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CHAPTER 65   Disorders of the Spinal Cord  1155


            Syringomyelia/Hydromyelia                                       Ventricular dilation
            Cystic accumulations of fluid within the spinal cord causing                Supraoccipital bone
  VetBooks.ir  compression of adjacent parenchyma are being recognized                         Chiari malformation
            with increasing frequency as advanced diagnostic imaging
            techniques (i.e., CT, MRI) are used for neurologic diagnosis.
            Syringomyelia is development of a CSF-filled cavity (syrinx)
            within the parenchyma of the spinal cord, and hydromyelia                          *
            is accumulation of excessive CSF within a dilated central
            canal. These disorders can develop as a result of altered                Basioccipital bone
            CSF pressures within the spinal canal, a loss of spinal cord
            parenchyma, or secondary to obstructed CSF flow caused   FIG 65.25
            by congenital malformations,  trauma,  or inflammatory  or   Midsagitally T2-weighted magnetic resonance imaging of
            neoplastic disorders. A relatively common cause of syrin-  the brain and upper cervical spinal cord from a 3-year-old
            gomyelia in dogs is a malformation of the skull (Chiari-like   Cavalier King Charles Spaniel with Chiari-like malformation
            malformation [CM]) that reduces the volume of the caudal   and syringomyelia (asterisk). (From Bonagura J, Twedt D:
            fossa and displaces the cerebellum and brainstem into the   Current veterinary therapy XIV, St Louis, Elsevier, 2009, p
                                                                 1102.)
            foramen magnum, obstructing CSF movement. The CSF,
            which normally flows through the foramen magnum during
            systole, becomes turbulent at the craniocervical junction,
            leading to syrinx formation. This disorder is inherited in   CONGENITAL NONPROGRESSIVE
            the Cavalier King Charles Spaniel (CKCS). More than 95%   DISORDERS IN YOUNG ANIMALS
            of CKCS dogs have some degree of CM, 50% of those dogs   Spina Bifida
            have syringomyelia, and 35% of affected CKCS dogs show    Spina bifida results from embryonic failure of fusion of the
            clinical signs.                                      two halves of the dorsal spinous processes of the vertebral
              Onset of clinical signs is usually in puppies and young-  arch. Although spina bifida may occur anywhere along the
            adult CKCS dogs, with most dogs showing signs before 4   spinal canal, the caudal lumbar and lumbosacral region is
            years of age. The most consistent sign is neck pain that can   most often affected. This malformation is most common in
            be constant or intermittent. Some dogs randomly vocal-  English Bulldogs and Manx cats. In the Manx cat, the con-
            ize or resent touching of the ear, limb, face, or neck of   dition is an autosomal recessive trait and may be associated
            the affected side. Others scratch repeatedly at their neck   with caudal agenesis. Clinical signs are nonprogressive and
            or shoulder, often without making skin contact (phantom   present from birth, including rear limb LMN paresis, fecal
            scratching). Muscle atrophy and LMN weakness of the   and  urinary  incontinence,  loss  of  perineal  sensation,  and
            associated thoracic limb, and ataxia and UMN deficits of   decreased tone of the anal sphincter. No therapy is available.
            the rear limbs may also be seen. Scoliosis may develop as
            LMN  damage  within  the  cord  causes  asymmetric  dener-  Caudal Agenesis of Manx Cats
            vation of the paraspinal muscles, resulting in vertebral     Congenital malformations of the sacrococcygeal spinal cord
            deviation.                                           and vertebrae are common in tailless Manx cats. Clinical
              CM and syringomyelia are hereditary conditions in the   signs result from agenesis or dysgenesis of the caudal verte-
            CKCS, suggested to be autosomal recessive with incomplete   brae and sacral spinal cord. Signs are typically present from
            penetrance. Diagnosis is most reliably made with MRI,   birth and include hopping or crouched pelvic limb gait, fecal
            which shows a small caudal fossa secondary to a hypoplastic   and urinary incontinence, and chronic constipation.
            occipital bone, cerebellar crowding, and cerebellar compres-
            sion or herniation through the foramen magnum (Fig.   Spinal Dysraphism
            65.25). Fluid-filled cavities (syrinxes) are sometimes identi-  Spinal dysraphism is an inherited congenital malformation
            fied within the spinal cord parenchyma, particularly in cervi-  of the spinal cord. It results from abnormal development of
            cal regions. Maximum syrinx width is a strong predictor of   the structures of the spinal cord along the central plane. The
            the severity of signs in affected dogs.              malformation includes a dilated or absent central canal, cavi-
              Treatment is aimed at relieving pain and other neurologic   tation in the white matter, and the abnormal presence of
            signs. Analgesics such as NSAIDs, tramadol, gabapentin, or   ventral gray column cells across the median plane between
            pregabalin may be recommended. Drugs to decrease CSF   the central canal and the ventral median fissure. Spinal dys-
            production (omeprazole, acetazolamide, prednisone) may   raphism is recognized most commonly in Weimaraners,
            also result in clinical improvement. If medical treatment   although other breeds are occasionally affected.
            does not alleviate the clinical signs, decompression of the   Clinical signs are present at birth. Affected dogs have a
            caudal fossa with an occipital craniectomy to reestablish   symmetric bunny-hopping pelvic limb gait, a wide-based
            normal CSF flow can be effective, but recurrence is common   stance, and depressed proprioception. The patellar reflex is
            in the long term and neuropathic pain may persist, requiring   normal. The pelvic limb flexor reflex stimulated in one limb
            continued medical treatment.                         usually elicits simultaneous flexion of both pelvic limbs.
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