Tips for finding magnetic resonance imaging-detected suspicious breast lesions using second-look ultrasonography: a pictorial essay
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Abstract
Second-look ultrasonography (US) is a targeted breast US examination that evaluates suspicious lesions detected on magnetic resonance imaging (MRI). It is a useful tool for determining the probability of malignancy and facilitating US-guided biopsy. Lesions detected on MRI and US should be correlated accurately, which is challenging in some cases. This article documents second-look US and MRI findings that are correlated with the pathology, and suggests helpful approaches for correlating between the two modalities.
Introduction
Breast magnetic resonance imaging (MRI) is the most sensitive modality for detecting and staging breast cancer [1,2]. However, its specificity is limited, and it is difficult to manage when there are multiple suspicious lesions [3]. Additional MRI-detected suspicious breast lesions in patients with breast cancer have a higher probability of malignancy than those in patients without breast cancer [4]. Second-look or targeted ultrasonography (US) helps to evaluate suspicious lesions that have been detected on MRI. It is a useful diagnostic tool for determining the probability of malignancy, and it also facilitates biopsy or pre-surgical wire-localization [5]. However, an accurate lesion diagnosis requires correlation between MRI and US findings [6]. The surgical plan may be changed according to the pathologic results of an additional MRI-detected lesion [4]. This article aimed to document second-look US and MRI findings that are correlated with the pathology and to suggest helpful approaches for correlating between the two modalities.
The Clinical Needs and Limitations of Second-Look US
Breast MRI determines the local tumor extent, multifocality, multicentricity, or bilaterality of breast cancer with higher accuracy than mammography or US [1]. MRI depicts additional malignant lesions that are not discerned by other imaging techniques in up to 37% of patients [2]. Since international recommendations for breast MRI have been published, preoperative staging with MRI has been widely used in patients with breast cancer [7]. Because of the increasing application of MRI in clinical practice, the detection of additional suspicious lesions is also increasing [7]. This has been accompanied by a greater need for histologic confirmation preoperatively [8]. However, MRI-guided biopsy is time-consuming, expensive, and requires special equipment. In this context, second-look US is a cost-effective tool to evaluate suspicious MRI-detected lesions that facilitates US-guided biopsy and pre-surgical wire-localization [5,6].
The detection rate of additional suspicious lesions with second-look US varies from 23% to 89% [6,7]. This high variability can be attributed to the lesion type (mass vs. non-mass) and final lesion diagnosis (malignant vs. benign) [7]. Previous studies have reported that US correlation for MRI-detected lesions was more likely for masses than for non-mass enhancement [7-9], because additional MRI-detected lesions are often small and sonographically subtle, especially in cases of non-mass enhancement [10].
Malignant lesions are more likely to be identified on second-look US than benign lesions [7,9,10]. However, a negative second-look US does not exclude malignancy [7]. Previous studies reported that 10%-20% of additional MRI-detected lesions that were not visible on US were malignant [7]. In cases where suspicious lesions are not visible on US, MRI-guided biopsy should be considered.
When US-guided biopsy is performed, the concordance between the imaging findings and pathologic results should be reviewed. MRI-guided biopsy or surgical excision should be considered if a discordant result is obtained. A follow-up examination is required even if the results are concordant benign, because approximately 14% of lesions that underwent US-guided biopsy did not correspond to an MRI-detected lesion, and 29% of them were diagnosed as malignant at re-biopsy [4,7]. In addition, the operator’s experience and differences in technical equipment can impact the detection rate of second-look US. It is important to improve the accuracy of second-look US through careful scanning and correlation.
Tips to Find Additional MRI-Detected Suspicious Lesions Using Second-Look US
Location of the Lesion
To localize and identify the MRI-detected suspicious lesion via second-look US, a clockwise direction is preferable, and the distance from the nipple should be considered (Fig. 1) [11]. Breast MRI is commonly performed with the patient in the prone position, whereas the breast US is performed with the patient in the supine or supine oblique position. In the supine position, all tissue layers are flattened, especially fatty tissue, which is more compressible than other breast structures. In the prone position, the breasts are pendant and less compressed [4,6]. When performing second-look US, it is important to understand that spatial displacement of the lesion may occur due to body positioning differences [12,13]. This frequently occurs in breasts with a greater amount of fatty tissue, and this could cause considerable variability in the apparent lesion position [12]. Thus, the scanning range of second-look US should be extended to the quadrants, where MRI lesions are expected to move [12,13].
