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胸段椎旁平滑肌肉瘤:罕见但确实会发生。

Thoracic paravertebral leiomyosarcoma: rare but it does occur.

作者信息

Aksoy Duygu Yazgan, Altundag M Kadri, Durusu Mine, Abali Huseyin, Onder Sevgen, Turker Alev, Aksoy M Cemalettin, Palaoglu Selçuk

机构信息

Department of Internal Medicine, Hacettepe University School of Medicine, Ankara, Turkey.

出版信息

Spine (Phila Pa 1976). 2002 Jun 15;27(12):E301-3. doi: 10.1097/00007632-200206150-00024.

DOI:10.1097/00007632-200206150-00024
PMID:12065993
Abstract

STUDY DESIGN

Marginal resection of a paraspinal tumor in the thoracic vertebra was performed.

OBJECTIVE

To document a very rare pathology for a paraspinal tumor.

SUMMARY OF BACKGROUND DATA

Primary leiomyosarcoma of the spine or paravertebral space is extremely rare. A case of a patient who was operated on for a mass in the spinal canal and whose pathology was reported to be leiomyosarcoma is presented.

METHODS

Marginal resection of the paravertebral mass was performed.

RESULTS

The pathology of the tumor was reported as leiomyosarcoma.

CONCLUSION

Leiomyosarcomas may develop at any site where smooth muscle cells are present. However, primary leiomyosarcoma of the spine or paravertebral space is extremely rare. Leiomyosarcoma, although rare, should be kept in mind as one of the possible diagnoses when a patient with a paraspinal tumor is presented.

摘要

研究设计

对胸椎旁肿瘤进行边缘切除术。

目的

记录一种非常罕见的脊柱旁肿瘤病理情况。

背景资料总结

脊柱或椎旁间隙的原发性平滑肌肉瘤极为罕见。本文报道了一例因椎管内肿物接受手术治疗且病理报告为平滑肌肉瘤的患者。

方法

对椎旁肿物进行边缘切除术。

结果

肿瘤病理报告为平滑肌肉瘤。

结论

平滑肌肉瘤可发生于任何存在平滑肌细胞的部位。然而,脊柱或椎旁间隙的原发性平滑肌肉瘤极为罕见。虽然罕见,但当出现脊柱旁肿瘤患者时,平滑肌肉瘤应作为可能的诊断之一予以考虑。

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Free disease long-term survival in primary thoracic spine leiomyosarcoma after total en bloc spondylectomy: A case report.全椎体整块切除术后原发性胸椎平滑肌肉瘤的无病长期生存:一例报告
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Primary multiple osseous leiomyosarcomas of the spine metastasizing to the skull.脊柱原发性多骨平滑肌肉瘤转移至颅骨。
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