Study Design: Retrospective study of 146 patients with the diagnosis of occipitalization, atlantoaxial dislocation (AAD) and basilar invagination, using a novel surgical treatment strategy.
Objective: To introduce a novel fixation and reduction technique.
Summary Of Background Data: Atlas occipitalization associated with basilar invagination often result in fixed AAD that need reduction and occipitocervical fixation. The widely used occipitocervical fixation with suboccipital screws has several limitations such as the poor screw purchase in maldevelopment of the occipital bone, limited area available for implants in previous suboccipital craniectomy. The placement of occipitalized C1 lateral mass screw is an alternative option.
Methods: From June 2007 to June 2013, 146 patients of occipitalized atlas with fixed AAD and basilar invagination, underwent fixation and reduction via C1 lateral mass and C2 pars/pedicle screw.
Results: A total of 143 patients achieved the follow-up in the range from 6 months to 4 years (average, 30 mo). Neurological improvement was seen in all the 143 patients, with the averaged Japanese Orthopedic Association scores increasing from 11.6 to 15.5. Radiographical evaluation showed that solid bony fusion was achieved in all patients, and complete reduction was attained in 95 patients, and partial reduction (>60%) in 40 patients, and no effective reduction in 8 patients who had additional transoral decompression. Magnetic resonance imaging demonstrated that the ventral cervicomedullary compression was relieved in all patients.
Conclusion: Although technically demanding, the C1 lateral mass placement in occipitalization is very useful in the rescue situation where more conventional stabilization alternatives are not technically possible, or as routine occipitocervical stabilization. It provides firm stabilization offering an optimum situation for bony fusion, and meanwhile the effective reduction of fixed AAD and basilar invagination. An extremely high fusion rate can be expected with minimal complications and minimal postoperative immobilization with this technique.
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http://dx.doi.org/10.1097/BRS.0000000000000611 | DOI Listing |
Childs Nerv Syst
December 2024
NJ Craniofacial Center, Morristown, NJ, 07960, USA.
Background: Goldenhar syndrome is a clinically heterogeneous disorder defined by a rare combination of congenital anomalies-an eye abnormality, in addition to two of the following three: ear anomalies, mandibular malformations, and vertebral defects. Notably, children with Goldenhar syndrome present with a high incidence of cervical spine malformations.
Clinical Case: In this report, we present an unusual case of a 15-year-old child with Goldenhar syndrome, who additionally presents with some clinical features of VACTERL syndrome.
Neurochirurgie
December 2024
Aix Marseille Univ, APM, UH Timone, Department of Neurosurgery, Marseille, France.
Background: The Da Vinci robot ® (DVR), released in the early 2000s, provided a set of innovation aiming at pushing minimally invasive surgery forward. Its stereoscopic magnified visualization camera, motions that exceed the natural range of the human hand, or tremor reduction enhanced the surgeon's skills and added value in many surgical fields.
Objective: To map the current use of the DVR in spine surgery, identify gaps, address its limits and future perspectives.
BMJ Case Rep
December 2024
McMaster Children's Hospital/ Hamilton Health Sciences, Hamilton, Ontario, Canada.
This case report describes the clinical journey of a male patient in early childhood with developmental delay, failure to thrive, worsening right-sided head tilt torticollis and regression of motor skills with spasticity of the lower limbs. The case was complex due to the early onset and gradually worsening symptoms, including a decline in established motor milestones. Genetic testing to investigate the delayed neurodevelopment revealed a variant that did not fully explain the patient's phenotype.
View Article and Find Full Text PDFSurg Neurol Int
November 2024
Department of Neurosurgery, National Ribat University, Khartoum, Sudan.
Background: The surgery on the craniocervical junction is associated with complex techniques that endanger the vertebral artery (VA), especially if there are some anatomical variations present, thereby increasing the risk of vascular injury, particularly during cervical decompression or instrumentation.
Case Description: A case of a 60-year-old female with progressive myelopathy and craniocervical junction malformation is presented. Key preoperative imaging findings included basilar invagination, C1 assimilation, and os odontoideum, along with VA anomalies such as a tortuous, hypoplastic left VA arising anomalously from the aortic arch and a right VA with a V2 segment forming a high-riding medial loop into the C2 vertebral body.
Neurol India
November 2024
Department of Neurosurgery, K.E.M. Hospital and Seth G.S. Medical College, Parel, Mumbai, Maharashtra, India.
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