AI Article Synopsis

  • Bertolotti syndrome (BS) is a condition often overlooked in young people with chronic lower back pain, linked to unusual lumbosacral vertebrae.
  • A case study of a 19-year-old woman showed BS was diagnosed after imaging confirmed fusion of a vertebra, leading to significant pain and movement restrictions.
  • The patient opted for conservative treatment with medication and exercise, resulting in a full recovery at the six-month follow-up, highlighting the need for better awareness of BS in chronic pain assessments.

Article Abstract

Background: Bertolotti syndrome (BS) is often a missed cause of chronic lower back pain in young individuals, commonly associated with the presence of anomalous lumbosacral transitional vertebrae.

Case Presentation: A 19-year-old female with no significant medical or family history presented with persistent lower back pain localized to the gluteal region and posterolateral aspect of the left lower back. The pain worsened over time and limited their movements, including walking. A Ferguson radiograph revealed fusion of the left transverse process of the L5 vertebral segment with the left sacral ala. History, examination findings, and radiological workup confirmed the diagnosis of BS. The patient preferred conservative management, receiving oral pharmacological therapy for six weeks, along with education on preventive measures and routine exercises for postural stability. At a six-month follow-up, the patient remained asymptomatic and managed well.

Conclusions: Conservative oral pharmacological treatment presents a unique and viable alternative to traditional methods for managing BS, which often involve surgery or steroids/anesthetics at the pseudo-articulation site. Given that BS is common yet underdiagnosed in young patients with chronic back pain, this report also underscores the importance of including it in differential diagnoses for chronic lower back pain in this demographic.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11543497PMC
http://dx.doi.org/10.1016/j.jor.2024.10.028DOI Listing

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