- •Preface
- •Transient Binocular Visual Loss
- •Migraine with Typical Visual Aura
- •Congenitally Elevated Optic Disc
- •Optic Disc Coloboma
- •Optic Pit
- •Morning Glory Optic Disc Anomaly
- •Optic Disc Hypoplasia
- •Typical Optic Neuritis
- •Atypical Optic Neuritis
- •Arteritic Anterior Ischemic Optic Neuropathy
- •Posterior Ischemic Optic Neuropathy
- •Hypotensive Ischemic Optic Neuropathy
- •Toxic Optic Neuropathy
- •Dominantly Inherited Optic Neuropathy
- •Leber Hereditary Optic Neuropathy
- •Sphenoid Meningioma
- •Optic Nerve Sheath Meningioma
- •Craniopharyngioma
- •Pituitary Adenoma
- •Optic Glioma (Pilocytic Astrocytoma of Optic Nerves or Chiasm)
- •Anterior Visual Pathway Intracranial Aneurysm
- •Traumatic Optic Neuropathy
- •Radiation Optic Neuropathy
- •Graves Optic Neuropathy
- •Papilledema
- •Hypertensive Optic Neuropathy
- •Paraneoplastic Optic Neuropathy
- •Diabetic Papillopathy
- •Homonymous Hemianopia
- •Cerebral (Retrogeniculate, Cortical) Blindness
- •Visual Agnosia
- •Visual Spatial And Attentional Disturbances
- •Orbital Myositis
- •Graves Disease
- •Genetic Extraocular Myopathy
- •Myasthenia Gravis
- •Third Cranial Nerve Palsy
- •Fourth Cranial Nerve Palsy
- •Sixth Cranial Nerve Palsy
- •Unilateral Ophthalmoplegia
- •Bilateral Ophthalmoplegia
- •Direct Carotid–cavernous Fistula
- •Indirect (Dural) Carotid–cavernous Fistula
- •Internuclear Ophthalmoplegia
- •Skew Deviation
- •Dorsal Midbrain (Pretectal) Syndrome
- •Paramedian Thalamic or Midbrain Syndrome
- •Paramedian Pontine Syndrome
- •Dorsolateral Medullary (Wallenberg) Syndrome
- •Acute Upgaze Deviation
- •Acute Downgaze Deviation
- •Omnidirectional Slow Saccades
- •Omnidirectional Saccadic Pursuit
- •Congenital Ocular Motor Apraxia
- •Acute Horizontal Gaze Deviation
- •Ping Pong Gaze
- •Physiologic Nystagmus
- •Congenital Motor Nystagmus
- •Congenital Sensory Nystagmus
- •Monocular Pendular Nystagmus of Childhood
- •Spasmus Nutans
- •Peripheral Vestibular Nystagmus
- •Acquired Binocular Pendular Nystagmus
- •Sidebeat, Upbeat, and Downbeat Nystagmus
- •Epileptic Nystagmus
- •Convergence–retraction “Nystagmus”
- •Voluntary “Nystagmus”
- •Superior Oblique Myokymia
- •Square Wave Jerks
- •Ocular Flutter and Opsoclonus
- •Ocular Dysmetria
- •Ocular Bobbing
- •Tonic Pupil
- •Argyll Robertson Pupils
- •Tectal (Dorsal Midbrain) Pupils
- •Pharmacologically Dilated Pupil
- •Mydriatic Pupil of Third Cranial Nerve Palsy
- •Mydriatic Pupil of Traumatic Iridoplegia
- •Episodic Pupil Dilation
- •Horner Syndrome
- •Ptosis
- •Lid Retraction
- •Apraxia of Eyelid Opening
- •Benign Essential Blepharospasm
- •Hemifacial Spasm
- •Index
• 12 SECTION Disorders Pupil
Horner Syndrome
Key Facts
•Miosis and ipsilateral ptosis
•Caused by sympathetic denervation
•Lesion may lie within the first (central), second (preganglionic), or third (postganglionic) segment of oculosympathetic pathway
•Causes of postganglionic Horner syndrome:
•cervical carotid dissection
•surgery, trauma, or mass in neck
•cavernous sinus lesion
•cluster headache
•idiopathic
•Causes of preganglionic Horner syndrome in children:
•birth injury
•neuroblastoma
•Causes of preganglionic Horner syndrome in adults:
•surgery, trauma, or mass in paraspinal, neck, or apical lung regions
•Causes of central Horner syndrome:
•dorsolateral medullary infarction (Wallenberg syndrome)
•cervicothoracic cord syrinx, trauma, or tumor
Clinical Findings
•Anisocoria in dim light with normal pupil constriction to bright light
•Ptosis ipsilateral to smaller pupil
•Anisocoria rarely >2 mm
•Dilation lag of affected pupil
•Ptosis, never >3 mm, need not be present
•Ipsilateral elevation of lower lid (upside down ptosis) sometimes
•Ipsilateral conjunctival injection sometimes
•Ipsilateral facial anhydrosis (central or preganglionic lesions)
Ancillary Testing
•30 min after instillation of cocaine 10%, residual anisocoria should be >1 mm
•Apraclonidine 0.5% should eliminate anisocoria or cause reversal of anisocoria (small pupil becomes larger pupil)
•MRI or magnetic resonance angiography should extend from skull vertex to midthoracic region regardless of results of topical pharmacologic pupil tests
• use dedicated ‘carotid dissection’ protocol if Horner syndrome is acute
Differential Diagnosis
•Ptosis from trauma, senescence, or myasthenia gravis
•Miosis from physiologic anisocoria or iris pathology
224
A
B
C
Fig. 12.10 Right Horner syndrome. (A) In dim illumination, left pupil is larger than right pupil. (B) In brightness, both pupils constrict normally. (C) After instillation of 10% cocaine, right pupil dilates less than left pupil.
A B
Fig. 12.11 Right internal carotid artery dissection.
(A) Precontrast axial T1 shows a white crescent around the right internal carotid artery at a high cervical level, indicating a blood clot dissected within the vessel wall (arrow). (B) Maximum intensity projection magnetic resonance angiography of the neck vessels shows that the lumen of the right internal carotid artery lumen is narrowed (arrowheads) compared with the normal caliber left carotid artery (arrow).
Syndrome Horner
225
Horner Syndrome (Continued)
Treatment
• Depends on underlying lesion
• Apraclonidine 0.5% for ptosis
Prognosis
• Depends on underlying lesion
• Even if ophthalmic manifestations do not remit, symptoms are non-disabling
•If ptosis is a cosmetic blemish, can treat with daily instillation of apraclonidine 0.5% or with eyelid surgery
• 12 SECTION Disorders Pupil
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Fig. 12.12 Thoracic neuroblastoma causing Horner syndrome. Axial chest CT shows a large mass (arrow) in a 3 year-old child presenting with an isolated Horner syndrome.
(continued) Syndrome Horner
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Section |
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13 |
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Eyelid Disorders |
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Ptosis |
230 |
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Lid Retraction |
232 |
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Apraxia of Eyelid Opening |
234 |
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Benign Essential Blepharospasm |
236 |
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Hemifacial Spasm |
238 |
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