Page 1117 - Small Animal Internal Medicine, 6th Edition
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CHAPTER 61   Loss of Vision and Pupillary Abnormalities   1089





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                                                                 FIG 61.6
                                                                 Horner syndrome in a domestic short-haired cat with otitis
                                                                 media/interna.



            FIG 61.5                                                    BOX 61.3
            Neoplasm of the optic chiasm identified with magnetic
            resonance imaging in a 7-year-old Doberman Pinscher with   Components of Horner Syndrome
            an acute onset of bilateral blindness and loss of pupillary
            light reflexes but no other neurologic deficits.      Miosis
                                                                  Enophthalmos
                                                                  Ptosis
            neoplasia, congenital  malformations (e.g., hydrocephalus,   Prolapsed nictitans
            lissencephaly), and degenerative disorders (see  Box 60.1).
            Animals with functional disturbances of the forebrain caused
            by metabolic encephalopathies, intoxications, hypoxia, or
            postictal cerebral edema may also present with cortical     BOX 61.4
            blindness that is often transient or intermittent. Diagnostic
            evaluation for cortical blindness should follow the guidelines   Common Causes of Horner Syndrome
            outlined in Chapter 60 for evaluation of animals with sus-
            pected intracranial  disease  and should  include thorough   First-Order (Central) Causes (Rare)
            physical, ophthalmologic, and neurologic examinations; a   Intracranial neoplasia, trauma, infarct, inflammatory
            laboratory  database;  screening  thoracic  and  abdominal   disease
            radiographs and abdominal ultrasound; CSF analysis; and   Cervical spinal cord lesion
            cranial MRI evaluation.                                 Intervertebral disk protrusion
                                                                    Neoplasm
                                                                    Fibrocartilaginous embolism
            HORNER SYNDROME                                         Trauma
                                                                    Infectious inflammatory disease
                                                                    Granulomatous meningoencephalitis
            Lesions disrupting the sympathetic innervation to the eye
            result in Horner syndrome. This condition causes miosis   Second-Order (Preganglionic) Causes
            (constriction of the affected pupil), drooping of the upper   Spinal cord lesion T1-T3 (trauma, neoplasia,
            eyelid (ptosis), and an inward sinking of the eyeball (enoph-  fibrocartilaginous embolism, inflammation)
            thalmos) as well as partial protrusion of the third eyelid   Brachial plexus avulsion
            (nictitating membrane) (Box 61.3; Fig. 61.6).         T1-T3 spinal nerve root tumor
              Horner syndrome can result from injury to the sympa-  Cranial mediastinal mass
            thetic innervation of the eye anywhere along its pathway   Cervical soft-tissue neoplasia, trauma
            (Box 61.4;  Fig. 61.7). Lesions are classified as first  order   Skull base trauma
            (central), second order (preganglionic), or third order (post-  Third-Order (Postganglionic) Causes
            ganglionic) according to the level of the lesion along the   Otitis media/interna
            sympathetic pathway.                                  Neoplasia in middle ear
              First-order neurons originate in the hypothalamus and   Retrobulbar injury, neoplasia
            rostral midbrain and travel down the brainstem and cervical   Idiopathic
            spinal cord to terminate at the preganglionic cell bodies in
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