A lesion located in the subareolar area may be missed due to the nipple shadow. These lesions can be visualized better by pushing the nipple upward with the US probe to remove or reduce posterior shadowing due to the nipple (Fig. 2) [4,14].
Depth of the Lesion
When correlating MRI and US findings, the lesion depth with respect to the mammary parenchymal zone and its proximity to the anterior and posterior mammary fascia should be considered [12,15]. On US, the mammary fascia appears as thin echogenic lines, encompassing the mammary parenchymal zone. These serve as landmarks to evaluate lesion depth relative to the breast tissue [16]. Based on MRI, the lesion should be localized according to the premammary, mammary, and retromammary zones [16]. Although the lesion depth is not identical between the two modalities, the corresponding mammary zone remains constant [4]. It is possible to predict the depth of the lesion when only the glandular tissue is considered (Fig. 3). All breast tissue layers, especially fatty tissue, are flattened on US. As the retromammary fat is markedly thinned on US, lesions that abut the posterior mammary fascia are more posteriorly located on US than on MRI (Fig. 4).
Size and Shape of the Lesion
The size and shape of the lesion can be used to detect the target lesion on US. However, the size and shape of the lesion are not always identical between US and MRI, especially for non-mass enhancements [17]. The lesions appear smaller and flatter on US because of the supine positioning of the patient and vertical compression by the US probe (Fig. 5). Associated findings of the lesion, such as ductal extension, are also helpful for correlation between the two modalities [4].
Landmarks
Anatomical breast structures (e.g., vessels, fat lobule distribution, Cooper’s ligament) near the targeted lesion are viable landmarks to detect the lesion on US and correlate between the two modalities. Izumori et al. [14] reported a high identification rate (99%) using anatomical structures as indicators. Specific features of the morphology of the surrounding tissue will help correlate the two modalities (Fig. 6). Coexisting lesions (e.g., known breast cancer, known fibroadenoma, cyst, scar, implant) are also helpful identifiers for the lesion [4,6]. These landmarks should be carefully reviewed on T2-weighted and pre-contrast T1-weighted images, because anatomical structures are well visualized on these images. It is noteworthy that the distance between two lesions varies between the two modalities according to the amount of fatty tissue in the breast (Fig. 7).
Complementary US Techniques
Several complementary techniques have been used to detect target lesions on second-look US. Color or power Doppler imaging helps identify the internal vascularity of a solid mass. Malignant lesions have increased blood flow on Doppler imaging, which suggests neoangiogenesis. This finding is consistent with the mechanism of contrast enhancement on MRI (Fig. 8). Elastography is a complementary technique that reflects the hardness of the lesion. Malignant lesions are typically harder than the surrounding tissue. Elastography is useful for distinguishing true lesions when the US findings are subtle (Fig. 9) [16]. Tissue harmonic imaging improves image contrast and lateral resolution by providing a clearer definition of the lesion margins. Therefore, tissue harmonic imaging identifies subtle isoechoic lesions by revealing hypoechoic lesions to differentiate them from the surrounding fatty tissue (Fig. 10) [18].
Conclusion
When performing second-look US, it is essential to understand the differences between US and MRI in terms of basic principles and breast position. To accurately identify MRI-detected suspicious lesions on second-look US, the lesion location, depth, and size/shape must be considered. Anatomical structures and coexisting lesions can be useful indicators, and complementary US techniques are helpful for identifying subtle breast lesions. Detecting lesions and correlating the findings between MRI and US are important to prevent unnecessary biopsies or delayed diagnoses.
Notes
Author Contributions
Conceptualization: Lee SE, Kim YS. Data acquisition: Jeon T, Lee SE, Kim YS, Son HM. Data analysis or interpretation: Jeon T, Son HM. Drafting of the manuscript: Jeon T. Critical revision of the manuscript: Lee SE, Kim YS, Son HM. Approval of the final version of the manuscript: all authors.
No potential conflict of interest relevant to this article was reported.
Acknowledgements
This study was supported by a research grant from Yeungnam University.
References
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Notes
Key point
Second-look ultrasound (US) is a useful tool for determining the probability of a malignancy and facilitating US-guided biopsy. Lesions detected on magnetic resonance imaging (MRI) and US should be correlated accurately, which is challenging in some cases. This article documented the second-look US and MRI findings, which were correlated with the pathology, and suggested helpful approaches for correlating between the two modalities.