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 "excerpt": "Tomosynthesis is an X-ray technique that reconstructs cross-sectional slices from a limited-angle tube sweep, used mainly as digital breast tomosynthesis for screening and chest tomosynthesis for lung nodules.",
 "snippet": "Tomosynthesis is an X-ray technique that reconstructs cross-sectional slices from a limited-angle tube sweep, used mainly as digital breast tomosynthesis for screening and chest tomosynthesis for lung nodules.",
 "node": "life.health.clinical.clinical-imaging.radiography-and-projection-imaging",
 "markdown": "# Tomosynthesis\n\nTomosynthesis is an X-ray imaging technique that reconstructs a stack of cross-sectional slices from a series of projection radiographs acquired during a single, limited-angle sweep of the x-ray tube. It is best known as digital breast tomosynthesis (DBT) for breast cancer screening and as chest tomosynthesis for lung nodule detection, and it sits between a plain radiograph, which superimposes all tissue in one image, and computed tomography (CT), which reconstructs a true three-dimensional volume from a full rotation.<sup>[1](https://doi.org/10.1088/0031-9155/48/19/r01)</sup> The reconstructed stack is a set of roughly 1-mm-thick slices in which tissue in the plane is sharp and detail above and below is blurred.<sup>[2](https://www.journalslibrary.nihr.ac.uk/hta/HTA19040)</sup>\n\n| Key fact | Detail |\n|---|---|\n| Output | A reconstructed 3D volume of ~1-mm sections whose depth resolution is limited by the limited-angle acquisition<sup>[2](https://www.journalslibrary.nihr.ac.uk/hta/HTA19040)</sup><sup> • </sup><sup>[3](https://pmc.ncbi.nlm.nih.gov/articles/PMC8170874/)</sup> |\n| Acquisition | X-ray tube sweeps a 15°–60° arc (vendor-dependent), acquiring multiple low-dose projections<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> |\n| Reconstruction | Filtered backprojection or iterative algorithms; 1-mm sections<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> |\n| Screening yield | Cancer detection 6.36–7.40 per 1000 with DBT combinations vs 4.68 for digital mammography alone<sup>[5](https://pmc.ncbi.nlm.nih.gov/articles/PMC8168096/)</sup> |\n| Chest dose | About 0.12 mSv, roughly three times a chest radiograph and far below CT's 4–8 mSv<sup>[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC3693857/)</sup><sup> • </sup><sup>[7](https://atm.amegroups.org/article/view/16290/html)</sup> |\n| Reading cost | Interpretation time nearly doubles (91 s for 2D+DBT vs 45 s for 2D); files 200–450 MB vs 8–24 MB<sup>[2](https://www.journalslibrary.nihr.ac.uk/hta/HTA19040)</sup><sup> • </sup><sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> |\n\n## How it works\n\nThe geometric idea is in-plane focus with out-of-plane blur. Projections taken at different tube angles are shifted by amounts that depend on the height of the plane being reconstructed and then added: structures lying in that plane align across projections and reinforce, while structures at other heights are displaced between projections and smear. The magnitude of the shift applied at plane height H depends on the source-to-image distance, the projection angle, and the separation between H and the center of the reconstruction plane.<sup>[8](https://www.mdpi.com/1999-4893/17/2/71)</sup> Because an arbitrary number of in-focus planes can be generated retrospectively from one tube motion, tomosynthesis improves on conventional geometric tomography.<sup>[1](https://doi.org/10.1088/0031-9155/48/19/r01)</sup>\n\nBeyond this shift-and-add backprojection, the main deblurring algorithms are matrix inversion tomosynthesis (MITS), which solves for out-of-plane blur using matrix algebra in frequency space, and filtered backprojection (FBP), which multiplies the [Fourier transform](https://www.edgepedia.org/fourier-transform) of the projections by a ramp function with a roll-off filter to suppress noise amplification.