Paget sarcoma of the spine: Scottish Bone Tumor Registry experience.

Spine (Phila Pa 1976)

Department of Orthopaedic Surgery, Scottish Bone Tumor Registry, Western Infirmary, Glasgow, UK.

Published: May 2006

AI Article Synopsis

  • The study was a retrospective case analysis of 13 patients with Paget sarcoma of the spine, sourced from a larger tumor registry, aimed at understanding clinical, radiologic, and histologic characteristics along with prognostic factors.
  • It highlighted that while Paget disease of bone is common, the sarcomatous degeneration in the spine is rare, with limited literature on its clinical presentation and outcomes.
  • The results showed most patients were older adults with symptoms primarily of back pain and significant neurological issues; the average survival time post-diagnosis was just over 4 months.

Article Abstract

Study Design: Retrospective case study of 13 cases of Paget sarcoma of the spine accrued from a prospectively collected Tumor Registry database.

Objectives: To analyze the clinical, radiologic, and histologic features of Paget sarcoma of the spine and to determine the factors influencing the prognosis.

Summary Of Background Data: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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http://dx.doi.org/10.1097/01.brs.0000218506.72608.49DOI Listing

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