Case Report
Copyright ©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Jun 14, 2014; 20(22): 7049-7054
Published online Jun 14, 2014. doi: 10.3748/wjg.v20.i22.7049
Figure 1
Figure 1 Abdominal magnetic resonance at diagnosis and after ten months of treatment. A: Multiple hepatic lesions with heterogeneous characteristics: central hypodensity and peripheral hyperdensity (arrows); B: Stable disease, with a greater contrast between central and peripheral parts of the lesion as colliquative necrosis (arrows).
Figure 2
Figure 2 Ultrasound and contrast-enhanced ultrasound of the liver at diagnosis, six months after the beginning of treatment, five months after lenalidomide interruption, and six months after lenalidomide reintroduction. A: Multiple lesions visualized in the arterial phase (arrows); B: Stable disease (arrow); C: Target lesion is increased (32.9 mm now vs 22.8 mm previously) (arrow); D: Target lesion is slightly decreased in size again (28.1 mm) (arrow).
Figure 3
Figure 3 Pathological and immunohistochemical evaluation. A: Hematoxylin-eosin section at 100 microscopic fields; B Hematoxylin-eosin section at 200 microscopic fields; C: Immunohistochemical expression of vascular cell marker CD34 at 200 microscopic fields (APAAP technique; Gill’s hematoxylin nuclear counterstain); D: Neoplastic cells showing a low proliferation index/MIB1 at 200 microscopic fields (APAAP technique; Gill’s hematoxylin nuclear counterstain). APAAP: Alkaline phosphatase monoclonal anti-alkaline phosphatase.