Open Access BASE2011

THE UF FAMILY OF HYBRID PHANTOMS OF THE DEVELOPING HUMAN FETUS FOR COMPUTATIONAL RADIATION DOSIMETRY

Abstract

Historically, the development of computational phantoms for radiation dosimetry have primarily been directed at capturing and representing adult and pediatric anatomy, with less emphasis devoted to models of the human fetus. As concern grows over possible radiation-induced cancers from medical and non-medical exposures of the pregnant female, the need to better quantify fetal radiation doses, particularly at the organ-level, also increases. Studies such as the European Union's SOLO (Epidemiological Studies of Exposed Southern Urals Populations) hope to improve our understanding of cancer risks following chronic in-utero radiation exposure. For projects like SOLO, currently available fetal anatomic models do not provide sufficient anatomical detail for organ-level dose assessment. To address this need, two fetal hybrid computational phantoms were constructed using high-quality magnetic resonance imaging (MRI) and computed tomography (CT) image sets obtained for two well-preserved fetal specimens aged 11.5 and 21 weeks post-conception. Individual soft tissue organs, bone sites, and outer body contours were segmented from these images using 3D-DOCTORTM and then imported to the 3D modeling software package RhinocerosTM for further modeling and conversion of soft tissue organs, certain bone sites, and outer body contours to deformable non-uniform rational B-spline (NURBS) surfaces. The two specimen-specific phantoms, along with a modified version of the 38-week UF hybrid newborn phantom, comprised a set of base phantoms from which a series of hybrid computational phantoms was derived for fetal ages 8, 10, 15, 20, 25, 30, 35 and 38 weeks post-conception. The methodology used to construct the series of phantoms accounted for the following age-dependent parameters: (1) variations in skeletal size and proportion, (2) bone-dependent variations in relative levels of bone growth, (3) variations in individual organ masses and total fetal masses and (4) statistical percentile variations in skeletal size, individual organ ...

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