Sato Tatsuya, Yonezawa Ikuho, Onda Shingo, Yoshikawa Kei, Takano Hiromitsu, Shimamura Yukitoshi, Okuda Takatoshi, Kaneko Kazuo
Department of Orthopedic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
Medicine (Baltimore). 2017 Sep;96(36):e7895. doi: 10.1097/MD.0000000000007895.
A hyperlordosis deformity of the lumbar spine is relatively rare, and surgical treatment has not been comprehensively addressed. In this case report, we describe the clinical presentation, surgical treatment, and medium-term follow-up of a patient presenting with a progressive lumbar hyperlordosis deformity after resection of a spinal lipoma associated with spina bifida.
The patient was a 20-year-old woman presenting with a progressive hyperlordosis deformity of the lumbar spine associated with significant back pain (visual analog pain score of 89/100 mm), but with no neurological symptoms.
The lumbar lordosis (LL), measured on standing lateral view radiographs, was 114°, with a sagittal vertical axis (SVA) of -100 mm. The patient had undergone excision of a lipoma, associated with spina bifida of the lumbar spine, at 7 months of age.She was first evaluated at our hospital at 18 years of age for progressive spinal deformity and lumbago.
An in situ fusion, from T5 to S1, using pedicle screws with bone graft obtained from the iliac crest, was performed.
Postoperatively, the LL decreased to 93°, and the SVA decreased to -50 mm. The decision to not correct the hyperlordosis deformity fully was intentional. Seven years and 1 month postsurgery, the patient had no limitations in standing and walking and reported a pain score of 8/100 mm; there was no evidence of a loss of correction.
Lumbar hyperlordosis after resection of a spinal lipoma associated with spina bifida is rare. Posterior fixation provided an effective treatment in this case. As the lumbar hyperlordosis deformity is often high, correction can be difficult. In this case, although the correction and fusion were performed in situ, there was no progression of either the deformity or the lumbago. Early detection remains an essential component of effective treatment, allowing correction when the spinal deformity is easily reversible.
腰椎前凸畸形相对少见,手术治疗尚未得到全面探讨。在本病例报告中,我们描述了一名患者的临床表现、手术治疗及中期随访情况,该患者在切除与脊柱裂相关的脊髓脂肪瘤后出现进行性腰椎前凸畸形。
患者为一名20岁女性,表现为腰椎进行性前凸畸形,伴有严重背痛(视觉模拟疼痛评分89/100mm),但无神经症状。
站立位侧位X线片测量的腰椎前凸(LL)为114°,矢状垂直轴(SVA)为-100mm。患者7个月大时接受了与腰椎脊柱裂相关的脂肪瘤切除术。她18岁时因进行性脊柱畸形和腰痛首次在我院接受评估。
采用取自髂嵴的骨移植,使用椎弓根螺钉进行从T5至S1的原位融合。
术后,LL降至93°,SVA降至-50mm。不完全矫正前凸畸形是有意决定的。术后7年1个月,患者站立和行走无限制,疼痛评分为8/100mm;无矫正丢失的证据。
与脊柱裂相关的脊髓脂肪瘤切除术后的腰椎前凸罕见。后路固定在本病例中提供了有效的治疗。由于腰椎前凸畸形通常较高,矫正可能困难。在本病例中,尽管原位进行了矫正和融合,但畸形和腰痛均未进展。早期发现仍然是有效治疗的重要组成部分,以便在脊柱畸形易于逆转时进行矫正。