AJR:192, May 2009 known, and a strong correlation with another disease process has not been found [3, 4]. SANT has a distinctive gross appearance. It is a well-circumscribed mass composed of numerous nodules derived from red pulp alternating with bands of dense fibrous tissue that coalesce to form a central, stellate fibrous scar [3]. Microscopically, SANT is characterized by multiple nodular aggregates of plump endothelial cells and pericytes lining prominent slitlike vascular spaces [2–5]. The nodules are associated with extravasated erythrocytes, and the intervening collagenous stroma contains variable numbers of reactive myofibroblasts, hemosiderin-laden macrophages, lymphocytes, and plasma cells. The endothelial cells exhibit minimal cytologic atypia, with rare mitotic activity [2–5]. Limited imaging information is conveyed by the pathology literature. Two articles provide correlative enhanced CT images [4, 5]. Both have images or descriptions depicting a hypodense mass in the early portal venous phase, with areas of peripheral enhancement that become homogeneous on more delayed imaging. Description of MR findings in one case indicates that the mass showed low signal on T1 and T2 sequences [4]. A recent report, however, describes a single case showing early peripheral enhancement progressing centripetally in a radial pattern [6]. Although the small number of cases with radiologic description precludes definitive assessment, suggestive characteristics of SANT include a well-circumscribed solitary mass of the spleen that initially shows low attenuation with areas of peripheral enhancement after the administration of contrast material. This may reflect the gross pathologic appearance of central fibrous stroma and more peripheral coalescent nodules of angiomatoid Sclerosing Angiomatoid Nodular Transformation