Hansen Mitchell A, Harper Clive, Yiannikas Con, McGee-Collett Martin
Department of Neurosurgery, Royal Prince Alfred Hospital, Missenden Road, Camperdown NSW 2050, Australia.
J Clin Neurosci. 2007 Apr;14(4):386-8. doi: 10.1016/j.jocn.2005.12.013. Epub 2007 Jan 19.
Tenosynovial giant cell tumours are of two types, localised and diffuse. The diffuse type is also known as pigmented villonodular synovitis (PVNS). There have been 42 previously reported cases of PVNS in the axial skeleton, seven of which were reported in the thoracic spine. A young patient found to have thoracic PVNS and who presented with progressive lower limb weakness and parasthesiae over 3 weeks is reported. Computed tomography and magnetic resonance imaging demonstrated a posterior lesion at T6/7 with local bone invasion. The patient underwent complete resection of the tumour and has had an unremarkable postoperative convalescence with resolution of his signs and symptoms. Total surgical resection is the treatment of choice for this condition and close postoperative follow-up with serial imaging is important to monitor for local recurrence.
腱鞘巨细胞瘤有两种类型,局限性和弥漫性。弥漫性类型也称为色素沉着绒毛结节性滑膜炎(PVNS)。先前已有42例关于PVNS累及中轴骨骼的报道,其中7例发生于胸椎。本文报道了一名年轻患者,其被发现患有胸椎PVNS,在3周内出现进行性下肢无力和感觉异常。计算机断层扫描和磁共振成像显示T6/7水平有一个后方病变并侵犯局部骨质。该患者接受了肿瘤全切术,术后恢复良好,体征和症状均消失。手术全切是这种疾病的首选治疗方法,术后通过系列影像学检查进行密切随访对于监测局部复发很重要。