Hoffpauir Lauren N, Olexo Rob, Hamric Hiliary
Research, West Virginia School of Osteopathic Medicine, Lewisburg, USA.
Family Medicine, West Virginia School of Osteopathic Medicine, Lewisburg, USA.
Cureus. 2025 Feb 24;17(2):e79576. doi: 10.7759/cureus.79576. eCollection 2025 Feb.
Bertolotti's syndrome is a condition characterized by mechanical low back pain due to a congenital transitional lumbosacral segment of L5-S1. Diagnosis can be challenging for physicians because it requires the presence of both a transitional vertebrae and pain that is directly attributed to this genetic anomaly. This case report describes an adolescent case of Bertolotti's syndrome seen in a 17-year-old male who presents with several months of low back pain associated with squatting and bending over. His pain was ultimately diagnosed through lumbar radiographs, which demonstrated a transitional L5 vertebrae. Treatment of Bertolotti's syndrome is dependent on the severity of the symptoms, with options starting conservatively through the use of non-steroidal anti-inflammatory drugs (NSAIDs) and lifestyle modifications to invasive approaches such as nerve ablation or surgical spinal fusion. Bertolotti's syndrome is rarely diagnosed in children, as most cases of pain begin in early adulthood. However, early recognition in young patients allows for more precisely guided treatments and optimal pain management.
贝托洛蒂综合征是一种由于L5 - S1先天性腰骶移行节段导致机械性下腰痛的病症。对医生来说,诊断可能具有挑战性,因为它需要同时存在移行椎骨以及直接归因于这种基因异常的疼痛。本病例报告描述了一名17岁男性青少年的贝托洛蒂综合征病例,该患者出现了数月与蹲姿和弯腰相关的下腰痛。他的疼痛最终通过腰椎X线片得以诊断,该片显示有L5移行椎骨。贝托洛蒂综合征的治疗取决于症状的严重程度,治疗选择从保守治疗开始,包括使用非甾体抗炎药(NSAIDs)和改变生活方式,到侵入性方法,如神经消融或脊柱手术融合。贝托洛蒂综合征在儿童中很少被诊断出来,因为大多数疼痛病例始于成年早期。然而,在年轻患者中早期识别有助于进行更精确的针对性治疗和优化疼痛管理。