Reynolds Jeremy J, Rothenfluh Dominique A, Athanasou Nick, Wilson Shaun, Kieser David C
Division of Spinal Surgery, University of Oxford, Oxford, England, UK.
Department of Orthopaedic Surgery and Musculoskeletal Medicine, Canterbury District Health Board, 2 Riccarton Avenue, Christchurch, 8011, New Zealand.
Eur Spine J. 2018 Jul;27(Suppl 3):446-452. doi: 10.1007/s00586-018-5461-z. Epub 2018 Jan 22.
To present a case of aggressive sacral osteoblastoma (OB) treated with neoadjuvant denosumab therapy and en bloc resection.
Case report of a 14-year-old male with an aggressive OB affecting the superior articular process of the left first sacral segment. The lesion was lytic and metabolically active and involved the left-sided posterior elements of S1-S3 with extension into the spinal canal, affecting the left S1, S2, S3, S4 and S5 nerve roots. He was treated for 1 month with neoadjuvant denosumab followed by en bloc resection.
Denosumab therapy caused regression of the tumour and converted the diffuse infiltrative mass into a well-defined solid (osteoma-like) structure, aiding surgical resection and preserving the S1, S4 and S5 nerve roots. Histologically, the treated lesion showed abundant sclerotic woven bone and osteoblasts with absence of osteoclasts.
A short course of denosumab caused tumour regression, ossification and conversion of an aggressive OB into a sclerotic, well-defined lesion thus aiding surgical resection and preservation of neural structures. Neoadjuvant therapy reduced osteoclast numbers but PET showed that the lesion remained FDG avid post-therapy.
介绍1例采用新辅助地诺单抗治疗并整块切除的侵袭性骶骨骨母细胞瘤(OB)病例。
报告1例14岁男性侵袭性OB病例,累及左侧第一骶椎节段的上关节突。病变呈溶骨性且代谢活跃,累及S1 - S3左侧后部结构并延伸至椎管,影响左侧S1、S2、S3、S4和S5神经根。先给予新辅助地诺单抗治疗1个月,随后进行整块切除。
地诺单抗治疗使肿瘤缩小,将弥漫性浸润性肿块转变为边界清晰的实性(骨瘤样)结构,有助于手术切除并保留S1、S4和S5神经根。组织学检查显示,治疗后的病变有大量硬化编织骨和成骨细胞,无破骨细胞。
短期应用地诺单抗可使肿瘤缩小、骨化,将侵袭性OB转变为硬化性、边界清晰的病变,从而有助于手术切除和保留神经结构。新辅助治疗减少了破骨细胞数量,但PET显示治疗后病变仍摄取FDG。