<sup>[9](https://pmc.ncbi.nlm.nih.gov/articles/PMC2832060/)</sup> In a comparison on a breast prototype, Wu and colleagues<sup>[10](https://doi.org/10.1118/1.1786692)</sup> found that backprojection gives higher signal difference-to-noise ratio for masses but substantial out-of-plane artifacts, FBP improves microcalcification visualization, and maximum-likelihood reconstruction gives the best balance.<sup>[11](https://pubs.rsna.org/doi/10.1148/radiol.2015141303)</sup>\n\n## How it is done\n\nA DBT exam follows the mammography routine up to acquisition. The breast is compressed, and the x-ray tube rotates in an arc of 15 to 60 degrees, the sweep angle depending on the vendor, acquiring multiple low-dose projections aligned to the chest wall with either continuous or step-and-shoot motion.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> In the standard combined protocol, a full-field digital mammography (FFDM) image is acquired first, then the anti-scatter grid is retracted for the tomosynthesis scan.<sup>[12](http://mpijournal.org/pdf/2014-01/MPI-2014-01-p057.pdf)</sup> [Reconstruction](https://www.edgepedia.org/reconstruction) then produces 1-mm sections, which the reader scrolls through; a synthetic 2D mammogram can be generated from the same projections instead of a separate FFDM exposure.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup><sup> • </sup><sup>[12](http://mpijournal.org/pdf/2014-01/MPI-2014-01-p057.pdf)</sup>\n\n## Origin\n\nReconstructing longitudinal planes from a set of projection images goes back many decades, and tomosynthesis is a refinement of conventional geometric tomography, which has been known since the 1930s.<sup>[1](https://doi.org/10.1088/0031-9155/48/19/r01)</sup><sup> • </sup><sup>[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC3693857/)</sup> The term and simple tomosynthesis reconstruction were introduced by David G. Grant in 1972 in IEEE Transactions on Biomedical Engineering; the name combines the Greek \"tomos\" (a section, a slice, cutting) and \"synthesis\" (a process).<sup>[13](https://doi.org/10.1109/tbme.1972.324154)</sup><sup> • </sup><sup>[7](https://atm.amegroups.org/article/view/16290/html)</sup> Film-based clinical prototypes were built in the 1970s and 1980s.<sup>[12](http://mpijournal.org/pdf/2014-01/MPI-2014-01-p057.pdf)</sup> James T. Dobbins and Devon J. Godfrey published the field's comprehensive review, \"Digital x-ray tomosynthesis: current state of the art and clinical potential,\" in Physics in Medicine and Biology in 2003.<sup>[1](https://doi.org/10.1088/0031-9155/48/19/r01)</sup> Niklason and colleagues published \"Digital tomosynthesis in breast imaging\" in [Radiology](https://www.edgepedia.org/radiology) in 1997, the feasibility study that launched DBT, acquiring low-dose images in a step-and-expose arc above the stationary breast and detector.<sup>[14](https://doi.org/10.1148/radiology.205.2.9356620)</sup> The enabling hardware was the flat-panel detector; spiral CT's rise in the late 1980s had halted tomosynthesis research for about a decade until flat-panel detectors arrived in the late 1990s.<sup>[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC3693857/)</sup><sup> • </sup><sup>[9](https://pmc.ncbi.nlm.nih.gov/articles/PMC2832060/)</sup> The first US DBT system, the Hologic Selenia Dimensions, was FDA-approved for screening in February 2011.<sup>[15](https://academic.oup.com/bjr/article/98/1175/1963/8229565)</sup> A 2025 historical review of the evolution of tomosynthesis was published by Mitchell M. Goodsitt and Andrew D. A. Maidment in the Journal of Medical Imaging.