TY - GEN
T1 - Cone beam breast CT with a flat panel detector- Simulation, implementation and demonstration
AU - Shaw, Chris C.
AU - Chen, Lingyun
AU - Altunbas, Mastafa C.
AU - Tu, Shuju
AU - Liu, Xinming
AU - Wang, Tian Peng
AU - Lai, Chao Jen
AU - Kappadath, S. Cheenu
AU - Meng, Yang
PY - 2005
Y1 - 2005
N2 - This paper describes our experiences in the simulation, implementation and application of a flat panel detector based cone beam computed tomography (CT) imaging system for dedicated 3-D breast imaging. In our simulation study, the breast was analytically modeled as a cylinder of breast tissue loosely molded into cylindrical shape with embedded soft tissue masses and calcifications. Attenuation coefficients for various types of breast tissue, soft tissue masses and calcifications were estimated for various kVp's to generate simulated image signals. Projection images were computed to incorporate x-ray attenuation, geometric magnification, x-ray detection, detector blurring, image pixelization and digitization. Based on the x-ray kVp/filtration used, transmittance through the phantom, detective quantum efficiency (DQE), exposure level, and imaging geometry, the photon fluence was estimated and used to compute the quantum noise level on a pixel-by-pixel basis for various dose levels at the isocenter. This estimated noise level was then used with a random number generator to generate and add a fluctuation component to the noiseless transmitted image signal. The noise carrying projection images were then convolved with a Gaussian-like kernel, computed from measured 1-D line spread function (LSF) to simulate detector blurring. Additional 2-D Gaussian filtering was applied to the projection images and tested for improving the detection of soft tissue masses and calcifications in the reconstructed images. Reconstruction was performed using the Feldkamp filtered backprojection algorithm. All simulations were performed on a 24 PC (2.4 GHz Dual-Xeon CPU) cluster with MPI parallel programming. With 600 mrads mean glandular dose (MGD) at the phantom center, soft tissue masses as small as 1 mm in diameter could be visualized in a 10 cm diameter 50% glandular 50% adipose or fatter breast tissue, and 2 mm or larger masses were visible in a 100% glandular 0% adipose breast tissue. We have also demonstrated that 0.15 mm or larger calcification could be detected with a 100 μm detector pixel size while 0.2 mm or larger calcifications were visible with a pixel size of 200 μm. Our simulation study has shown that the cone-beam CT breast imaging can provide reasonable good quality and detectability at a dose level similar to that of two views mammography. For imaging experiments, a stationary x-ray source and detector, a stationary gantry, rotating phantom system was constructed to demonstrate cone beambreast CT imaging. Breast specimens from mastectomy were imaged to demonstrate the superior tissue contrast that can be achieved with the cone beam CT technique. Various phantoms were imaged to demonstrate that calcifications as small as 280 μm could be imaged at 80 kVp with a voxel size of 140 μm with an estimated isocenter dose of 1.8 rad.
AB - This paper describes our experiences in the simulation, implementation and application of a flat panel detector based cone beam computed tomography (CT) imaging system for dedicated 3-D breast imaging. In our simulation study, the breast was analytically modeled as a cylinder of breast tissue loosely molded into cylindrical shape with embedded soft tissue masses and calcifications. Attenuation coefficients for various types of breast tissue, soft tissue masses and calcifications were estimated for various kVp's to generate simulated image signals. Projection images were computed to incorporate x-ray attenuation, geometric magnification, x-ray detection, detector blurring, image pixelization and digitization. Based on the x-ray kVp/filtration used, transmittance through the phantom, detective quantum efficiency (DQE), exposure level, and imaging geometry, the photon fluence was estimated and used to compute the quantum noise level on a pixel-by-pixel basis for various dose levels at the isocenter. This estimated noise level was then used with a random number generator to generate and add a fluctuation component to the noiseless transmitted image signal. The noise carrying projection images were then convolved with a Gaussian-like kernel, computed from measured 1-D line spread function (LSF) to simulate detector blurring. Additional 2-D Gaussian filtering was applied to the projection images and tested for improving the detection of soft tissue masses and calcifications in the reconstructed images. Reconstruction was performed using the Feldkamp filtered backprojection algorithm. All simulations were performed on a 24 PC (2.4 GHz Dual-Xeon CPU) cluster with MPI parallel programming. With 600 mrads mean glandular dose (MGD) at the phantom center, soft tissue masses as small as 1 mm in diameter could be visualized in a 10 cm diameter 50% glandular 50% adipose or fatter breast tissue, and 2 mm or larger masses were visible in a 100% glandular 0% adipose breast tissue. We have also demonstrated that 0.15 mm or larger calcification could be detected with a 100 μm detector pixel size while 0.2 mm or larger calcifications were visible with a pixel size of 200 μm. Our simulation study has shown that the cone-beam CT breast imaging can provide reasonable good quality and detectability at a dose level similar to that of two views mammography. For imaging experiments, a stationary x-ray source and detector, a stationary gantry, rotating phantom system was constructed to demonstrate cone beambreast CT imaging. Breast specimens from mastectomy were imaged to demonstrate the superior tissue contrast that can be achieved with the cone beam CT technique. Various phantoms were imaged to demonstrate that calcifications as small as 280 μm could be imaged at 80 kVp with a voxel size of 140 μm with an estimated isocenter dose of 1.8 rad.
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U2 - 10.1109/iembs.2005.1615457
DO - 10.1109/iembs.2005.1615457
M3 - Conference contribution
C2 - 17281227
AN - SCOPUS:33846923145
SN - 0780387406
SN - 9780780387409
T3 - Annual International Conference of the IEEE Engineering in Medicine and Biology - Proceedings
SP - 4461
EP - 4464
BT - Proceedings of the 2005 27th Annual International Conference of the Engineering in Medicine and Biology Society, IEEE-EMBS 2005
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2005 27th Annual International Conference of the Engineering in Medicine and Biology Society, IEEE-EMBS 2005
Y2 - 1 September 2005 through 4 September 2005
ER -