224 research outputs found

    Breast Cancer Detection on Automated 3D Ultrasound with Co-localized 3D X-ray.

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    X-ray mammography is the gold standard for detecting breast cancer while B-mode ultrasound is employed as its diagnostic complement. This dissertation aimed at acquiring a high quality, high-resolution 3D automated ultrasound image of the entire breast at current diagnostic frequencies, in the same geometry as mammography and its 3D equivalent, digital breast tomosynthesis, and to extend and help test its utility with co-localization. The first objective of this work was to engineer solutions to overcome some challenges inherent in acquiring complete automated ultrasound of the breast and minimizing patient motion during scans. Automated whole-breast ultrasound that can be registered to X-Ray imaging eliminates the uncertainty associated with hand-held ultrasound. More than 170 subjects were imaged using superior coupling agents tested during the course of this study. At least one radiologist rated the usefulness of X-Ray and ultrasound co-localization as high in the majority of our study cases. The second objective was to accurately register tomosynthesis image volumes of the breast, making the detection of tissue growth and deformation over time a realistic possibility. It was found for the first time to our knowledge that whole breast digital tomosynthesis image volumes can be spatially registered with an error tolerance of 2 mm, which is 10% of the average size of cancers in a screening population. The third and final objective involved the registration and fusion of 3D ultrasound image volumes acquired from opposite sides of the breast in the mammographic geometry, a novel technique that improves the volumetric resolution of high frequency ultrasound but poses unique problems. To improve the accuracy and speed of registration, direction-dependent artifacts should be eliminated. Further, it is necessary to identify other regions, usually at greater depths, that contain little or misleading information. Machine learning, principal component analysis and speckle reducing anisotropic diffusion were tested in this context. We showed that machine learning classifiers can identify regions of corrupted data accurately on a custom breast-mimicking phantom, and also that they can identify specific artifacts in-vivo. Initial registrations of phantom image sets with many regions of artifacts removed provided robust results as compared to the original datasets.Ph.D.Biomedical EngineeringUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.lib.umich.edu/bitstream/2027.42/78947/1/sumedha_1.pd

    A Survey on Deep Learning in Medical Image Analysis

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    Deep learning algorithms, in particular convolutional networks, have rapidly become a methodology of choice for analyzing medical images. This paper reviews the major deep learning concepts pertinent to medical image analysis and summarizes over 300 contributions to the field, most of which appeared in the last year. We survey the use of deep learning for image classification, object detection, segmentation, registration, and other tasks and provide concise overviews of studies per application area. Open challenges and directions for future research are discussed.Comment: Revised survey includes expanded discussion section and reworked introductory section on common deep architectures. Added missed papers from before Feb 1st 201

    Numerical Approaches for Solving the Combined Reconstruction and Registration of Digital Breast Tomosynthesis

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    Heavy demands on the development of medical imaging modalities for breast cancer detection have been witnessed in the last three decades in an attempt to reduce the mortality associated with the disease. Recently, Digital Breast Tomosynthesis (DBT) shows its promising in the early diagnosis when lesions are small. In particular, it offers potential benefits over X-ray mammography - the current modality of choice for breast screening - of increased sensitivity and specificity for comparable X-ray dose, speed, and cost. An important feature of DBT is that it provides a pseudo-3D image of the breast. This is of particular relevance for heterogeneous dense breasts of young women, which can inhibit detection of cancer using conventional mammography. In the same way that it is difficult to see a bird from the edge of the forest, detecting cancer in a conventional 2D mammogram is a challenging task. Three-dimensional DBT, however, enables us to step through the forest, i.e., the breast, reducing the confounding effect of superimposed tissue and so (potentially) increasing the sensitivity and specificity of cancer detection. The workflow in which DBT would be used clinically, involves two key tasks: reconstruction, to generate a 3D image of the breast, and registration, to enable images from different visits to be compared as is routinely performed by radiologists working with conventional mammograms. Conventional approaches proposed in the literature separate these steps, solving each task independently. This can be effective if reconstructing using a complete set of data. However, for ill-posed limited-angle problems such as DBT, estimating the deformation is difficult because of the significant artefacts associated with DBT reconstructions, leading to severe inaccuracies in the registration. The aim of my work is to find and evaluate methods capable of allying these two tasks, which will enhance the performance of each process as a result. Consequently, I prove that the processes of reconstruction and registration of DBT are not independent but reciprocal. This thesis proposes innovative numerical approaches combining reconstruction of a pair of temporal DBT acquisitions with their registration iteratively and simultaneously. To evaluate the performance of my methods I use synthetic images, breast MRI, and DBT simulations with in-vivo breast compressions. I show that, compared to the conventional sequential method, jointly estimating image intensities and transformation parameters gives superior results with respect to both reconstruction fidelity and registration accuracy

