Single-photon emission tomographic imaging subdivides into two classes of technique: transverse-section computed tomography and longitudinal-section tomography. Longitudinal tomography can be achieved by combining a gamma camera with a spatially or time coded aperture or with a segmented multiple-pinhole collimator (Budinger, 1980). Longitudinal imaging using the latter type of collimator generates spatially distinct camera images. The reconstruction of longitudinal sections from such non-overlapping images does not necessitate decoding of an aperture function. Instead, reconstruction proceeds by iteration and, in principle, provided criteria for depth resolution are met, complete decoupling of reconstructed planes (blur-free imaging) results. For identifying lesions the absence of blurring artefacts is a great advantage over coded aperture imaging in which it is difficult to completely decouple planes (Webb et al., 1978); additionally, multiple-pinhole tomography can quantitatively map out the uptake of a radionuclide in organs and tumours. To date several workers, notably including Vogel et al. (1978, 1979), have concentrated on the development and application of a seven-pinhole aperture for myocardial imaging. Limited by a very small field of view, the seven-pinhole aperture has not found wider application in nuclear medicine. In this note an imaging technique based on the use of an aperture comprising three pinholes arranged in a triangle is proposed which overcomes this limitation and can lead directly to an extension of quantitative, completely decoupled, longitudinal tomography into other important fields of nuclear medicine.
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