Matsuda Yoshiro, Sakayama Kenshi, Sugawara Yoshifumu, Miyawaki Joji, Kidani Teruki, Miyazaki Tatsuhiko, Tanji Nozomu, Yamamoto Haruyasu
Department of Orthopaedic Surgery, Ehime University School of Medicine, Ehime, Japan.
Spine (Phila Pa 1976). 2006 Apr 15;31(8):E231-6. doi: 10.1097/01.brs.0000210297.02677.66.
A case report of an extremely rare malignant spinal tumor successfully treated with total en bloc spondylectomy and chemotherapy.
To describe points for consideration when an osteogenic lesion in the spine is diagnosed and treated.
Primary mesenchymal chondrosarcoma in the spine is extremely rare. There were no reports of this tumor being treated with spondylectomy to achieve total surgical resection with a wide margin followed by chemotherapy.
A 44-year-old female presented with low back pain and left flank pain. Magnetic resonance imaging and computerized tomography showed an osteosclerotic tumor of the lumbar vertebrae. Tc-99m HMDP bone scintigraphy was positive, but thallium-201 scintigraphy and gallium scintigraphy were negative. The patient was diagnosed as having chondrosarcoma based on biopsy findings.
To resect the tumor completely, total en bloc spondylectomy for 2 consecutive lumbar vertebrae was performed. However, the postoperative pathologic diagnosis was extremely difficult because the patient was initially suspected to have osteosarcoma, but the final diagnosis was mesenchymal chondrosarcoma. Five years after surgery, there have not been any signs of local recurrence or distant metastasis, and the patient has remained continuously disease free.
To our knowledge, we reported the first case of mesenchymal chondrosarcoma occurring from the lumbar spine treated with total en bloc spondylectomy and chemotherapy. Successful radical resection of the tumor could be accomplished. Although the effect of chemotherapy on the final results could not be clearly determined, considering that at least continuous disease-free survival was achieved, it is highly likely that chemotherapy contributed to the favorable results.
一例极其罕见的恶性脊柱肿瘤经整块全脊椎切除术和化疗成功治疗的病例报告。
描述诊断和治疗脊柱成骨性病变时需考虑的要点。
脊柱原发性间叶性软骨肉瘤极其罕见。此前尚无关于采用全脊椎切除术实现广泛切缘的肿瘤完全切除并继以化疗治疗该肿瘤的报道。
一名44岁女性出现腰痛和左侧胁腹疼痛。磁共振成像和计算机断层扫描显示腰椎有一个骨硬化性肿瘤。锝-99m亚甲基二膦酸盐骨闪烁显像呈阳性,但铊-201闪烁显像和镓闪烁显像呈阴性。根据活检结果,该患者被诊断为软骨肉瘤。
为完整切除肿瘤,对连续两节腰椎实施了整块全脊椎切除术。然而,术后病理诊断极具难度,因为患者最初被怀疑患有骨肉瘤,但最终诊断为间叶性软骨肉瘤。术后五年,未出现任何局部复发或远处转移迹象,患者一直无病生存。
据我们所知,我们报告了首例采用整块全脊椎切除术和化疗治疗的腰椎间叶性软骨肉瘤病例。肿瘤得以成功根治性切除。尽管化疗对最终结果的影响尚无法明确确定,但鉴于至少实现了持续无病生存,化疗极有可能促成了良好的治疗效果。