    Calibration and Optimization of 3D Digital Breast Tomosynthesis Guided Near Infrared Spectral Tomography

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    Calibration of a three-dimensional multimodal digital breast tomosynthesis (DBT) x-ray and non-fiber based near infrared spectral tomography (NIRST) system is challenging but essential for clinical studies. Phantom imaging results yielded linear contrast recovery of total hemoglobin (HbT) concentration for cylindrical inclusions of 15 mm, 10 mm and 7 mm with a 3.5% decrease in the HbT estimate for each 1 cm increase in inclusion depth. A clinical exam of a patient\u27s breast containing both benign and malignant lesions was successfully imaged, with greater HbT was found in the malignancy relative to the benign abnormality and fibroglandular regions (11 ÎŒM vs. 9.5 ÎŒM). Tools developed improved imaging system characterization and optimization of signal quality, which will ultimately improve patient selection and subsequent clinical trial results

    Automated Deformable Mapping Methods to Relate Corresponding Lesions in 3D X-ray and 3D Ultrasound Breast Images

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    Mammography is the current standard imaging method for detecting breast cancer by using x-rays to produce 2D images of the breast. However, with mammography alone there is difficulty determining whether a lesion is benign or malignant and reduced sensitivity to detecting lesions in dense breasts. Ultrasound imaging used in conjunction with mammography has shown valuable contributions for lesion characterization by differentiating between solid and cystic lesions. Conventional breast ultrasound has high false positive rates; however, it has shown improved abilities to detect lesions in dense breasts. Breast ultrasound is typically performed freehand to produce anterior-to-posterior 2D images in a different geometry (supine) than mammography (upright). This difference in geometries is likely responsible for the finding that at least 10% of the time lesions found in the ultrasound images do not correspond with lesions found in mammograms. To solve this problem additional imaging techniques must be investigated to aid a radiologist in identifying corresponding lesions in the two modalities to ensure early detection of a potential cancer. This dissertation describes and validates automated deformable mapping methods to register and relate corresponding lesions between multi-modality images acquired using 3D mammography (Digital Breast Tomosynthesis (DBT) and dedicated breast Computed Tomography (bCT)) and 3D ultrasound (Automated Breast Ultrasound (ABUS)). The methodology involves the use of finite element modeling and analysis to simulate the differences in compression and breast orientation to better align lesions acquired from images from these modalities. Preliminary studies were performed using several multimodality compressible breast phantoms to determine breast lesion registrations between: i) cranio-caudal (CC) and mediolateral oblique (MLO) DBT views and ABUS, ii) simulated bCT and DBT (CC and MLO views), and iii) simulated bCT and ABUS. Distances between the centers of masses, dCOM, of corresponding lesions were used to assess the deformable mapping method. These phantom studies showed the potential to apply this technique for real breast lesions with mean dCOM registration values as low as 4.9 ± 2.4 mm for DBT (CC view) mapped to ABUS, 9.3 ± 2.8 mm for DBT (MLO view) mapped to ABUS, 4.8 ± 2.4 mm for bCT mapped to ABUS, 5.0 ± 2.2 mm for bCT mapped to DBT (CC view), and 4.7 ± 2.5 mm for bCT mapped to DBT (MLO view). All of the phantom studies showed that using external fiducial markers helped improve the registration capability of the deformable mapping algorithm. An IRB-approved proof-of-concept study was performed with patient volunteers to validate the deformable registration method on 5 patient datasets with a total of up to 7 lesions for DBT (CC and MLO views) to ABUS registration. Resulting dCOM’s using the deformable method showed statistically significant improvements over rigid registration techniques with a mean dCOM of 11.6 ± 5.3 mm for DBT (CC view) mapped to ABUS and a mean dCOM of 12.3 ± 4.8 mm for DBT (MLO view) mapped to ABUS. The present work demonstrates the potential for using deformable registration techniques to relate corresponding lesions in 3D x-ray and 3D ultrasound images. This methodology should improve a radiologists’ characterization of breast lesions which can reduce patient callbacks, misdiagnoses, additional patient dose and unnecessary biopsies. Additionally, this technique can save a radiologist time in navigating 3D image volumes and the one-to-one lesion correspondence between modalities can aid in the early detection of breast malignancies.PHDNuclear Engineering & Radiological SciencesUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttps://deepblue.lib.umich.edu/bitstream/2027.42/150042/1/canngree_1.pd

