Journal of neurosurgery. Spine
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In the present study, the authors identified the etiology, precipitating factors, and outcomes of perioperative brachial plexus injuries following spine surgery. ⋯ Brachial plexus injuries are an increasingly recognized complication following spinal surgery. Proper attention to patient positioning with the use of intraoperative electrophysiological monitoring techniques could minimize injury.
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Review
Outcome after microsurgery in 14 patients with spinal cavernomas and review of the literature.
Spinal cavernomas are rare, but can cause significant neurological deficits due to mass effect and extralesional hemorrhage. The authors present their results of microsurgical treatment of 14 consecutive patients with spinal cavernoma, and review the literature. ⋯ Microsurgical removal of spinal cavernomas alleviates sensorimotor deficits and pain caused by mass effect and hemorrhage. However, bladder dysfunction remains unchanged after surgery.
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Case Reports
Paraspinal-approach transforaminal lumbar interbody fusion for the treatment of lumbar foraminal stenosis.
Foraminal stenosis is a common cause of lumbar radicular symptoms. Recognition of the dynamic pathology, as well as the static anatomical changes, is important to achieving successful surgical outcomes. Excessive facet and anulus removal leads to subsequent disc space narrowing and/or segmental instability, which can cause poor results after decompressive surgery. The objective of this study was to evaluate the efficacy of the paraspinal-approach transforaminal lumbar interbody fusion (TLIF) in the treatment of lumbar foraminal stenosis. ⋯ The paraspinal-approach TLIF is a minimally invasive, safe, and secure procedure for treating lumbar foraminal lesions. Direct visualization and decompression for the foraminal lesion, distraction of the collapsed disc space, and stabilization of the unstable segments can be achieved simultaneously through the paraspinal approach, which produces successful clinical and radiological results.
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Thoracic pedicle screw instrumentation is often indicated in the treatment of trauma, deformity, degenerative disease, and oncological processes. Although classic teaching for cervical spine constructs is to bridge the cervicothoracic junction (CTJ) when instrumenting in the lower cervical region, the indications for extending thoracic constructs into the cervical spine remain unclear. The goal of this study was to determine the role of ligamentous and facet capsule (FC) structures at the CTJ as they relate to stability above thoracic pedicle screw constructs. ⋯ When stopping thoracic constructs at T-1, care should be taken to preserve the SSL/ISL complex to avoid destabilization of the supra-adjacent CTJ, which may manifest clinically as proximal-junction kyphosis. In an analogous fashion, if a T-1 laminectomy is required for neural decompression or surgical access, consideration should be given to extending instrumentation into the cervical spine. Facet capsule disruption, as might be encountered during T-1 pedicle screw placement, may not be an acutely destabilizing event, due to the interaction of the C7–T1 facet joints with T-1 instrumentation.
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Granulocyte colony-stimulating factor (G-CSF) is a hematopoietic cytokine that induces undifferentiated stem cells from the bone marrow (BM) into the peripheral blood. Stem cell factor (SCF) is also a hematopoietic cytokine that stimulates the differentiation and proliferation of neural stem cells and has neuroprotective effects. In cerebrally infarcted mice, the combination of G-CSF and SCF promotes the differentiation of BM-derived cells into neural cells, stimulates the proliferation of intrinsic neural stem cells, and improves motor function. The object of this study was to investigate the effects of these cytokines on BM stem cells, intrinsic cells, and motor function recovery in spinal cord-injured mice. ⋯ In this study, the combined administration of SCF and G-CSF in traumatic spinal cord injury not only improved motor function, but also induced the accumulation of intrinsic microglia and the active proliferation of intrinsic oligodendrocyte precursor cells.