Page 382 - Atlas of Small Animal CT and MRI
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372  Atlas of Small Animal CT and MRI


              Figure 3.5.15  Disseminated Idiopathic Skeletal Hyperostosis (Canine)                       MR
                                                                              7y M Catahoula Leopard Dog with lumbosa­
                                                                              cral pain. Spinal radiographs reveal dense
                                                                              flowing new bone formation involving the
                                                                              ventral and lateral surfaces of the lumbar ver­
                                                                              tebral bodies (a). The L5–6 intervertebral space
                                                                              is slightly narrow, but there are no other signs
                                                                              indicative of degenerative disease. New bone
                                                                              is hyperintense on the T2 MR image (b). There
                                                                              is heterogeneity to nucleus pulposus intensity
                                                                              in the lumbar spine, but disk architecture
                                                                              appears to be preserved, and the dorsal part of
                                                                              the annulus fibrosis appears normal at each
                                                                              lumbar disk space. There are radiographic and
                                                                              MR imaging features consistent with lumbosa­
             (a) DX, LAT                                                      cral degenerative disease, which was the likely
                                                                              source of clinical signs.



















             (b) T2, SP




































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