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816  Section 8  Neurologic Disease

            Table 76.1  Differential diagnosis for acute‐onset myelopathy
  VetBooks.ir  Differential category  Differentials                                      Comments



             Degenerative            Hansen type I intervertebral disc herniation        Asymmetric or symmetric
             Anomalous               Atlantoaxial instability                            Usually symmetric
             Neoplastic              Metastatic, vertebral body tumors, pathologic fracture,   Often asymmetric
                                     histiocytosis, lymphoma, other hematopoietic neoplasia
             Inflammatory            Bacterial, protozoal, and fungal meningomyelitis, canine   Asymmetric or symmetric
             (infectious)            distemper virus, feline infectious peritonitis, discospondylitis,
                                     spinal cord epidural empyema
             Inflammatory            Steroid‐responsive meningitis‐arteritis, granulomatous   Usually symmetric
             (noninfectious)         meningoencephalomyelitis
             Trauma                  Fracture/subluxation, acute noncompressive intervertebral   Asymmetric or symmetric;
                                     disc herniation                                     nonprogressive
             Vascular                Fibrocartilaginous embolism, aortic thromboembolism  Usually asymmetric;
                                                                                         nonprogressive
            Italicized differentials indicate diseases associated with hyperesthesia on spinal palpation.



            Table 76.2  Differential diagnosis for chronic myelopathy

             Differential category  Differentials                                              Comments
             Degenerative (spinal   Degenerative myelopathy, myelinopathy, neuronopathy, axonopathy,   Symmetric
             cord)                subarachnoid diverticulum, storage disorders
             Degenerative         Hansen type II intervertebral disc herniation, cervical spondylomyelopathy   Symmetric or
             (vertebral column)   (wobbler syndrome), degenerative lumbosacral syndrome, spinal synovial cyst,   asymmetric
                                  diffuse idiopathic skeletal hyperostosis, spondylosis deformans,
                                  mucopolysaccharidosis, osteochondromatosis
             Anomalous            Chiari‐like malformation (syringohydromyelia), atlantoaxial instability,   Usually symmetric
                                  vertebral malformation, myelodysplasia, spinal stenosis, dermoid sinus
             Neoplastic           Meningioma, primary spinal cord (oligodendroglioma, astrocytoma,   Often asymmetric
                                  ependymoma), nephroblastoma
             Inflammatory         Bacterial meningomyelitis, canine distemper virus, feline infectious   Asymmetric or
             (infectious)         peritonitis, protozoal, fungal                               symmetric
            Italicized differentials indicate diseases associated with hyperesthesia on spinal palpation.



            General Proprioceptive Ataxia                     Paresis/Plegia
            General proprioceptive (GP) ataxia reflects the lack of   Paresis/plegia is a deficit/loss of ability to carry out vol-
            information reaching the central nervous system   untary motor function. The terms lower motor neuron
            (CNS) responsible for the awareness of movement and   (LMN) and UMN are applied to differentiate two basic
            position of neck, trunk, and  limbs in space. Due to   types  of  neurologic  weakness.  Clinical  signs  of  UMN
            anatomic proximity within the spinal cord of the pro-  weakness are characterized by spasticity with normal to
            prioceptive pathways and motor tracts, propriocep-  increased spinal reflexes and muscular hypertonia. LMN
            tive abnormalities often overlap with those caused by   weakness manifests as flaccidity, hyporeflexia to are-
            upper motor neuron (UMN) weakness. A deficit of GP   flexia  and  muscle  atrophy  that  is  severe  and  rapid  in
            appears  as  misplacement  or  knuckling  of  the  foot,   onset. Neuroanatomic  localization to  a specific spinal
            which may not occur with every step, and poorly con-  cord region is upon UMN or LMN signs (see Table 76.3).
            trolled swaying of the body. The feet may be crossed   In addition, the affected limbs have inadequate or absent
            or placed too far apart. Overall movement of the limbs   voluntary motion, which may be described as monopa-
            lacks coordination.                               resis/plegia (involvement of one limb), paraparesis/
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