Department of Radiology, Otto von Guericke University, Medical School, Leipziger Strasse 44, 39120 Magdeburg, Germany.
Radiology. 2012 Nov;265(2):359-70. doi: 10.1148/radiol.12110981. Epub 2012 Aug 24.
To identify the most appropriate magnetic resonance (MR) sequence for breast biopsy with regard to lesion visibility and artifact size and to assess feasibility and safety of this approach in a clinical setting.
MR-guided interventions were performed in an open 1.0-T MR imager between November 2009 and January 2011. The prospective clinical study was approved by the institutional review board. Written informed consent was obtained. Four different fast dynamic sequences (balanced steady-state free precession, T1-weighted turbo gradient-echo, T1-weighted turbo spin-echo [SE], and T2-weighted single-shot SE sequences) were evaluated for artifact size of biopsy needle and in vivo for lesion visibility. In vivo breast biopsies were performed with the freehand technique and without immobilization or a positioning device by using an interactive MR mode that allowed continuous imaging in two orthogonal planes for guidance.
On the basis of good lesion detection in combination with small artifact size, T1-weighted SE imaging was used for biopsy. A total of 75 biopsies were performed successfully in 69 patients (mean age, 53 years; age range, 35-78 years) (mean lesion size, 7.1 mm; range, 4-15 mm). The interactive MR platform enabled immediate localization and correction of intended needle trajectory. Average time for freehand biopsy was 12 minutes (range, 8-23 minutes). No major complications were recorded.
MR-guided freehand biopsy of breast lesions with the near-real-time interactive MR platform in an open 1.0-T MR imager is safe and feasible in a clinical setting. The method simplifies work flow and intervention performance.
确定在显示病灶和伪影大小方面最适合乳腺活检的磁共振(MR)序列,并评估该方法在临床环境中的可行性和安全性。
2009 年 11 月至 2011 年 1 月,在开放式 1.0-T MR 成像仪中进行了 MR 引导介入。该前瞻性临床研究获得了机构审查委员会的批准。获得了书面知情同意书。评估了 4 种不同的快速动态序列(平衡稳态自由进动、T1 加权涡轮梯度回波、T1 加权涡轮自旋回波[T1-W SE]和 T2 加权单次激发 SE 序列)的活检针伪影大小,并在体内评估了病灶显示情况。采用徒手技术,在没有固定或定位装置的情况下,在允许在两个正交平面连续成像的交互 MR 模式下进行了体内乳腺活检。
根据良好的病灶检出率和较小的伪影大小,选择 T1-W SE 成像用于活检。在 69 例患者(平均年龄 53 岁;年龄范围,35-78 岁)中成功进行了总共 75 例活检(平均病灶大小 7.1mm;范围,4-15mm)。交互 MR 平台能够立即定位和校正预期的针道。徒手活检的平均时间为 12 分钟(范围,8-23 分钟)。未记录到主要并发症。
在开放式 1.0-T MR 成像仪中使用近实时交互 MR 平台进行的 MR 引导徒手乳腺病变活检在临床环境中是安全且可行的。该方法简化了工作流程和介入操作。