degeneration rather than demyelination is the pathological substrate underlying chronic, irreversible disability in multiple sclerosis. However, direct evidence linking clinical disability measured in vivo with corresponding post-mortem measures of axonal pathology is lacking. Our objective in this study was to investigate the relationship between motor disability accumulated by patients with multiple sclerosis during life and the degree of axonal loss observed in their descending motor tracts after death. Human spinal cord derived at autopsy from 45 patients with multiple sclerosis was investigated. The medical records of each patient were reviewed by a multiple sclerosis neurologist to determine the degree of motor disability reached before death. Spinal cord sections were stained immunohistochemically. The degree of demyelination and the number of surviving corticospinal tract axons were measured in each patient. Patients who had accumulated higher levels of motor disability prior to death demonstrated fewer surviving corticospinal axons. Motor disability did not correlate with degree of demyelination. This study provides for the first time, direct clinico-pathological evidence that axonal loss is the pathological substrate of established disability in multiple sclerosis.


NeuroImage ◽  
2015 ◽  
Vol 118 ◽  
pp. 494-507 ◽  
Author(s):  
Tanguy Duval ◽  
Jennifer A. McNab ◽  
Kawin Setsompop ◽  
Thomas Witzel ◽  
Torben Schneider ◽  
...  

Spine ◽  
2014 ◽  
Vol 39 (4) ◽  
pp. E262-E269 ◽  
Author(s):  
Léo Fradet ◽  
Pierre-Jean Arnoux ◽  
Jean-Philippe Ranjeva ◽  
Yvan Petit ◽  
Virginie Callot

2013 ◽  
Vol 27 (3) ◽  
pp. 257-267 ◽  
Author(s):  
Manuel Taso ◽  
Arnaud Le Troter ◽  
Michaël Sdika ◽  
Jean-Philippe Ranjeva ◽  
Maxime Guye ◽  
...  

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