Kim Sang Woo, Kim Min Su, Jung Young Jin
Department of Neurosurgery, College of Medicine, Yeungnam University, Daegu, Korea.
J Korean Neurosurg Soc. 2013 Jan;53(1):46-8. doi: 10.3340/jkns.2013.53.1.46. Epub 2013 Jan 31.
Chondrosarcoma is a very uncommon malignant primary bone tumor, especially, it occurs extremely rare in the spine. A 52-year-old man was admitted to the emergency room with sudden paraplegia. Twelve hours prior to a paraplegic event, he visited an outpatient clinic with discomfort and tenderness around the medial border of the right scapular, and his neurologic status was absolutely intact. Magnetic resonance imaging showed a lobulated soft tissue mass from T3 to T5, which extended to the epidural space. Computed tomography scans showed soft tissue mass on the spinal posterior arch and osteolytic change of the adjacent bony structures. Emergent surgery was performed and the lesion was removed. Dark reddish blood and gel-like material were encountered around the dura and posterior arch during the operation. Multiple pulmonary nodules were found on a chest CT scan and a biopsy of one of them had been proven to be a metastasis of chondrosarcoma. The histologic examination showed dedifferentiated chondrosarcoma. The patient's neurologic deficit was improved slowly from ASIA A to ASIA D. Chondrosarcoma in the spine is extremely rare, even more with acute hemorrhage and sudden expansion into the epidural space. We named it chondrosarcoma apoplexy. We should consider the possibility of a hemorrhagic event when the patient's neurologic deficit worsens suddenly with spinal bone tumor.
软骨肉瘤是一种非常罕见的原发性恶性骨肿瘤,尤其是在脊柱中极为罕见。一名52岁男性因突发截瘫入住急诊室。在截瘫事件发生前12小时,他因右肩胛内侧缘周围不适和压痛前往门诊就诊,当时其神经功能完全正常。磁共振成像显示T3至T5水平有一个分叶状软组织肿块,延伸至硬膜外间隙。计算机断层扫描显示脊柱后弓有软组织肿块以及相邻骨质结构的溶骨性改变。遂行急诊手术并切除病变。术中在硬膜和后弓周围发现暗红色血液和凝胶状物质。胸部CT扫描发现多个肺结节,其中一个活检已证实为软骨肉瘤转移。组织学检查显示为去分化软骨肉瘤。患者的神经功能缺损从美国脊髓损伤协会(ASIA)分级A缓慢改善至ASIA D级。脊柱软骨肉瘤极为罕见,更罕见的是伴有急性出血并突然扩展至硬膜外间隙。我们将其命名为软骨肉瘤卒中。当患者因脊柱骨肿瘤突然出现神经功能缺损恶化时,应考虑出血事件的可能性。