Method and device to generate spatially resolved quasi-T2-weighted magnetic resonance signals

1. A method to generate spatially resolved, quasi-T2-weighted magnetic resonance signals from an examination region of a subject, comprising:

operating a magnetic resonance data acquisition unit with a first gradient-balanced SSFP sequence in which an initial magnetization in the subject is flipped in a first direction;

operating said magnetic resonance data acquisition unit to detect spatially coded first magnetic resonance signals from the first gradient-balanced SSFP sequence during a transient portion of said first gradient-balanced SSFP sequence;

operating said magnetic resonance data acquisition unit with a second gradient-balanced SSFP sequence with which said initial magnetization is flipped in a direction opposite said first direction, said second gradient-balanced SSFP sequence being of a same sequence type as said first gradient-balanced SSFP sequence;

operating said magnetic resonance data acquisition unit to detect spatially coded second magnetic resonance signals from said gradient-balanced SSFP sequence during a transient portion of said second gradient-balanced SSFP sequence;

in a computerized processor, constructively superimposing said first and second magnetic resonance signals to form overlay signals; and

in said processor, processing said overlay signals into image data with a predominant T2 weighting or for spatially resolved estimation of a T2 relaxation time constant, and making said image data or said estimation of said T2 relaxation time constant available at an output of said processor.

2. A method as claimed in claim 1 comprising constructively superimposing said first and second magnetic resonance signals by adding said first and second magnetic resonance signals, if said first and second magnetic resonance signals initially have an identical phase position.

3. A method as claimed in claim 1 comprising constructively superimposing said first and second magnetic resonance signals by forming a difference between said first and second magnetic resonance signals, if said first and second magnetic resonance signals initially have an opposite phase position.

4. A method as claimed in claim 1 comprising producing said first direction of said initial magnetization by a first preparation pulse in said first gradient-balanced SSFP sequence, and producing said second direction of said initial magnetization with a second preparation pulse in said second gradient-balanced SSFP sequence, with each of said first and second preparation pulses being followed in the respective first and second gradient-balanced SSFP sequences by identical excitation pulses.

5. A method as claimed in claim 4 wherein said preparation pulse in said second gradient-balanced SSFP sequence comprises a 180° inversion pulse with a subsequent spoiler pulse.

6. A method as claimed in claim 1 wherein said first and second gradient-balanced SSFP sequences are of the CARR-Purcell-Meiboom-Gill sequence type.

7. A method as claimed in claim 1 wherein said first and second gradient-balanced SSFP sequences are of the CARR-Purcell-Freeman-Hill sequence type.

8. A method as claimed in claim 1 comprising producing a flip angle of said magnetization in said first gradient-balanced SSFP sequence that is half of a subsequent refocusing flip angle and wherein a value of said first flip angle in said second gradient-balanced SSFP sequence is equal to 180° minus half of said subsequent refocusing flip angle.

9. A method as claimed in claim 1 comprising processing said first and second magnetic resonance signals using a partial Fourier technique.

10. A method as claimed in claim 1 comprising generating and processing said first and second magnetic resonance signals using a partially parallel acquisition technique.

11. A method as claimed in claim 1 wherein said examination area exhibits a periodic movement, and comprising triggering acquisition of said first and second magnetic resonance signals dependent on said movement.

12. A method as claimed in claim 11 comprising starting signal acquisition with each of said first and second gradient-balanced SSFP sequences in a movement phase and acquiring said first and second magnetic resonance signals in a phase of relative rest of said movement.

13. A method as claimed in claim 12 comprising acquiring said first and second magnetic resonance signals over a plurality of cycles of said movement in segmented k-space according to the pairing principle.

14. A device to generate spatially resolved, quasi-T2-weighted magnetic resonance signals from an examination region of a subject, comprising:

a magnetic resonance data acquisition unit operated by a control unit;

said control unit being configured to operate a magnetic resonance data acquisition unit with a first gradient-balanced SSFP sequence in which an initial magnetization in the subject is flipped in a first direction;

said control unit being configured to operate said magnetic resonance data acquisition unit to detect spatially coded first magnetic resonance signals from the first gradient-balanced SSFP sequence during a transient portion of said first gradient-balanced SSFP sequence;

said control unit being configured to operate said magnetic resonance data acquisition unit with a second gradient-balanced SSFP sequence with which said initial magnetization is flipped in a direction opposite said first direction, said second gradient-balanced SSFP sequence being of a same sequence type as said first gradient-balanced SSFP sequence;

said control unit being configured to operate said magnetic resonance data acquisition unit to detect spatially coded second magnetic resonance signals from said gradient-balanced SSFP sequence during a transient portion of said second gradient-balanced SSFP sequence;

a computerized processor configured to constructively superimpose said first and second magnetic resonance signals to form overlay signals; and

said processor being configured to process said overlay signals into image data with a predominant T2 weighting or for spatially resolved estimation of a T2 relaxation time constant, and making said image data or said estimation of said T2 relaxation time constant available at an output of said processor.