Page 411 - Canine Lameness
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21.3  ­Neurorogico  giNciNi  AANicgio ctNe Nolgi  gim  383

             region will produce a bilateral upper motor neuron (UMN)‐paresis (i.e. paraparesis) with general
             proprioceptive (GP) ataxia (Chapter 4). Sensory deficits usually accompany motor deficits. If the
             injury is at the level of the intumescence, multiple spinal cord segments are typically involved in
             most cases, causing a polyneuropathy.
             21.3.1.1  Neoplasia
             Tumors affecting the nervous system of the pelvic limb, either at the intumescence or the nerves,
             commonly cause pelvic limb monoparesis. For any lameness that does not quickly respond to
             empirical therapy, such as anti‐inflammatory medications, neurologic conditions should be con-
             sidered. Particularly in older animals, neoplasia is a common differential diagnosis (Chapter 11).

             21.3.1.2  Spinal Cord Injury
             Hansen Types I and II intervertebral disc herniation (IVDH), acute non‐compressive nucleus pul-
             posus  extrusion  (ANNPE),  and  fibrocartilaginous  embolism  (FCE)  are  also  frequent  causes  of
             myelopathies and radiculopathies affecting the pelvic limbs. The clinical features of these diseases
             are discussed in Chapter 16. Vertebral fracture and luxation (VFL) in the lumbar spine constitute
             almost one‐third of all VFL (Jeffery 2010). Multisite VFL also occurs with some frequency. In con-
             trast to thoracolumbar IVDH, prognosis is grave if nociception is absent secondary to VFL.
               Degenerative myelopathy (DM) can result in LMN paralysis but only with longer disease dura-
             tion (Coates and Wininger 2010). The classic presentation of DM is a slow and progressive clinical
             course with asymmetric signs localizing to the T3–L3 spinal cord segments. Thus, it would not be
             a differential for monoparesis or lameness.

             21.3.1.3  Degenerative Lumbosacral Stenosis and Foraminal Stenosis
             In degenerative lumbosacral stenosis (DLSS; also called lumbosacral disease, lumbosacral instability,
             and cauda equina syndrome), stenosis results from chronic bony and/or soft tissue proliferation,
             especially Type II IVD protrusion, reducing the size of the spinal canal and/or intervertebral fora-
             men, with resulting compression, inflammation, or entrapment of the cauda equina and/or seventh
             lumbar nerve as it exits, respectively (De Risio et al. 2000). This is a disease of older, large‐breed,
             working  dogs,  especially  the  German  Shepherd  Dog,  with  a  predilection  for  males.  The  L7–S1
             intervertebral  disc  (IVD)  is  the  most  commonly  affected  site,  but  any  site  from  L5  to  S3  can  be
             affected. Stenosis of the intervertebral foramen, called foraminal stenosis, can also occur anywhere
             in the lumbar spine but is most prevalent at the L7–S1 and is frequently a component of DLSS. The
             resulting nerve entrapment is a common cause of pelvic limb lameness or monoparesis. Clinical
             signs will be dependent on the specific nerves roots or spinal nerves affected. Dogs usually present
             for vague pelvic limb problems such as trouble rising, reluctance to jump, difficulty climbing stairs,
             lameness, and pain which can be ambiguous. Lameness is reported commonly and may be intermit-
             tent, shifting, unilateral, or bilateral. Regional pain, either occurring spontaneously or detected dur-
             ing physical examination, is common and, occasionally, may be the only historical problem. Care
             should be taken to differentiate discomfort on vertebral extension from hip extension. Applying digi-
             tal pressure over the lumbosacral junction (Figure 20.8 and Video 3.1) and extending the lumbosa-
             cral  junction  by  lifting  the  pelvis  while  pressing  on  the  lumbar  vertebrae  (lordosis  test)  are  two
             specific methods of assessing lumbosacral pain. Extension or traction of the tail and palpation of the
             lumbosacral joint on rectal examination are other methods. Careful assessment of pain responses
             during hip palpation and extension is required to identify coxofemoral disease (Chapter 20). If other
             neurologic deficits such as limb, tail, or anal sphincter paresis are apparent, a tentative diagnosis of
             DLSS can be based on these findings. Fecal and/or urinary incontinence may be historically reported.
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