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933.e2  Spinal Malformations, Congenital




            Spinal Malformations, Congenital
  VetBooks.ir


                                                cord. Depending on the degree of compres-
            BASIC INFORMATION
                                                sion,  dogs  show  signs  of  hyperesthesia  or   •  Spinal  dysraphism  is  caused  by  abnormal
                                                                                   closure of the developing neural tube, result-
           Definition                           paresis/plegia.                    ing in a defective neural arch and associated
           A developmental abnormality of the spinal   Abnormalities of spinal cord and meninges:  spinal cord abnormalities.
           cord and/or vertebrae. Malformations of the   •  Spina bifida: failure of closure of the dorsal
           spinal cord are referred to as spinal dysraphism.   aspect of the vertebrae   DIAGNOSIS
           Not all congenital malformations, particularly   ○   Can affect the vertebrae alone; incidental
           vertebral malformations, cause clinical signs. If   radiographic finding  Diagnostic Overview
           signs develop, they are often not detected until   ○   Defect can be associated with protusion of   Slowly progressive neurologic deficits in a young
           early adulthood.                       the meninges (meningocoele) or meninges   animal from an overrepresented breed should
                                                  and  spinal  cord  (meningomyelocele);   raise the suspicion of a congenital vertebral
           Synonyms                               affected animals can exhibit ataxia,   malformation.  Malformations involving the
           Vertebral  malformations,  spinal/vertebral   paraparesis, paraplegia, or incontinence.  spinal cord often present with neurologic
           anomalies, spinal dysraphism       •  Sacrocaudal  dysgenesis:  complex  form  of   deficits at weeks to months of age.
                                                spina bifida with incomplete or absent
           Epidemiology                         formation of the sacral and coccygeal ver-  Differential Diagnosis
           SPECIES, AGE, SEX                    tebrae and associated spinal cord segments.   •  Infectious/inflammatory myelopathies
           Dogs and cats, any sex; age of onset of clinical   Affected animals often have urinary and   •  Congenital spinal cord disorders
           signs is variable, depending on the nature and   fecal incontinence and can have pelvic limbs   •  Traumatic myelopathy
           severity of the anomaly.             deficits.
                                                                                 Initial Database
           GENETICS, BREED PREDISPOSITION     HISTORY, CHIEF COMPLAINT           •  Neurologic examination (p. 1136): findings
           Certain breeds are overrepresented:  •  Most congenital vertebral malformations, if   supporting a myelopathy; neurolocalization
           •  Hemivertebrae:  English  bulldogs,  French   clinically significant, cause a slow, chronic   depends on site of malformation
            bulldogs, pugs, Boston terriers     progression of gait deficits.    •  Spinal  radiographs:  confirm  the  presence
           •  Spina bifida: Manx cats, English bulldogs,   •  Signs  associated  with  spinal  malforma-  of a vertebral malformation. Radiographic
            Rhodesian  ridgebacks  (associated  with   tions are usually present at birth but may   abnormalities can be incidental; further
            dermoid sinus tracts)               not become obvious until the animal   testing is needed in animals with neuro-
           •  Sacrocaudal  dysgenesis:  English  bulldog,   begins to  ambulate  or housebreaking is     logic deficits to investigate whether the
            French bulldog, pug, Manx cat       attempted.                         malformation is the cause of the clinical
           •  Spinal stenosis: basset hounds, Doberman   •  Urinary or fecal incontience can be recog-  signs or another spinal cord disease is
            pinschers, Great Danes              nized at an early age in animals with spinal   present.
                                                abnormalties.
           ASSOCIATED DISORDERS                                                  Advanced or Confirmatory Testing
           Concurrent congenital anomalies of other   PHYSICAL EXAM FINDINGS     •  MRI (p. 1132) can demonstrate any spinal
           regions of the nervous system or other body   •  Various degrees of neurologic abnormality,   cord pathology associated with an anomaly
           systems often occur.                 ranging from none to hyperesthesia to plegia  and helps rule out other structural conditions.
                                              •  Incontinence  is  a  common  finding  with   •  CSF analysis (pp. 1080 and 1323) helps rule
           Clinical Presentation                anomalies affecting the lumbosacral   out inflammatory disease
           DISEASE FORMS/SUBTYPES               intumescence.                    •  CT often is used to aid surgical planning,
           Abnormalities of vertebral and intervertebral   •  Scoliosis  can  be  evident  with  vertebral   if surgery is indicated.
           discs:                               malformations.
           •  Hemivertebrae: failure of formation of one   •  A  fluctuant,  dorsal  midline  mass  can  be    TREATMENT
            sagittal half of the vertebral body. This can   palpable in animals with meningomyelocele.
            lead to vertebral instability and clinical signs   Uncommonly,  a  fistula  connecting  to  the   Treatment Overview
            of myelopathy, which often are not present   skin on the dorsal midline occurs, with   If clinical signs are present and progres-
            until 1 year of age.                continuous  leakage  of  cerebrospinal  fluid   sive, surgery is often indicated for vertebral
           •  Butterfly vertebrae: failure of formation of a   (CSF).            anomalies. Depending on the malformation,
            portion of vertebral body, with a sagittal cleft                     decompressive surgery or stabilizing techniques
            in vertebral body apparent on ventrodorsal   Etiology and Pathophysiology  are used. Alternatively, a conservative approach
            radiographs; can cause kyphosis but no   •  Genetic defects are suspected, but mode of   consisting of 8 weeks of crate rest and admin-
            neurologic deficits                 inheritance or exact genetic mutation has   istration of analgesics in combination with a
           •  Block vertebrae: failure of segmentation of   not been identified.  nonsteroidal antiinflammatory drug (NSAID)
            adjacent vertebrae; usually not clinically   •  Vertebral  anomalies  that  occur  during   or glucocorticoids can be tried. No treatment
            significant                         embryonic development are associated with   is possible for most malformations that involve
           •  Transitional vertebrae: vertebrae at the cer-  defects  in  formation  (butterfly  vertebrae,   the spinal cord.
            vicothoracic, thoracolumbar, or lumbosacral   hemivertebrae); can also see neural tube
            junction that show anatomic characteristics   defects resulting in spinal dysraphism.   Acute General Treatment
            of an adjacent vertebral spinal segment (e.g.,   Vertebral  anomalies  that  occur  during   Pain medication as needed
            lumbar vertebra with a rib). They usually are   fetal development are associated primarily
            not clinically signficant.          with defects in segmentation and, to a   Chronic Treatment
           •  Spinal stenosis: narrowing of the vertebral   lesser  extent,  formation  (block  vertebrae,   General nursing care, as indicated for animal
            canal; can result in compression of the spinal   transitional vertebrae, spinal stenosis).  with spinal cord disease:

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