Introduction: Spinopelvic malalignment causes continual backache. Intervertebral Disc Degeneration (IDD) is a leading cause of low backache. Understanding the relationship between spinopelvic parameters and IDD can help with better diagnosis and treatment and avoid unnecessary investigations. Aim: To measure radiographic spinopelvic parameters of patients diagnosed with varying grades of IDD in the lumbosacral spine on Magnetic Resonance Imaging (MRI), and to compare them with radiographs of the asymptomatic population (controls). Materials and Methods: A hospital-based retrospective observational study was done from January 2021 to August 2022 at a tertiary care hospital in Uttar Pradesh, India with 80 patients diagnosed with IDD on MRI and 80 controls. Cases were defined as patients diagnosed to have IDD on MRI and controls were those individuals who did not have disc degeneration on MRI. Lateral lumbosacral spine radiographs were taken, and spinopelvic parameters {Pelvic Tilt (PT), Sacral Slope (SS), Pelvic Incidence (PI), Lumbar Lordosis (LL), lumbo-sacral angle, and sacral horizontal angle} were measured using Surgimap Spine Software. T-test and Chi-square test were used for comparison between cases and controls. Results: Six patients had asymmetric disc bulge, 11 had symmetric disc bulge, 18 had disc extrusion and 45 had disc protrusion. Mean PT in patients with IDD was 11.05±3.84°, and control was 8.65±3.19°, p-value=0.009. Mean SS in case group was 38.38±3.03° and control was 36.56±3.43°, p-value=0.031. The mean PI of cases was 49.44±8.39° and control 46.19±9.01°, p-value=0.02. LL angle was higher in IDD at 46.34°, and was 45.36° in healthy individuals, without statistically significant difference. The mean lumbo-sacral angle in both study groups was similar. The mean Sacral Inclination Angle (SIA) was found to be 43.99° and 44.96° in the case and control group respectively without showing significant differences. A statistically significant difference was found only for the comparison of PT between different grades of IDD (p-value=0.039). Conclusion: Using Surgimap Spine Software, one can predict the individuals that possess a greater propensity of developing degeneration of disc and chronic low back pain in a more costeffective manner.

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Background: Congenital Central Nervous System (CNS) anomalies have typical and characteristic imaging features. Imaging plays a pivotal role in their diagnosis. This study aims to determine the prevalence and spectrum of the various congenital anomalies of the CNS diagnosed at our institution, and to classify the imaging features according to an approved classification system.Methods: This cross-sectional study was conducted on infants and children below 12 years of age attending the Department of Radiodiagnosis of our Institution, for radiographic investigation of congenital anomalies in CNS through Computerised Tomography and/or Magnetic Resonance Imaging, over a period of one year. The spectrum of imaging features was analysed as per approved classification and corroboration with their clinical background. The prevalence of each type of congenital anomaly was also assessed.Results: A total number of 43 developmental anomalies of the central nervous system were encountered in 33 patients over a period of one year. The most common anomalies encountered were partial corpus callosal agenesis, heterotopic grey matter and Dandy Walker malformation. The total prevalence of CNS anomalies was 4.22%. The most common clinical symptoms in these patients were seizures followed by focal neurological deficit. The imaging findings of each anomaly are discussed.Conclusions: Developmental anomalies of CNS are encountered in 4.22% of patients in our Institution, with partial corpus callosum agenesis being the most frequent entity. Familiarity with imaging findings of these malformations is mandatory for every radiologist.

Background: Astroblastoma is rare neuroglial intracranial tumor most commonly occurring in the first three decades of life. Case report: A 5 year old female child presented with intermittent headache, diplopia and recurrent seizures over a period of approximately 4 months. Her neurological examination revealed 6 th nerve palsy and papilledema. Both CT and MRI revealed a well defined enhancing solid-cystic mass in the left fronto-parietal cerebral cortex with mass effect suggestive of primitive neuroectodermal tumor. She underwent gross total resection of the lesion through craniotomy. Histopathology along with immunohistochemistry was surprisingly suggestive of astroblastoma. Conclusion: Astroblastomas are very rare and often misdiagnosed.