An exemplary system, method, and computer-accessible medium for detection of structural disorder(s) of patient(s) can be provided which can include, for example, receiving magnetic resonance imaging (MRI) information of the portion(s), generating gadolinium (Gd) enhanced map(s) based on the MRI information using a machine learning procedure(s), and detecting the structural disorder(s) of the patient(s) based on a GD contrast of the Gd enhanced map(s). The Gd enhanced map(s) can be a full dosage Gd enhanced map. The machine learning procedure can be a convolutional neural network. The MRI information can include (i) a low-dosage Gd MRI scan(s), or (ii) a Gd-free MRI scan(s). The Gd contrast can be generated in the Gd enhanced map(s) using a T2-weighted MRI image of the portion(s). Structural disorder(s) can include Stroke, tumor, trauma, infection, Multiple sclerosis and/or other inflammatory disease.

A method of establishing an enhanced three-dimensional (3D) model of intracranial angiography is provided and includes: obtaining a bright-blood image group, a black-blood image group and an enhanced black-blood image group; preprocessing image pairs to obtain first bright-blood images and black-blood images; registering the first bright-blood image by taking the first black-blood image as reference to obtain a registered bright-blood image group; eliminating flowing void artifact to obtain an artifact-elimination enhanced black-blood image group; subtracting each image of the artifact-elimination enhanced black-blood image group from corresponding black-blood image to obtain angiography enhanced images; establishing a blood 3D model and a vascular 3D model with blood boundary expansion by using the registered bright-blood image group; establishing an angiography enhanced 3D model by using the angiography enhanced images; obtaining an enhanced 3D model of intracranial angiography based on the blood 3D model, the vascular 3D model and the angiography enhanced 3D model.

The invention provides for a method of training a neural network (322) configured for providing a further processing location (326). The method comprises providing (200) a labeled medical image (100), wherein the labeled medical image comprises multiple labels each indicating a truth processing location (102, 104, 106). The method further comprises inputting (202) the labeled medical image into the neural network to obtain one trial processing location. The one trial processing location comprises a most likely trial processing location (108). The method further comprises determine (204) the closest truth processing location (106) for the most likely trial processing location. The method further comprises calculating (206) an error vector (110) using the closest truth processing location and the most likely trial processing location. The method further comprises training (208) the neural network using the error vector.

A medical navigation system is provided for registering a patient for a medical procedure with the medical navigation system using fiducial markers. The fiducial markers are placed on the patient prior to a 3D scan and the fiducial markers each have a target for use with a tracking system. The medical navigation system comprises a 3D scanner, a tracking system, a display, and a controller electrically coupled to the 3D scanner, the tracking system, and the display. The controller has a processor coupled to a memory. The controller is configured to: receive 3D scan data generated by the 3D scanner representative of a 3D scan of at least a portion of the patient, the 3D scan including the fiducial markers visible by the 3D scanner; load from the memory saved medical image data, the saved medical data including preoperative image data saved during a previous scan of at least a portion of the patient; receive position data from the tracking system based on the target for each of the fiducial markers; and perform a transformation mapping to create a single unified virtual coordinate space based on the 3D scan data, the position data, and the medical image data, and updating registration data of the medical navigation system based on the transformation mapping.

The present disclosure relates to systems and methods for determining quantitative chemical exchange or exchangeable proton information from a region-of-interest in a subject. The methods and systems use adaptive fitting to quantify magnetic resonance (MR) data, such as chemical exchange saturation transfer magnetic resonance imaging (CEST MRI) images, using initial values based on, for example, Lorentzian fitting. Images are iteratively less downsampled until quantitative maps of desired resolution are obtained. Such an approach allows for reliable fitting at a faster fitting speed, and is less susceptible to suboptimal signal to noise (SNR) than conventional methods.

In a method and processor for evaluating a contrast agent-enhanced two-dimensional magnetic resonance slice image of a heart of a patient in order to determine picture elements revealing contrast agent deposits in the myocardium, an endocardium contour in the magnetic resonance slice image, taking into consideration deposition information describing picture elements potentially revealing contrast agent deposits and determined by image analysis on the basis of a shape assumption for the heart structure that is to be examined, in particular the left ventricle, such that picture elements potentially revealing contrast agent deposits are avoided as much as possible as a contour component. An epicardium contour enclosing the endocardium contour is then determined. Picture elements are marked that indicate contrast agent enhancement in the myocardium lying between the epicardium contour and the endocardium contour as contrast agent deposit.

Methods, apparatus, and other embodiments associated with classifying a region of tissue using quantified vessel tortuosity are described. One example apparatus includes an image acquisition logic that acquires an image of a region of tissue demonstrating cancerous pathology, a delineation logic that distinguishes nodule tissue within the image from the background of the image, a perinodular zone logic that defines a perinodular zone based on the nodule, a feature extraction logic that extracts a set of features from the image including a set of tortuosity features, a probability logic that computes a probability that the nodule is benign, and a classification logic that classifies the nodule tissue based, at least in part, on the set of features or the probability. A prognosis or treatment plan may be provided based on the classification of the image.

A method and apparatus for automated prostate tumor detection and classification in multi-parametric magnetic resonance imaging (MRI) is disclosed. A multi-parametric MRI image set of a patient, including a plurality of different types of MRI images, is received. Simultaneous detection and classification of prostate tumors in the multi-parametric MRI image set of the patient are performed using a trained multi-channel image-to-image convolutional encoder-decoder that inputs multiple MRI images of the multi-parametric MRI image set of the patient and includes a plurality of output channels corresponding to a plurality of different tumor classes. For each output channel, the trained image-to image convolutional encoder-decoder generates a respective response map that provides detected locations of prostate tumors of the corresponding tumor class in the multi-parametric MRI image set of the patient.

A data processing method for determining an enhancing structure of interest within an anatomical body part, wherein the structure of interest exhibits an enhanced signal in an image of the anatomical body part generated by a medical imaging method using a contrast agent, said method being designed to be performed by a computer and comprising a region growing algorithm.

Methods, apparatus, and other embodiments distinguish disease phenotypes and mutational status using co-occurrence of local anisotropic gradient orientations (CoLIAGe) and Laws features. One example apparatus includes a set of circuits that acquires a radiologic image (e.g., MRI image) of a region of tissue demonstrating breast cancer, computes a gradient orientation for a pixel in the MRI image, computes a significant orientation for the pixel based on the gradient orientation, constructs a feature vector that captures a discretized entropy distribution for the image based on the significant orientation, extracts a set of texture features from the MRI image, and classifies the phenotype of the breast cancer based on the feature vector and the set of texture features. Embodiments of example apparatus may generate and display a heatmap of entropy values for the image. Example methods and apparatus may operate substantially in real-time, or may operate in two, three, or more dimensions.