Qscan Radiology Clinics, Kingston, Australian Capital Territory, Australia.
J Med Imaging Radiat Oncol. 2022 Sep;66(6):738-748. doi: 10.1111/1754-9485.13352. Epub 2021 Nov 26.
This retrospective study aimed to determine the percentage of MRI-detected breast cancers diagnosed using targeted ultrasound and standard 14-gauge (14g) biopsy in the setting of an Australian breast MRI service. This is of clinical relevance because malignancies not identifiable on mammography or by ultrasound may then require more invasive, technically demanding and costly MRI-guided interventional procedures, usually by large-core vacuum-assisted biopsy (VAB) or hook-wire localisation with open surgical biopsy.
On review of the 12-year period 2006-2018, we identified 67 new breast cancer events in 64 women where the diagnosis was made on the basis of the MRI scan findings either alone (n = 60) or in combination with a concurrent mammogram (n = 7), with no recorded clinical abnormality. The percentage in which malignancy was confirmed on histopathology using targeted ultrasound in combination with 14g biopsy was determined versus other biopsy methods, for both invasive cancer and in situ disease.
Ultrasound-guided 14g biopsy was successful in establishing the presence of malignancy in 42/46 (91%) of events with a final diagnosis of invasive cancer, with 2 more proven by MRI-guided interventional procedures (1 VAB and 1 hook-wire) and 1 by open surgical biopsy. In the final case, a 5 mm focus on MRI with no sonographic correlate at the initial presentation was only identified and biopsied by ultrasound at 12-month follow-up. For events with a final diagnosis of DCIS/pLCIS (pleomorphic LCIS, n = 2), US-guided 14g biopsy was successful in 10/21 (48%), while 4/7 events with corresponding mammographic microcalcifications were proven by x-ray stereotactic interventions. A further 5 events had MRI-guided interventions (3 VAB and 2 hook-wires) and 1 an open surgical biopsy to confirm malignancy. In the final case (a woman with a 30 × 20 mm focal area of non-mass enhancement with corresponding microcalcifications consistent with DCIS), a pathologic diagnosis was not made until the patient presented 5 years later with invasive disease. There were also 3 instances of upgrades to invasion on final surgical pathology, one from pLCIS to microinvasion and 2 others from DCIS to IDC. Among the DCIS/pLCIS events, semi-random 14g core biopsy (sampling at the expected location of the MRI abnormality without a specific sonographic correlate) proved to be successful in 3 women.
Ultrasound-guided 14g core biopsy established a malignant diagnosis in 91% of invasive cancers and in 48% of DCIS/pLCIS cases. This relatively non-invasive, technically easy to perform and low-cost biopsy procedure can be used immediately when targeted ultrasound shows a correlate for a suspicious MRI scan finding. Careful imaging-pathologic correlation is required after 14g biopsy, and a discordant result will usually prompt recourse to an MRI-guided VAB or hook-wire localisation.
本回顾性研究旨在确定在澳大利亚乳腺 MRI 服务中,通过靶向超声和标准 14 号(14g)活检诊断的 MRI 检测乳腺癌的百分比。这具有临床相关性,因为在乳腺 X 线摄影或超声检查中无法识别的恶性肿瘤可能需要更具侵袭性、技术要求更高且成本更高的 MRI 引导介入程序,通常采用大芯真空辅助活检(VAB)或钩wire 定位联合开放式外科活检。
在回顾 2006-2018 年的 12 年期间,我们在 64 名女性中发现了 67 例新的乳腺癌事件,这些女性的诊断是基于 MRI 扫描结果得出的,要么单独(n=60),要么与同时进行的乳腺 X 线摄影结果相结合(n=7),且无记录的临床异常。确定了在有或无同时进行的乳腺 X 线摄影的情况下,通过靶向超声联合 14g 活检证实恶性肿瘤的百分比,用于确定浸润性癌症和原位疾病的其他活检方法。
超声引导的 14g 活检成功确定了 46 例最终诊断为浸润性癌症的事件中恶性肿瘤的存在,其中 2 例通过 MRI 引导的介入程序(1 例 VAB 和 1 例钩wire)和 1 例通过开放式外科活检证实。在最后一个病例中,MRI 上显示的 5mm 焦点在初始表现时没有超声相关性,仅在 12 个月的随访时通过超声检查发现并活检。对于最终诊断为 DCIS/pLCIS(多形性 LCIS,n=21)的事件,US 引导的 14g 活检成功确定了 10/21(48%),而在 7 例有相应乳腺微钙化的事件中,X 射线立体定向干预证实了恶性肿瘤的存在。进一步的 5 例事件进行了 MRI 引导的介入(3 例 VAB 和 2 例 hook-wire),1 例进行了开放式外科活检以确认恶性肿瘤。在最后一个病例(一名女性,30×20mm 局灶性非肿块增强,伴有与 DCIS 一致的微钙化),直到 5 年后患者出现浸润性疾病时才做出病理诊断。最终手术病理还有 3 例升级为浸润性,其中 1 例从 pLCIS 升级为微浸润,另外 2 例从 DCIS 升级为 IDC。在 DCIS/pLCIS 事件中,半随机的 14g 核心活检(在 MRI 异常的预期位置进行采样,而没有特定的超声相关性)在 3 名女性中成功确定了恶性肿瘤。
超声引导的 14g 核心活检在 91%的浸润性癌症和 48%的 DCIS/pLCIS 病例中确定了恶性诊断。这种相对非侵入性、技术上易于执行且成本较低的活检程序可以在靶向超声显示可疑 MRI 扫描结果的相关性时立即使用。在进行 14g 活检后需要仔细进行影像学与病理学的相关性评估,如果结果不一致,通常需要进行 MRI 引导的 VAB 或 hook-wire 定位。