Aims

A variety of surgical methods and strategies have been demonstrated for Andersson lesion (AL) therapy. In 2011, we proposed and identified the feasibility of stabilizing the spine without curettaging the vertebral or discovertebral lesion to cure non-kyphotic AL. Additionally, due to the excellent reunion ability of ankylosing spondylitis, we further came up with minimally invasive spinal surgery (MIS) to avoid the need for both bone graft and lesion curettage in AL surgery. However, there is a paucity of research into the comparison between open spinal fusion (OSF) and early MIS in the treatment of AL. The purpose of this study was to investigate and compare the clinical outcomes and radiological evaluation of our early MIS approach and OSF for AL.

The study was conducted to review the outcome in cases of anterior expandable interbody cages inserted through a posterior only approach. Cases selected were the anterior cage insertion and posterior stabilization patients managed by posterior only approach.

Study includes the patients of various pathologies requiring 3 column support. Twenty patients were included in study. Pathology in 9 patients was tuberculosis, trauma in 3, tumours in 3, metastasis in 3 and deformities in 2patients. Patients with or without neurological deficit were included.

Cases were carefully assessed and patients with single level involvement were included as more then single level involvement required more extensive exposure and possible nerve root sacrifice. Detailed neurological status was recorded. The surgery was performed in prone position and after posterior stabilization by pedicle screws the extracavitatory approach was used to insert the expandable cage. In cases of suspicious pathologies the samples for histopathology and staining were collected.

Morbidity, mortality blood loss, surgical time, complications, outcome of surgery were compared with historical controls of front and back surgery.

The insertion of cages from posterior approach was feasible in all carefully planned cases. None of the patients had problem related to implant in form of cage displacement. All the patients had satisfactory outcome.

Posterior stabilization of spine with expandable cage insertion from posterior approach saves the operating time, spares the additional surgical incision and blood loss without compromising the outcome. In carefully planned surgeries it gives excellent results irrespective of etiology.

Purpose

To describe the frequency of different patterns of pain response and their association with outcomes (prognosis) and MRI findings in patients experiencing sciatica.

Introduction. Adolescent idiopathic scoliosis (AIS) is the most common paediatric spinal deformity, affecting about 3% of school-aged children worldwide. This disorder occurs in otherwise healthy children who bear no obvious deficiencies in the components of the spinal column itself. The cause of AIS is poorly understood, as is implied by the name. Lesions of the bony composition of the vertebrae, the vertebral endplates, the paraspinous muscles, or the neurological system each have been proposed to explain disease pathogenesis. Progress has been hampered by the absence of an obvious AIS animal model. Consequently we have used genetic studies in human populations to identify factors underlying AIS susceptibility. The complex inheritance and population frequency of AIS suggest that many genetic factors are involved in this disease. To search comprehensively for such factors we previously undertook the first genome-wide association study (GWAS) of AIS susceptibility in a cohort of 419 families in Texas, USA. We found that chromosome 3 SNPs in the proximity of the CHL1 gene yielded strongest results, which we replicated in additional cohorts (rs10510181 OR 1·49, 95% CI 1·29–173, p=2·58×10–8). CHL1 is of interest because it encodes an axon guidance protein and is functionally related to the ROBO3 gene that causes hereditary gaze palsy with progressive scoliosis (HGPPS), a rare disease marked by severe scoliosis. Here we expanded the study to 702 Texas families. Methods. We tested more than 327 000 single-nucleotide polymorphisms (SNPs) across all human autosomes for association with disease. Results. Results of the study in 702 Texas families yielded evidence for association with SNPs in a second axon guidance gene, DSCAM, which encodes a protein in the same structural and functional class with Chl1 and Robo3 (rs2222973 combined OR 0·59, 95% CI 0·48–0·74; p=1·46×10–6). We additionally found AIS associations with loci in CNTNAP2, whose protein product interacts directly with L1 and Robo class proteins and participates in axon pathfinding. Conclusions. These data support genetic variation in axon guidance genes as risk factors in AIS. Our results provide new insight into disease pathogenesis and suggest that late-onset scoliosis may be correlated with secondary neurological development