Chang Sheng, Wang Yu, Liu Yong, Wang Chao
Department of Spine Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.
Department of Surgery, Kashgar Hospital of Chinese Medicine, Kashgar, the Xinjiang Uygur Autonomous Region, China.
Front Surg. 2024 Jun 28;11:1357282. doi: 10.3389/fsurg.2024.1357282. eCollection 2024.
The causes of pedicle cleft include congenital dysplasia and stress fractures, both of which are rare conditions. Secondary lumbar spondylolisthesis with combined unilateral pedicle cleft and contralateral spondylolysis is extremely rare and can be easily misdiagnosed. We report two cases with these conditions from different causes and discuss the diagnostic and therapeutic features in the context of the literature review.
Case 1 was a 58-year-old female with a stress fracture change at the left L5 pedicle. Case 2 was a 47-year-old female with a pedicle cleft due to hypoplasia of the left L5 pedicle. Both patients had a combined contralateral spondylolysis and Meyerding grade one lumbar spondylolisthesis, while neither had a clear history of lumbar trauma. After initial conservative treatments failed, both patients underwent a single-segment posterior lumbar interbody fusion with bilateral pedicle screw fixation. Both patients were followed up for more than 1 year postoperatively with clinical symptom relief and bony fusion at the pedicle cleft suggested by a CT scan.
Lumbar spondylolisthesis with unilateral pedicle cleft and contralateral spondylolysis is rarely reported and can be clinically misdiagnosed as simple spondylolisthesis with bilateral spondylolysis. There is no widely accepted surgical option for patients for whom conservative treatment has failed. Our experience suggests that good clinical results may be achieved by single-segment posterior interbody fusion and bilateral pedicle screw fixation. Precise screw placement into the deficient pedicle and sufficient exiting nerve decompression are prerequisites for the success of this surgical option.
椎弓根裂的病因包括先天性发育异常和应力性骨折,这两种情况均较为罕见。合并单侧椎弓根裂和对侧椎弓峡部裂的继发性腰椎滑脱极为罕见,且易被误诊。我们报告两例病因不同的此类病例,并结合文献复习讨论其诊断和治疗特点。
病例1为一名58岁女性,左侧L5椎弓根有应力性骨折改变。病例2为一名47岁女性,因左侧L5椎弓根发育不全导致椎弓根裂。两名患者均合并对侧椎弓峡部裂和迈尔丁I度腰椎滑脱,且均无明确的腰部外伤史。初始保守治疗失败后,两名患者均接受了单节段后路腰椎椎间融合术并双侧椎弓根螺钉固定。两名患者术后均随访1年以上,临床症状缓解,CT扫描提示椎弓根裂处有骨融合。
单侧椎弓根裂合并对侧椎弓峡部裂的腰椎滑脱鲜有报道,临床上易被误诊为双侧椎弓峡部裂的单纯腰椎滑脱。对于保守治疗失败的患者,尚无广泛接受的手术方案。我们的经验表明,单节段后路椎间融合术和双侧椎弓根螺钉固定可能取得良好的临床效果。将螺钉精确置入缺损的椎弓根并充分减压出口神经是该手术成功的前提条件。