| Literature DB >> 33088418 |
Justin Cole1, Fadi Nemeh1, Achint K Singh1, Jason Lally1.
Abstract
Intervertebral disc calcification is rare in the pediatric population and is associated with sudden neurological manifestations. Although commonly symptomatic, conservative management yields excellent prognosis in the vast majority of cases. The following case illustrates the finding of intervertebral disc calcification in a patient with vertebral body segmentation anomaly consistent with Klippel-Feil Syndrome. As both entities are associated with potential neurological sequelae, this case of coexistent pathologies highlights the importance of recognizing the potential presence of intervertebral disc calcifications in pediatric Klippel-Feil Syndrome patients. Copyright Journal of Radiology Case Reports.Entities:
Keywords: Cervical spinal stenosis; Computed Tomography; Intervertebral disc calcification; Klippel-Feil Syndrome; Ossified posterior longitudinal ligament
Mesh:
Year: 2020 PMID: 33088418 PMCID: PMC7536000 DOI: 10.3941/jrcr.v14i8.3790
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922