<sup>[16](https://doi.org/10.1117/1.jmi.12.s1.s13012)</sup>\n\n## Variants\n\nSynthetic mammography (SM) renders the tomosynthesis source projections into a maximum-intensity-projection-like image that simulates a 2D mammogram, cutting overall dose by roughly one half; C-View software was FDA-approved to replace the FFDM image of the combined FFDM-tomosynthesis exam with a synthetic 2D.<sup>[3](https://pmc.ncbi.nlm.nih.gov/articles/PMC8170874/)</sup><sup> • </sup><sup>[12](http://mpijournal.org/pdf/2014-01/MPI-2014-01-p057.pdf)</sup><sup> • </sup><sup>[15](https://academic.oup.com/bjr/article/98/1175/1963/8229565)</sup> As of 2020, four FDA-approved DBT systems were available in the United States, differing in tube motion, filter and detector material, pixel size and binning, and reconstruction.<sup>[3](https://pmc.ncbi.nlm.nih.gov/articles/PMC8170874/)</sup>\n\nContrast-enhanced DBT (CE-DBT) adds iodinated contrast; a pilot in 13 patients with BI-RADS 4 or 5 lesions acquired 9 images over a 50° arc per data set at a dose comparable to two mammographic views.<sup>[17](https://pmc.ncbi.nlm.nih.gov/articles/PMC1850283/)</sup> Dual-energy CE-DBT acquires seven images in 6.7° increments over a 40° arc and is less susceptible to motion artifacts than temporal subtraction because both energy images are acquired after injection.<sup>[18](https://pmc.ncbi.nlm.nih.gov/articles/PMC3473453/)</sup> Photon-counting DBT acquires low- and high-energy projections simultaneously in one scan by covering alternate slits of a 48-slit collimator with tin and copper filters.<sup>[19](https://pubmed.ncbi.nlm.nih.gov/21158302/)</sup> Stationary DBT replaces tube motion with multiple sources; a second-generation system with faster scan time and wider angular span was reported by Calliste and colleagues in 2017 in Medical Physics.<sup>[20](https://doi.org/10.1002/mp.12393)</sup> In chest imaging, a multi-source prototype uses 5 independently moving x-ray sources over a 60° span, scanning in 2–6 s where commercial single-source systems need at least 10 s and at most 40°.<sup>[21](https://pmc.ncbi.nlm.nih.gov/articles/PMC11225395/)</sup>\n\n## Applications\n\nA meta-analysis of 42 studies covering 2,606,296 screened patients with 13,003 cancers found a cancer detection rate of 6.36 per 1000 for DBT plus digital mammography and 7.40 per 1000 for DBT plus synthetic 2D, versus 4.68 per 1000 for digital mammography alone; recall was lowest for DBT+S2D at 42.3 per 1000 versus 78.8 for mammography alone.<sup>[5](https://pmc.ncbi.nlm.nih.gov/articles/PMC8168096/)</sup> DBT alone showed no statistically significant benefit over mammography alone for detection rate, recall, or positive predictive value.<sup>[5](https://pmc.ncbi.nlm.nih.gov/articles/PMC8168096/)</sup> Ciatto and colleagues reported the STORM prospective comparison study in The Lancet Oncology in 2013, integrating 3D mammography with tomosynthesis for population screening.<sup>[22](https://doi.org/10.1016/s1470-2045%2813%2970134-7)</sup> Trial results agree in direction: in the RETomo randomized trial, detection was 8.6 vs 4.5 per 1000 with recall equal at 3.5% in both arms;<sup>[23](https://pubs.rsna.org/doi/10.1148/radiol.2018172119)</sup> in the German TOSYMA trial of 99,689 women, invasive cancer detection was 7.1 vs 4.8 per 1000 with DBT plus synthesized 2D.<sup>[24](https://pubmed.ncbi.nlm.nih.gov/35427470/)</sup>\n\nIn the chest, a [Gothenburg](https://www.edgepedia.org/gothenburg) observer study of 89 subjects found three times as many lung nodules detected by tomosynthesis as by chest radiography at an average effective dose of 0.12 mSv.<sup>[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC3693857/)</sup> DBT is also used for tomosynthesis-guided core biopsy, which yields near 100% and takes less than half the time of stereotactic biopsy.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> Despite these results, DBT is not yet implemented in most state or national breast screening programs.