Department of Orthopaedic Surgery, Shiga University of Medical Science, Tsukinowa-cho, Seta, Otsu, Shiga, Japan.
Spine J. 2011 May;11(5):e13-8. doi: 10.1016/j.spinee.2011.03.015. Epub 2011 Apr 16.
Osteoid osteoma is a rare benign osteoblastic tumor. Approximately 10% to 20% of osteoid osteomas occur in the spine with a high trend to involve the posterior components; in turn, vertebral body involvement is uncommon. Osteoid osteoma has been classified into cortical, cancellous, and subperiosteal subtypes according to the localization of the nidus. Subperiosteal osteoid osteoma is extremely rare and has been reported mainly in the femoral neck and small bones of the hands and feet. To the best of our knowledge, subperiosteal osteoid osteoma arising in spine has never been reported previously.
To illustrate a rare case of a 23-year-old female with painful scoliosis because of subperiosteal osteoid osteoma of ninth thoracic vertebra that was treated by thoracoscopic intervention.
STUDY DESIGN/SETTING: A case report and review of literature.
Magnetic resonance imaging revealed the inflammation/edema pattern intensity at right side of both 9th and 10th thoracic vertebrae. Computed tomography demonstrated the round radiolucency surrounded by reactive bone formation (nidus) at the right anterolateral aspect of ninth thoracic vertebra. Taken all findings including anatomical localization of the lesion into consideration, we decided to use thoracoscopic intervention. Improvement of scoliosis was achieved 2 months after surgery. At the time of final follow-up, the patient was free of symptom and there was no clinical and radiologic evidence of recurrence of the tumor 1.5 years postoperatively.
Thoracoscopic intervention achieved en bloc extirpation of the nidus after partial removal of the 10th rib head. Thoracoscopic treatment has never been reported as a treatment modality of spinal osteoid osteoma. Within a few hours after the operation, the pain disappeared completely. Histopathological examination revealed that extracted lesion was compatible with osteoid osteoma.
The lesion described here demonstrates an extremely rare variety of spinal osteoid osteoma, which was successfully treated by an unprecedented thoracoscopic intervention. This alternative surgical approach enabled en bloc extirpation and effective correction of scoliosis while achieving a cosmetic satisfaction.
骨样骨瘤是一种罕见的良性成骨细胞瘤。约 10%-20%的骨样骨瘤发生在脊柱,且倾向于累及脊柱后部结构;相反,椎体受累并不常见。根据病灶的定位,骨样骨瘤可分为皮质型、松质骨型和骨膜下型。骨膜下骨样骨瘤极为罕见,主要见于股骨颈和手足小骨。据我们所知,脊柱的骨膜下骨样骨瘤以前从未报道过。
阐述一例 23 岁女性因第九胸椎骨膜下骨样骨瘤引起的疼痛性脊柱侧凸,通过胸腔镜干预进行治疗。
研究设计/设置:病例报告及文献复习。
磁共振成像显示双侧第 9 胸椎和第 10 胸椎右侧炎症/水肿模式强度。计算机断层扫描显示第 9 胸椎右侧前外侧有圆形透亮区,周围有反应性骨形成(病灶)。考虑到所有的发现,包括病变的解剖定位,我们决定采用胸腔镜干预。手术后 2 个月,脊柱侧凸得到改善。在最后一次随访时,患者无任何症状,术后 1.5 年无肿瘤复发的临床和影像学证据。
胸腔镜干预在部分切除第 10 肋骨头后,整块切除了病灶。胸腔镜治疗从未被报道为脊柱骨样骨瘤的治疗方法。术后数小时内,疼痛完全消失。组织病理学检查显示提取的病变与骨样骨瘤相符。
此处描述的病变表现为一种极其罕见的脊柱骨样骨瘤,通过前所未有的胸腔镜干预成功治疗。这种替代的手术方法能够整块切除病灶,有效矫正脊柱侧凸,并获得美容满意度。