Toshiba Medical Systems Corporation

Canon Medical Systems Corporation

Xiangzhi Zhou

Mitsue Miyazaki

Tsutomu Hoshino

Cheng Ouyang

Aiming Lu

Yoshimori Kassai

Satoshi Sugiura

Devices and methods are provided for analyzing images from a magnetic resonance (MR) system. The device includes at least one hardware processor coupled with a storage system accessible to the at least one hardware processor. The device further includes a display in communication with the at least one hardware processor. The device receives a plurality of non-contrast MR images in a region of interest (ROI). The device obtains blood flow signals from the plurality of non-contrast MR images. The device identifies an abnormal segment by analyzing the blood flow signals. The device displays the non-contrast MR images by a highlighted segment in at least one of the non-contrast MR images to indicate the abnormal segment on the display.

System and method for non-contrast myocardium diagnosis support

A magnetic resonance imaging apparatus according to an embodiment includes sequence control circuitry and processing circuitry. The sequence control circuitry executes a first pulse sequence and a second pulse sequence, the first pulse sequence including a first spoiler pulse serving as a dephasing gradient pulse of a first amount, the second pulse sequence including a second spoiler pulse serving as a dephasing gradient pulse of a second amount being different from the first amount or the second pulse sequence not including a spoiler pulse serving as a dephasing gradient pulse. The processing circuitry performs a subtraction operation between a first data obtained from the first pulse sequence and a second data obtained from the second pulse sequence, thereby generating an image.

Magnetic resonance imaging apparatus and magnetic resonance imaging method

A magnetic resonance imaging apparatus according to an embodiment includes sequence control circuitry and processing circuitry. The sequence control circuitry performs first data acquisition in a full k-space and performs a plurality of second data acquisition in partial k-spaces, each of the partial k-spaces being smaller than the entirety of the full k-space. The processing circuitry generates an image, based on data acquired from the first data acquisition and a plurality of pieces of data acquired from the plurality of second data acquisition.

A magnetic resonance imaging apparatus according to an embodiment includes sequence control circuitry. The sequence control circuitry applies an MT (Magnetization Transfer) pulse over a plurality of slices under a gradient magnetic field and configured to apply, for each of the plurality of slices to which the MT pulse is applied, an RF pulse having a frequency corresponding to a resonance frequency of certain protons in each of the plurality of slices.

A magnetic resonance imaging method executed in a magnetic resonance imaging apparatus according to an embodiment comprises: applying an inversion pulse; executing a subsequent imaging sequence including an RF (Radio Frequency) pulse and a gradient magnetic field concurrently applied with the RF pulse in a slice direction and performing, for a slice position selected by the RF pulse and the gradient magnetic field and during a time period including a null point, data acquisition in a plurality of orientations including a center of a two-dimensional k-space.

Magnetic resonance imaging method

Black blood time to inversion (BBTI) tag-on and tag-off images acquired by magnetic resonance imaging (MRI) are analyzed to produce difference magnitude 3D images as a function of time (BBTI values) representing blood perfusion in a region of interest (ROI). Perfusion data of the ROI having values which are different for normal and abnormal myocardial tissues are displayed for plural slices of a 3D image and for plural BBTI values in a single display panel.

Non-contrast dynamic MRI myocardial perfusion analysis and visualization

A magnetic resonance imaging apparatus includes a sequence controller. The sequence controller is configured to apply MT (Magnetization Transfer) pulses having a frequency different from a resonance frequency of free water protons and then acquires magnetic resonance signals of an object to be imaged. The sequence controller acquires the magnetic resonance signals for each of multiple frequencies while changing the frequency of MT pulses within a frequency band based on a T2 relaxation time of restricted protons contained in the object to be imaged.

Magnetic resonance imaging apparatus

A magnetic resonance imaging apparatus according to an embodiment includes control circuitry and processing circuitry. The control circuitry executes a first pulse sequence performing MR (Magnetic Resonance) spectroscopy and configured to execute a second pulse sequence applying an MT (Magnetization Transfer) pulse. The processing circuitry causes a display to present first data acquired based on the first pulse sequence and second data acquired based on the second pulse sequence.

