Department of Biology, University of North Florida, Jacksonville, FL 32224, USA.
Spine J. 2010 Jul;10(7):e6-e10. doi: 10.1016/j.spinee.2010.04.013. Epub 2010 May 20.
Vertebral osteolysis has been reported as a complication of off-label recombinant human bone morphogenetic protein-2 (rhBMP-2) use in transforaminal lumbar interbody fusion (TLIF). It has been postulated that end plate violation during disc space preparation, rhBMP-2 overdosing, or a combination thereof can contribute to the development of vertebral osteolysis when rhBMP-2 is used in the lumbar interspace.
To present two cases of vertebral osteolysis that occurred after TLIF in which rhBMP-2 was used. In each case, the osteolysis originated from subchondral cysts that were present on preoperative computed tomographic (CT) scans.
Case report.
Two patients underwent instrumented TLIF using INFUSE (Medtronic, Inc., Littleton, MA, USA) on an absorbable collagen sponge carrier. In each patient, approximately 4 mg of rhBMP-2 was placed anteriorly in the disc space with 0.1 mg of rhBMP-2 being placed inside a polyetheretherketone interbody cage. Morcellized allograft bone mixed with demineralized bone matrix was also placed in the disc space and cage. The remaining rhBMP-2 was placed posterolaterally on the contralateral side. Each patient presented with worsening back pain approximately 3 to 4 months postoperatively and CT scans revealed osteolysis affecting the L4 and L5 vertebral bodies. The osteolysis appeared to originate from preoperative vertebral defects caused by subchondral cysts.
One patient underwent removal of the interbody cage at the L4-L5 level and revision of the fusion with iliac crest autograft. At 15-month follow-up, he had no complaints of back pain, and CT scanning revealed solid fusion across the L4-L5 disc space. The other patient was offered revision of his fusion but declined any further surgery. At 2-year follow-up, that patient had persistent back pain but still declined any further surgery. A CT scan revealed unchanged osteolysis at the L4 and L5 levels.
It has been proposed that rhBMP-2-induced vertebral osteolysis occurring in TLIF procedures may be secondary to end plate violation during disc preparation or overdosing of rhBMP-2. Although overdosing may have also contributed to vertebral osteolysis in our two cases, the end plate violation from subchondral cyst formation that was present on preoperative CT scans seemed to be the origin of the osteolysis suggesting that the presence of preoperative subchondral cysts may be an additional risk factor for development of osteolysis in these patients.
已有研究报道,在经椎间孔腰椎间融合术(TLIF)中使用未经批准的重组人骨形态发生蛋白-2(rhBMP-2)会导致椎体溶骨。据推测,在椎间盘间隙准备过程中破坏终板、rhBMP-2 超剂量使用或两者结合,均可能导致 rhBMP-2 用于腰椎间隙时发生椎体溶骨。
报告两例使用 rhBMP-2 后发生的 TLIF 后椎体溶骨病例。在每个病例中,溶骨均源自术前 CT 扫描显示的软骨下囊肿。
病例报告。
两名患者接受了 INFUSE(Medtronic,Inc.,马萨诸塞州利特尔顿)联合可吸收胶原海绵载体的经皮 TLIF。在每位患者中,约 4 mg rhBMP-2 被置于椎间盘前部,0.1 mg rhBMP-2 被置于聚醚醚酮椎间笼内。还将颗粒状同种异体骨与脱钙骨基质混合后置于椎间盘和笼内。剩余的 rhBMP-2 被置于对侧的椎旁。每位患者术后约 3-4 个月出现背痛加重,CT 扫描显示 L4 和 L5 椎体溶骨。溶骨似乎源自术前由软骨下囊肿引起的椎体缺陷。
一名患者行 L4-L5 水平椎间笼取出和髂嵴自体骨移植翻修融合术。15 个月随访时,患者无腰痛症状,CT 扫描显示 L4-L5 椎间盘间隙融合牢固。另一名患者接受了融合翻修的建议,但拒绝了进一步的手术。2 年随访时,该患者仍有持续性腰痛,但仍拒绝进一步手术。CT 扫描显示 L4 和 L5 水平的溶骨无变化。
据报道,TLIF 术中发生的 rhBMP-2 诱导的椎体溶骨可能是由于椎间盘准备过程中破坏终板或 rhBMP-2 超剂量使用所致。尽管在我们的两个病例中,rhBMP-2 超剂量使用可能也是导致椎体溶骨的原因之一,但术前 CT 扫描显示的软骨下囊肿形成导致的终板破坏似乎是溶骨的起源,提示术前软骨下囊肿的存在可能是这些患者发生溶骨的另一个危险因素。