<sup>[25](https://iopscience.iop.org/article/10.1088/1361-6560/ac9a35)</sup>\n\n## Limitations and alternatives\n\nLimited-angle acquisition is the root constraint: depth resolution is inferior to CT, so objects can appear in more than one section, pleural versus subpleural nodule location is hard to distinguish, and motion artifacts are relatively common.<sup>[7](https://atm.amegroups.org/article/view/16290/html)</sup> Geometry trades off resolution: a wider sweep angle improves tomographic separation and z-axis resolution but reduces in-plane resolution for microcalcifications, while more projections raise in-plane resolution and dose.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup> DBT alone is not reliable for detecting or characterizing microcalcifications, for which FFDM with spot magnification views remains the standard; the minimum detectable calcification diameter is 164 ± 5 µm for digital mammography versus 210 ± 5 µm for DBT at standard dose.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup><sup> • </sup><sup>[26](https://www.dovepress.com/the-role-of-digital-breast-tomosynthesis-in-breast-cancer-screening-a--peer-reviewed-fulltext-article-CMAR)</sup>\n\nAdding two tomosynthesis views to 2D mammography roughly doubles dose while staying below the FDA's 3 mGy/view limit; in an intraindividual comparison in 389 women, median mean glandular dose per breast was 4.07 mGy for FFDM, 4.97 mGy for DBT alone, and 9.38 mGy for combined FFDM-DBT.<sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup><sup> • </sup><sup>[27](https://ajronline.org/doi/10.2214/AJR.24.32150)</sup> Reading time nearly doubles (91 vs 45 seconds in TOMMY), and DBT files of 200–450 MB versus 8–24 MB for FFDM strain storage and workstations.<sup>[2](https://www.journalslibrary.nihr.ac.uk/hta/HTA19040)</sup><sup> • </sup><sup>[4](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)</sup>\n\nAgainst alternatives: DBT's incremental cancer yield over mammography is lower than that of ultrasound and MRI, and whether DBT improves breast cancer–specific mortality remains unresolved.<sup>[3](https://pmc.ncbi.nlm.nih.gov/articles/PMC8170874/)</sup> In a histopathology-correlated study, DBT and DBT+ultrasound each identified 88.89% of malignant lesions versus 100% for MRI, though DBT takes about 16 seconds for both views versus at least 30 minutes for MRI.<sup>[28](https://pmc.ncbi.nlm.nih.gov/articles/PMC8775881/)</sup>\n\n## References\n\n1. [James T Dobbins, Devon J Godfrey (2003). Digital x-ray tomosynthesis: current state of the art and clinical potential. Physics in Medicine and Biology.](https://doi.org/10.1088/0031-9155/48/19/r01)\n2. [TOMMY trial: A comparison of TOMosynthesis with digital MammographY in the UK NHS Breast Screening Programme (NIHR HTA)](https://www.journalslibrary.nihr.ac.uk/hta/HTA19040)\n3. [Digital Breast Tomosynthesis: Update on Technology, Evidence, and Clinical Practice (Radiology/RadioGraphics 2021)](https://pmc.ncbi.nlm.nih.gov/articles/PMC8170874/)\n4. [Digital Breast Tomosynthesis: an Overview](https://pmc.ncbi.nlm.nih.gov/articles/PMC8272763/)\n5. [Performance of DBT, Synthetic Mammography, and Digital Mammography in Breast Cancer Screening: A Systematic Review and Meta-Analysis](https://pmc.ncbi.nlm.nih.gov/articles/PMC8168096/)\n6. [Chest Tomosynthesis: Technical Principles and Clinical Update](https://pmc.ncbi.nlm.nih.gov/articles/PMC3693857/)\n7. [Digital chest tomosynthesis: the 2017 updated review of an emerging application (Ferrari et al., Ann Transl Med)](https://atm.amegroups.org/article/view/16290/html)\n8. [Algorithms in Tomography and Related Inverse Problems, A Review (Algorithms 2024)](https://www.mdpi.com/1999-4893/17/2/71)\n9. [Tomosynthesis imaging: At a translational crossroads](https://pmc.ncbi.nlm.nih.gov/articles/PMC2832060/)\n10. [Tao Wu and colleagues (2004). A comparison of reconstruction