A magnetic resonance imaging (MRI) system, method and/or computer readable medium is configured reduce specific absorption rate (SAR) in Fast Advanced Spin Echo (FASE) or Single-shot Fast Spin Echo (SS-FSE) imaging used, for example, in non-contrast magnetic resonance angiography (NC-MRA) techniques like fresh blood imaging (FBI). Within RF pulse sequences used to acquire echo data, the refocusing flip angles may be varied in the phase encode direction, and/slice encode direction, such that the refocusing pulse (or pulses) that map echo signals to the k-space center region larger refocusing flip angles than refocusing pulses used to generate echo signals that map to other areas of k-space. In some instances, the TR interval also may be varied for RF pulse sequences such that central K-space have a longer TR than the slices further towards the ends.

SAR reduction in fast advanced spin echo (FASE) or single-shot fast spin echo (SS-FSE) imaging

Chemical exchange saturation transfer (CEST) effects are enhanced by forming, for each of a plurality of magnetization transfer (MT) offset frequencies within a specified first range, a respective image representing CEST effects. A subset of the formed CEST images is displayed and a preferred or optimum one is selected from a display screen. The thus identified target frequency is then used to generate a composite enhanced CEST image based upon a combination of formed CEST images having MT frequencies within a specified second, smaller range, around the identified target frequency.

Systems, methods and GUI for chemical exchange saturation transfer (CEST) analysis

A magnetic resonance imaging (MRI) system, method and/or computer readable medium is configured to obtain bright signal while having acceptable specific absorption rate (SAR) and acceptable scan time in Fast Advanced Spin Echo (FASE) or Single-shot Fast Spin Echo (SS-FSE) imaging used, for example, in non-contrast magnetic resonance angiography (NC-MRA) techniques like fresh blood imaging (FBI). Within RF pulse sequences used to acquire echo data, the TR intervals are varied in the slice encode direction. In some instances, the refocusing pulse flip angles too may be varied for RF pulse sequences such that central k-space have larger refocusing pulse flip angles than slices further towards the ends.

Variable TR (vTR) function in fresh blood imaging (FBI)

MRI k-space data is acquired for a patient ROI during data acquisition sequences including a nuclear magnetic resonance (NMR) signal readout period using a late gadolinium enhanced (LGE) data acquisition sequence including at least one fat-specific RF NMR magnetization inversion pulse imposed (a) after a water-specific RF NMR magnetization inversion pulse timed to cause a substantial null in NMR magnetization of normal tissue protons near a center of the readout period and (b) before the readout period center, which fat-specific inversion pulse is also timed to cause a substantial null in NMR magnetization of fat tissue protons near the readout period center. The acquired MR image data is reconstructed into a contrast enhanced LGE image of tissues within the ROI but having substantially suppressed normal and fat components therein.

Enhanced fat saturation in myocardial infarction MRI

A magnetic resonance imaging (MRI) system, method and/or computer readable storage medium is configured to effect enhanced magnetic transfer (MT) effects and chemical exchange saturation transfer (CEST) effects. The configured techniques include irradiating an object in an MRI gantry by applying a sequence of magnetic transfer (MT) pulses over a range of different frequencies, and then applying an MR imaging sequence to the irradiated object.

Enhancement of MT effect and/or CEST effect

Elicited MRI signals are processed into MR image data in conjunction (a) with use of an initial spatially-selective RF tag pulse (tag-on) and (b) without use of an initial spatially-selective NMR RF tag pulse (tag-off) in respectively corresponding data acquisition subsequences. Multi-dimensional tag-on and tag-off data acquisition subsequences are used for each of plural time-to-inversion (TI) intervals without using an injected contrast agent. Acquired image data sets are subtracted for each TI interval to produce difference values as a function of time representing blood perfusion for the ROI that differentiates between normal, ischemic and infarct tissues.

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Vernon Hills, IL, United States of America

Xiangzhi Zhou