Garnon Julien, Koch Guillaume, Tsoumakidou Georgia, Caudrelier Jean, Chari Basavaraj, Cazzato Roberto Luigi, Gangi Afshin
Department of Interventional Radiology, Hopitaux universitaires de Strasbourg, 1, Place de l'Hopital, 67096, Strasbourg Cedex, France.
Oxford University Hospitals, Nuffield Orthopaedic Centre, Oxford, UK.
Cardiovasc Intervent Radiol. 2017 Aug;40(8):1267-1273. doi: 10.1007/s00270-017-1638-9. Epub 2017 Mar 29.
To assess the technical feasibility and safety of combined fusion imaging and needle tracking under ultrasound guidance to target bone lesions without cortical disruption.
Between January 2016 and March 2016, seven patients underwent US-guided biopsy of bone lesions without cortical disruption. Targeted bone lesions were measuring more than 1.5 cm with a thin cortex, a trans-osseous pathway not exceeding 2 cm and without any adjacent vulnerable structures. First three procedures were performed in the CT suite to aid the needle tracking where necessary (group 1), the remaining four procedures were performed in the US suite (group 2). In group 1, deviation from the real position of the bone trocar (estimated on CT) was compared to the virtual position (estimated on the fusion CT-US images). In both group, procedure data and histopathological results were collected, and compared to the suspected diagnosis and follow-up.
Mean procedure duration was 44 min. Total number of synchronisation points for combined fusion imaging were 3.3 on average. In group 1, mean deviation between the virtual and real CT coordinates was 5.3 mm on average. All biopsies yielded adequate quality analysable bone sample. Histopathological analysis revealed malignancy in three cases, non-specific inflammation in two cases, and normal bone in two cases. The four benign results were confirmed as true negative results. There were no immediate or post-procedural complications.
The use of combined fusion imaging and needle tracking ultrasound guidance to target bone lesions without cortical disruption seems technically feasible, provided the patient and lesion selection is appropriate.
评估在超声引导下联合融合成像和针追踪技术靶向骨病变且不破坏皮质骨的技术可行性和安全性。
2016年1月至2016年3月期间,7例患者接受了超声引导下未破坏皮质骨的骨病变活检。靶向骨病变直径超过1.5 cm,皮质薄,经骨路径不超过2 cm,且无任何相邻的易损结构。前三例手术在CT室进行,必要时辅助针追踪(第1组),其余四例手术在超声室进行(第2组)。在第1组中,将骨穿刺针实际位置(在CT上估计)与虚拟位置(在融合CT-US图像上估计)的偏差进行比较。在两组中,收集手术数据和组织病理学结果,并与疑似诊断和随访结果进行比较。
平均手术时间为44分钟。联合融合成像的同步点总数平均为3.3个。在第1组中,虚拟和实际CT坐标之间的平均偏差平均为5.3 mm。所有活检均获得了质量足够可分析的骨样本。组织病理学分析显示3例为恶性,2例为非特异性炎症,2例为正常骨。4个良性结果被确认为真阴性结果。无即刻或术后并发症。
如果患者和病变选择合适,使用联合融合成像和针追踪超声引导靶向未破坏皮质骨的骨病变在技术上似乎是可行的。