algorithms for breast tomosynthesis. Medical Physics.](https://doi.org/10.1118/1.1786692)\n11. [Digital Breast Tomosynthesis: State of the Art (Vedantham, Karellas, Vijayaraghavan, Kopans; Radiology 2015)](https://pubs.rsna.org/doi/10.1148/radiol.2015141303)\n12. [Digital breast tomosynthesis: TUTORIALS (Medical Physics International)](http://mpijournal.org/pdf/2014-01/MPI-2014-01-p057.pdf)\n13. [David G. Grant (1972). TOMOSYNTHESIS: A Three-Dimensional Radiographic Imaging Technique. IEEE Transactions on Biomedical Engineering.](https://doi.org/10.1109/tbme.1972.324154)\n14. [L T Niklason and colleagues (1997). Digital tomosynthesis in breast imaging.. Radiology.](https://doi.org/10.1148/radiology.205.2.9356620)\n15. [Screening mammography a decade post-tomosynthesis: varied utilization of synthetic mammography across a large health system (British Journal of Radiology 2025)](https://academic.oup.com/bjr/article/98/1175/1963/8229565)\n16. [Mitchell M. Goodsitt, Andrew D. A. Maidment (2025). Evolution of tomosynthesis. Journal of medical imaging.](https://doi.org/10.1117/1.jmi.12.s1.s13012)\n17. [Initial Clinical Experience with Contrast-Enhanced Digital Breast Tomosynthesis](https://pmc.ncbi.nlm.nih.gov/articles/PMC1850283/)\n18. [Dual-energy contrast-enhanced digital breast tomosynthesis – a feasibility study](https://pmc.ncbi.nlm.nih.gov/articles/PMC3473453/)\n19. [Optimization of a dual-energy contrast-enhanced technique for a photon-counting digital breast tomosynthesis system: I. A theoretical model (Carton et al., Med Phys 2010)](https://pubmed.ncbi.nlm.nih.gov/21158302/)\n20. [Jabari Calliste and colleagues (2017). Second generation stationary digital breast tomosynthesis system with faster scan time and wider angular span. Medical Physics.](https://doi.org/10.1002/mp.12393)\n21. [Next-generation digital chest tomosynthesis (multi-source prototype)](https://pmc.ncbi.nlm.nih.gov/articles/PMC11225395/)\n22. [Integration of 3D digital mammography with tomosynthesis for population breast-cancer screening (STORM): a prospective comparison study (The Lancet Oncology, 2013)](https://doi.org/10.1016/s1470-2045%2813%2970134-7)\n23. [Digital Mammography versus Digital Mammography Plus Tomosynthesis for Breast Cancer Screening: The Reggio Emilia Tomosynthesis Randomized Trial (Radiology)](https://pubs.rsna.org/doi/10.1148/radiol.2018172119)\n24. [TOSYMA: DBT plus synthesised mammography versus digital screening mammography for the detection of invasive breast cancer (Lancet Oncology)](https://pubmed.ncbi.nlm.nih.gov/35427470/)\n25. [Performance evaluation of digital breast tomosynthesis systems: physical methods and experimental data (Phys Med Biol 2022)](https://iopscience.iop.org/article/10.1088/1361-6560/ac9a35)\n26. [The role of digital breast tomosynthesis in breast cancer screening: a review (Clinical Medicine Insights: Radiology)](https://www.dovepress.com/the-role-of-digital-breast-tomosynthesis-in-breast-cancer-screening-a--peer-reviewed-fulltext-article-CMAR)\n27. [Digital Mammography, Tomosynthesis, and Contrast-Enhanced Mammography: Intraindividual Comparison of Mean Glandular Dose for Screening Examinations (AJR 2024)](https://ajronline.org/doi/10.2214/AJR.24.32150)\n28. [Comparative Study of Digital Breast Tomosynthesis (DBT) with and without Ultrasound versus Breast MRI in Detecting Breast Lesion](https://pmc.ncbi.nlm.nih.gov/articles/PMC8775881/)\n\n---\n*Topic: Encyclopedia › Life and health › Human health and medicine › Clinical assessment and procedures › Medical imaging and radiography › Radiography and projection imaging*\n\n*Initially written Sep 29, 2026 · Edited: Oct 15, 2026*\n\n*Copyright 2026 EdgeChat AI, a subsidiary of Biostate AI.*\n\nLicense: Edgepedia Community License 1.0, https://www.edgepedia.org/edgepedia/license\n",
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