Sharma Himanshu, Mehdi S A, MacDuff E, Reece A T, Jane M J, Reid R
Department of Orthopaedic Surgery, Scottish Bone Tumor Registry, Western Infirmary, Glasgow, UK.
Spine (Phila Pa 1976). 2006 May 20;31(12):1344-50. doi: 10.1097/01.brs.0000218506.72608.49.
Retrospective case study of 13 cases of Paget sarcoma of the spine accrued from a prospectively collected Tumor Registry database.
To analyze the clinical, radiologic, and histologic features of Paget sarcoma of the spine and to determine the factors influencing the prognosis.
Paget disease of bone is a common disorder with the spine being involved in over 50% of patients. However, sarcomatous degeneration in the vertebral column is an extremely rare complication. There is very little in the literature with regard to clinical presentation and prognosis of patients with Paget sarcoma affecting the vertebral column.
Between January 1944 and December 2003, 89 patients were registered with a diagnosis of Paget sarcoma in the Scottish Bone Tumor Registry. Thirteen patients with Paget sarcoma of the spine were analyzed with regard to their clinical, radiologic, and histopathologic features along with the prognostic predictors.
The mean age was 66.9 years (range: 56-79 years). There were 10 males and three females. There were seven cases involving the sacral spine (63.6%), three cases involving lumbar vertebrae, two affecting the dorsal spine, and one with diffuse dorsolumbar involvement (D11-L3). The mode of presentation was progressively increasing low back pain (in all 13), unilateral sciatica (six; left-sided, five; right-sided, one), bilateral sciatica (two), lower limb weakness (eight), and autonomic dysfunction (four). Ten of 13 cases (76.9%) were osteosarcoma. The rest were chondrosarcoma (n = 1), fibrosarcoma (n = 1), and malignant fibrous histiocytoma (n = 1). Decompression laminectomy was performed in three patients with progressive neurologic deficit. Eight patients had received radiotherapy. The mean survival was 4.22 months.
This series confirmed that Paget sarcoma of the spine has a very poor prognosis. We found a constellation of symptomatology in patients with sarcomatous Paget spine resulting from radiculomedullary compression, primarily lumbosacral involvement and predominantly osteosarcomatous histology. There was no significant difference observed on the overall prognosis of the patients with Paget sarcoma of the spine in the last 6 decades.
对前瞻性收集的肿瘤登记数据库中累积的13例脊柱佩吉特肉瘤病例进行回顾性病例研究。
分析脊柱佩吉特肉瘤的临床、放射学和组织学特征,并确定影响预后的因素。
骨佩吉特病是一种常见疾病,超过50%的患者脊柱受累。然而,脊柱肉瘤样变性是一种极其罕见的并发症。关于脊柱佩吉特肉瘤患者的临床表现和预后,文献报道极少。
1944年1月至2003年12月期间,89例诊断为佩吉特肉瘤的患者在苏格兰骨肿瘤登记处登记。对13例脊柱佩吉特肉瘤患者的临床、放射学和组织病理学特征以及预后预测因素进行分析。
平均年龄为66.9岁(范围:56 - 79岁)。男性10例,女性3例。7例累及骶椎(63.6%),3例累及腰椎,2例累及胸椎,1例为弥漫性胸腰段受累(D11 - L3)。临床表现为下腰痛进行性加重(13例均有)、单侧坐骨神经痛(6例;左侧5例,右侧1例)、双侧坐骨神经痛(2例)、下肢无力(8例)和自主神经功能障碍(4例)。13例中有10例(76.9%)为骨肉瘤。其余为软骨肉瘤(1例)、纤维肉瘤(1例)和恶性纤维组织细胞瘤(1例)。3例有进行性神经功能缺损的患者接受了减压椎板切除术。8例患者接受了放疗。平均生存期为4.22个月。
本系列研究证实脊柱佩吉特肉瘤预后极差。我们发现肉瘤样佩吉特脊柱患者存在一系列症状,主要由神经根脊髓受压引起,主要累及腰骶部,组织学类型以骨肉瘤为主。在过去60年中,脊柱佩吉特肉瘤患者的总体预后无显著差异。