Page 806 - Clinical Small Animal Internal Medicine
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Table 71.1  Clinical signs of forebrain disease
             Clinical sign   Notes

             Seizures        Can occur with lesions in the cerebral hemispheres, thalamus or hypothalamus
  VetBooks.ir  Propulsive walking  Patients with forebrain disease circle towards the side of the lesion, but without signs of vestibular disease
             Circling
                             (no head tilt or nystagmus present)
             Head pressing
             Obtundation     Obtundation describes decreased responsiveness to normal stimuli. This is often a sign of bilaterally
                             symmetric, global cerebral hemisphere disturbance. Further disturbance of level of consciousness (i.e., stupor
                             or coma) is more likely to signify the presence of a brainstem lesion
             Contralateral cortical  Absent menace response (as a result of absent vision) with normal consensual and indirect pupillary light reflex
             blindness       occurs as a result of lesions in the occipital cortex or affecting the internal capsule, caudal to the level of the
                             lateral geniculate nucleus, on the side opposite the affected eye
             Proprioceptive   Patients with forebrain disease often have a relatively normal gait but significant proprioceptive deficits that are
             deficits        only evident on testing or on negotiating stairs or other difficult terrain
             Decerebrate rigidity  Decerebrate rigidity (increased extensor tone in all four limbs with opisthotonus) indicates severe, bilateral
                             forebrain disease and is a reflection of functional disconnection of the cerebral peduncles from the brainstem
             Hemi‐inattention   This occurs rarely as a result of lesions affecting the sensory cortex and is most commonly evident while eating.
             syndrome        Patients with hemi‐inattention syndrome will eat one half of a bowl of food, apparently ignoring the other half unless
                             it is rotated 180°. The lesion is situated within the cerebral hemisphere contralateral to the “ignored” side of the body
             Behavioral/memory   The most commonly noted behavioral and memory changes seen in patients with forebrain disease include loss
             changes         of toilet training, loss of recognition of family members or toys, and changes in personality
             Vestibular signs  Lesions in the thalamus will rarely produce vestibular signs. This is most commonly reported in patients with
                             cerebrovascular accidents


             Box 71.1  Differential diagnoses for forebrain disease according to underlying etiology
             Degenerative               Lysosomal storage diseases
                                        L2‐hydroxyglutaric aciduria in Staffordshire terriers
             Anomalous                  Hydrocephalus
                                        Lissencephaly
                                        Porencephaly
                                        Hydranencephaly
                                        Meningoencephalocele (Dandy‐Walker syndrome)
             Metabolic                  Hepatic encephalopathy
                                        Renal (uremic) encephalopathy
                                        Hypoglycemia
                                        Electrolyte abnormalities: hypo/hypernatremia
                                        Hypothyroid myxedema coma
             Neoplastic                 Meningiomas
                                        Glial tumors:
                                          Oligodendrogliomas
                                          Astrocytomas
                                        Ependymomas
                                        Choroid plexus tumors
                                        Pituitary tumors
                                        Metastatic disease
                                        Lymphosarcoma
             Nutritional                Thiamine deficiency
             Infectious/inflammatory    Viral: distemper, feline infectious peritonitis, rabies, Borna disease virus
                                        Protozoal: Toxoplasma, Neospora
                                        Fungal: Cryptococcus, Aspergillus, blastomycosis, others (pheohyphomycotic encephalitis)
                                        Rickettsial: Rocky Mountain spotted fever, Ehrlichia
                                        Bacterial: abscess; meningitis
                                        Parasitic: Cuterebra, verminous encephalitis
             Inflammatory (noninfectious)  Granulomatous meningomyeloencephalitis
                                        Necrotizing encephalitides
             Idiopathic                 Idiopathic epilepsy
             Toxins                     Lead
                                        Organophosphate
                                        Metronidazole
                                        Cyanide, sodium fluoroacetate, hydrocarbons, other heavy metals
             Vascular                   Hemorrhagic and ischemic infarcts
                                        Feline ischemic encephalopathy
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