A system for controlling operation of an imaging or therapy apparatus. The system comprises an interface (IN) for receiving a pain measurement signal as measured by one or more sensors (S) in relation to an anatomic part (BR) of the patient (PAT) i) being imaged in an imaging procedure by the imaging apparatus or ii) being under therapy in a therapy procedure delivered by the therapy device, whilst the part (BR) is held in an adjustable fixation device (FD). A control unit (CU) of the system is configured to process the pain measurement signal to compute at least one control signal. A control interface (CIF) of the system is configured to interact during the imaging or therapy procedure with the imaging apparatus (IA) and/or the fixation device (FD) based on the control signal to a) influence the imaging or therapy procedure and/or b) to adjust the fixation device so as to change the manner in which the part (BR) is being held.

Described herein are paddles for breast biopsies. A reverse paddle and a compression paddle may be used in a breast biopsy. Both paddles may each have an aperture. When pressed against the breast, the reverse paddle and the compression paddle may allow the breast to bulge out of the aperture of both paddles during the biopsy. As the breast tissue bulges out of both paddles, the breast tissue to be examined via biopsy may be enlarged, thereby lessening the use of excisional biopsies on subjects with thin breasts.

Processes and techniques are disclosed to identify regions of suspected malignancy and their localization within a body part or organ. These methods rely on the analysis of infrared images to identify thermal abnormalities using image post-processing techniques, numerical modeling, iterative solutions methodology or a digital library. The methods utilize noninvasive, non-radiative and no contact infrared imaging that can be used for breast cancer screening for improved prognosis.

A medical imaging system comprising: a microwave antenna array comprising a transmitting antenna and a plurality of receiving antennae, wherein the transmitting antenna is configured to transmit microwave signals so as to illuminate a body part of a patient and the receiving antennae are configured to receive the microwave signals following scattering within the body part; a processor configured to process the scattered microwave signals and generate an output indicative of the internal structure of the body part to identify a target within the body part; and an ablation probe comprising an ablation needle movable relative to the microwave antenna array; wherein the receiving antennae are further configured to receive microwave signals scattered or emitted by the ablation needle and the processor is further configured to monitor a position of the ablation needle and to guide the ablation needle to the identified target within the body part which it can be used to perform an ablation procedure.

Devices and methods for obtaining external shapes and internal tissue geometries, as well as tissue behaviors, of a biological body segment are provided. A device for three-dimensional imaging of a biological body segment includes a structure configured to receive the biological body segment, the structure including a first array of imaging devices disposed about a perimeter of the device to capture side images of the biological body segment and a second array of imaging devices disposed at an end of the device to capture images of a distal portion of the biological body segment. The second array has a generally axial viewing angle relative to the perimeter. A controller is configured to generate a three-dimensional reconstruction of the biological body segment based on cross-correlation of captured images from the first and second arrays.

There is disclosed a patient table for NMR mammography comprising a test subject for and two openings with are intended for inserting a breast in each case, coils being present in the immediate vicinity thereof, characterised in that in the region of an opening, below the table, a band (3) is attached, which is guided medially inwardly from the outside of the table or of the test subject, here surrounds the breast cranially or caudally, and then runs from the medial side, bearing against the breast for caudal or cranial contact with the breast, the ends of the band (13) being guided laterally outwardly, where they run adjacent to one another.

Processes and techniques are disclosed to identify regions of suspected malignancy and their localization within a body part or organ. These methods rely on the analysis of infrared images to identify thermal abnormalities using image post-processing techniques, numerical modeling, iterative solutions methodology or a digital library. The methods utilize noninvasive, non-radiative and no contact infrared imaging that can be used for breast cancer screening for improved prognosis.

A method for optimizing an X-ray imaging system during a mammographic examination. In order to provide an optimization of the X-ray imaging a breast is compressed between a support plate and a compression plate. A force-height curve is then acquired during the compression. An elasticity value of the breast is determined based on the force-height curve. A parameter of the X-ray imaging system is optimized based on the determined elasticity value.

To provide a photoacoustic probe capable of acquiring subject information for reducing generation of artifacts without increasing the number of wires connected to the outside. Provided is a probe including a plurality of ultrasonic transducers, wherein the ultrasonic transducers are divided into a plurality of groups, two adjoining ultrasonic transducers belong to different groups, and the probe includes a group selection unit configured to switch signals of the ultrasonic transducers to be outputtable for each of the groups.

The present invention relates to a breast cancer diagnosis device. More particularly, the present invention relates to a breast cancer diagnosis device for early detection of the presence or absence of breast cancer lesions inside the breast of a diagnosis subject. The breast cancer diagnosis device includes: an X-ray diagnosis unit generating an X-ray image of a diagnosis subject; an optical diagnosis unit generating an optical transmission image of the diagnosis subject; and a transfer unit which is coupled to the X-ray diagnosis unit and the optical diagnosis unit to transfer all or part of the X-ray diagnosis unit and the optical diagnosis unit, and sequentially transfer all or part of the X-ray diagnosis unit or the optical diagnosis unit toward the diagnosis subject.