Suppr超能文献

累及胸椎的腱鞘巨细胞瘤。

Giant-cell tumor of the tendon sheath involving the thoracic spine.

作者信息

Doita Minoru, Miyamoto Hiroshi, Nishida Kotaro, Nabeshima Yuji, Yoshiya Shinichi, Kurosaka Masahiro

机构信息

Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

J Spinal Disord Tech. 2005 Oct;18(5):445-8. doi: 10.1097/01.bsd.0000154458.70337.c0.

Abstract

Giant-cell tumor of the tendon sheath is a common benign lesion of the synovial membrane that frequently occurs in the hand. It is related to pigmented villonodular synovitis and the occurrence of pigmented villonodular synovitis or giant-cell tumor of the tendon sheath in the axial skeleton is very rare. To data, only three cases of giant-cell tumor of the tendon sheath involving cervical spine have been reported, compared with 26 cases of pigmented villonodular synovitis. Pigmented villonodular synovitis involving the thoracic spine is also extremely rare and our case represents the first reported case of a giant-cell tumor of the tendon sheath involving the thoracic spine. A 26-year-old man presented with left back pain without neurological deficit. Computed tomography and magnetic resonance imaging (MRI) revealed an osteolytic and expansive lesion in the left facet joint between the seventh and eighth thoracic vertebrae. A complete facetectomy and excision of the lesion followed by a posterior arthrodesis between Th5 and Th9 was performed. Postoperatively, the patient recovered with complete relief of symptoms, there was no evidence of recurrent disease or regrowth of the residual lesion, as investigated by plain radiographs and MRI within a follow-up period of two years. Although giant-cell tumor of the tendon sheath in the thoracic spine may be extremely uncommon, it should be considered in the differential diagnosis, especially when a benign lesion appears to originate in the face joint. Considering the high rate of recurrence, every effort should be made to achieve total excision.

摘要

腱鞘巨细胞瘤是滑膜的一种常见良性病变,常发生于手部。它与色素沉着绒毛结节性滑膜炎有关,而色素沉着绒毛结节性滑膜炎或腱鞘巨细胞瘤在中轴骨中极为罕见。截至目前,仅有3例累及颈椎的腱鞘巨细胞瘤病例报道,相比之下,色素沉着绒毛结节性滑膜炎有26例。累及胸椎的色素沉着绒毛结节性滑膜炎也极其罕见,我们的病例是首例报道的累及胸椎的腱鞘巨细胞瘤。一名26岁男性因左侧背痛就诊,无神经功能缺损。计算机断层扫描和磁共振成像(MRI)显示,在第七和第八胸椎之间的左侧小关节处有一个溶骨性、膨胀性病变。进行了完整的小关节切除术和病变切除术,随后在胸5和胸9之间进行了后路关节融合术。术后,患者症状完全缓解,恢复良好。在两年的随访期内,通过X线平片和MRI检查,未发现复发或残留病变再生长的迹象。尽管胸椎腱鞘巨细胞瘤可能极为罕见,但在鉴别诊断时应予以考虑,尤其是当良性病变似乎起源于小关节时。鉴于复发率较高,应尽一切努力实现肿瘤全切。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验