    QUANTITATIVE THREE DIMENSIONAL ELASTICITY IMAGING

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    Neoplastic tissue is typically highly vascularized, contains abnormal concentrations of extracellular proteins (e.g. collagen, proteoglycans) and has a high interstitial fluid pres- sure compared to most normal tissues. These changes result in an overall stiffening typical of most solid tumors. Elasticity Imaging (EI) is a technique which uses imaging systems to measure relative tissue deformation and thus noninvasively infer its mechanical stiffness. Stiffness is recovered from measured deformation by using an appropriate mathematical model and solving an inverse problem. The integration of EI with existing imaging modal- ities can improve their diagnostic and research capabilities. The aim of this work is to develop and evaluate techniques to image and quantify the mechanical properties of soft tissues in three dimensions (3D). To that end, this thesis presents and validates a method by which three dimensional ultrasound images can be used to image and quantify the shear modulus distribution of tissue mimicking phantoms. This work is presented to motivate and justify the use of this elasticity imaging technique in a clinical breast cancer screening study. The imaging methodologies discussed are intended to improve the specificity of mammography practices in general. During the development of these techniques, several issues concerning the accuracy and uniqueness of the result were elucidated. Two new algorithms for 3D EI are designed and characterized in this thesis. The first provides three dimensional motion estimates from ultrasound images of the deforming ma- terial. The novel features include finite element interpolation of the displacement field, inclusion of prior information and the ability to enforce physical constraints. The roles of regularization, mesh resolution and an incompressibility constraint on the accuracy of the measured deformation is quantified. The estimated signal to noise ratio of the measured displacement fields are approximately 1800, 21 and 41 for the axial, lateral and eleva- tional components, respectively. The second algorithm recovers the shear elastic modulus distribution of the deforming material by efficiently solving the three dimensional inverse problem as an optimization problem. This method utilizes finite element interpolations, the adjoint method to evaluate the gradient and a quasi-Newton BFGS method for optimiza- tion. Its novel features include the use of the adjoint method and TVD regularization with piece-wise constant interpolation. A source of non-uniqueness in this inverse problem is identified theoretically, demonstrated computationally, explained physically and overcome practically. Both algorithms were test on ultrasound data of independently characterized tissue mimicking phantoms. The recovered elastic modulus was in all cases within 35% of the reference elastic contrast. Finally, the preliminary application of these techniques to tomosynthesis images showed the feasiblity of imaging an elastic inclusion.CenSSIS, the Center for Subsurface Sensing and Imaging Systems, under the Engineering Research Centers Program of the National Science Foundation (award number EEC-9986821
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