Zeng Piaoe, Zhang Annan, Song Le, Liu Jianfang, Yuan Huishu, Zhang Weifang
Department of Radiology, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Department of Nuclear Medicine, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Insights Imaging. 2021 Jul 13;12(1):98. doi: 10.1186/s13244-021-01025-2.
To review the clinical and imaging data of spinal giant cell tumour of the tendon sheath (GCTTS) to improve our understanding of the disease.
The imaging findings, clinicopathological features and clinical outcomes of 14 patients with pathologically confirmed spinal GCTTS were analysed retrospectively.
All 14 patients had a single spinal lesion, including ten cervical vertebra lesions and four thoracic vertebra lesions. CT scan findings: The lesions showed osteolytic bone destruction and were centred on the facet joint, eroding the surrounding bone with a paravertebral soft tissue mass. MRI scan findings: all the lesions manifested predominantly as isointense or hypointense on T1-weighted imaging (T1WI). On T2-weighted imaging (T2WI), eight lesions were hypointense, and four were isointense. The remaining two lesions showed slight hyperintensity. The enhanced scans of eight lesions showed moderate to marked homogeneous or heterogeneous enhancement. PET/CT findings: Among the five patients who underwent PET/CT, three presented lesions with well-defined, sclerotic borders, and the uptake of F-FDG was markedly increased. One lesion showed an ill-defined border and an uneven increase in F-FDG uptake with an SUVmax value of 8.9. A recurrent lesion was only found on PET/CT 45 months after surgery and the SUVmax was 5.1.
Spinal GCTTS is extremely rare. Osteolytic bone destruction in the area of the facet joint with a soft tissue mass and hypointensity on T2WI images are indicative of the spinal GCTTS. GCTTS shows high uptake of F-FDG, and PET/CT is helpful in detecting recurrent lesions.
回顾腱鞘巨细胞瘤(GCTTS)累及脊柱的临床及影像学资料,以提高对该疾病的认识。
回顾性分析14例经病理证实的脊柱GCTTS患者的影像学表现、临床病理特征及临床结局。
14例患者均为单发性脊柱病变,其中颈椎病变10例,胸椎病变4例。CT扫描表现:病变呈溶骨性骨质破坏,以小关节为中心,侵蚀周围骨质并伴有椎旁软组织肿块。MRI扫描表现:所有病变在T1加权像(T1WI)上主要表现为等信号或低信号。在T2加权像(T2WI)上,8个病变呈低信号,4个呈等信号,其余2个病变呈轻度高信号。8个病变的增强扫描表现为中度至明显的均匀或不均匀强化。PET/CT表现:5例行PET/CT检查的患者中,3例病变边界清晰、有硬化边,F-FDG摄取明显增加。1例病变边界不清,F-FDG摄取不均匀增加,SUVmax值为8.9。1例复发病变仅在术后45个月的PET/CT检查中发现,SUVmax为5.1。
脊柱GCTTS极为罕见。小关节区域的溶骨性骨质破坏伴软组织肿块及T2WI图像上的低信号是脊柱GCTTS的特征性表现。GCTTS显示F-FDG摄取较高,PET/CT有助于检测复发病变。