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Fig. 1 | Surgical Case Reports

Fig. 1

From: A giant pelvic solitary fibrous tumor with Doege–Potter syndrome successfully treated with transcatheter arterial embolization followed by surgical resection: a case report

Fig. 1

Computed tomography (CT) and magnetic resonance imaging (MRI). a Contrast-enhanced CT image showed a hypervascular mass occupying the pelvic cavity, displacing and compressing the rectum (yellow arrows). The tumor showed marked enhancement in a heterogeneous pattern. b T2-weighted pelvic MRI image showed a high-signal-intensity tumor in the pelvis. c 3D-CT image reconstruction showed the tumor occupying the pelvis (green), the tumor-feeding artery (the inferior mesenteric artery colored in red), and the tumor draining vein (the inferior mesenteric vein colored in blue)

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