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3.4




            Neoplasia


















            Extradural neoplasia                                 CT features of primary bone tumors include hetero­
                                                               geneous osteolysis of affected bone with periosteal and
            Juxtavertebral neoplasia                           endosteal reactive bone formation. Amorphous tumor
            Malignant soft‐tissue neoplasms that arise adjacent to   new bone may also be present in osteoblastic tumors
            the vertebral column can invade vertebrae and the verte­  (Figures 3.4.5, 3.4.6, 3.4.7). 2,3
            bral  canal. Such neoplasms are often mesenchymal in   MR features include altered anatomic margins and T1
            origin  and  include  hemangiosarcoma,  fibrosarcoma,   and T2 hypointensity in regions of reactive and tumor
            myxosarcoma, liposarcoma, and synovial tumors      new bone formation. When the tumor mass includes a
            (Figures 3.4.1, 3.4.2, 3.4.3).                     significant vascular soft‐tissue component, that region
                                                               will have variable T1 and T2 intensity and can heteroge­
            Neoplasia arising from bone                        neously contrast enhance (Figure 3.4.7). 4,5
            Benign primary bone tumors
            The clinical significance of benign bone tumors, such as   Plasma cell tumors
            vertebral osteomas and osteochondromas, often depends   Plasma cell neoplasms arise from malignant proliferation
            on whether they encroach on the spinal cord or disrupt   of B‐lymphocytes, and they may occur as solitary plasma­
            the structural integrity of the vertebral column. Benign   cytomas or multiple myeloma. Multiple myeloma typically
            bone tumors are usually highly mineralized, smoothly   affects bone, including vertebrae, ribs, pelvis, skull, and
            margined, and have CT attenuation and MR intensities   proximal or distal aspects of long bones, while plasmacy­
            similar to those of normal dense bone (Figure 3.4.4). 1  tomas may occur in the skin, mucosa, gastrointestinal
                                                               tract, and bone. Plasmacytomas of the vertebral column
            Malignant primary bone tumors                      generally arise from a single vertebra but can involve
            Primary bone tumors arising from the vertebral column     adjacent segments. Multiple myeloma is multifocal and
            include osteosarcoma, chondrosarcoma, and fibrosar­  polyostotic and is usually widely distributed within both
            coma and typically have aggressive imaging features.   axial and appendicular bone.
            Those tumors  with  significant  osteoid  production will   CT and MR are superior to survey radiography for
            appear predominantly osteoproductive or have osteopro­  determining the presence and size of vertebral plasma
            ductive/osteolytic components, while others may have a   cell tumors.  CT features of plasmacytoma include
                                                                         6
            predominantly osteolytic appearance. Tumors arise from     osteolysis, often associated with preservation of at least
            a single vertebra, but reactivity or invasion of adjacent   part of the cortical margin, and pathologic fractures are
            vertebrae may occur. Extension into the vertebral canal   common. Tumor mass can also breach the cortical
            can cause spinal cord compression, and pathologic frac­    margin  and encroach  on the vertebral canal, causing
            ture can occur because of loss of structural integrity of   extradural spinal cord compression. Plasmacytomas are
            the vertebral body.                                soft‐tissue attenuating and mildly to markedly enhance

            Atlas of Small Animal CT and MRI, First Edition. Erik R. Wisner and Allison L. Zwingenberger.
            © 2015 John Wiley & Sons, Inc. Published 2015 by John Wiley & Sons, Inc.
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