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Vascular neuro-ophthalmology includes visual symptoms and signs found in stroke patients as well as numerous primary vascular disorders involving the eye and the optic nerves. The clinical presentation varies depending on the type of vessel involved (arteries versus veins), the type of stroke (ischemic or hemorrhagic), and the size of the arteries involved (large versus small artery disease).
The blood supply to the eye is mostly provided by branches of the ophthalmic artery, which is a branch of the internal carotid artery (ICA) (Fig. 1A). This is why many patients with cerebral ischemia in the territory of the anterior circulation may present with ipsilateral visual changes. The posterior circulation provides the blood supply to the occipital lobes and posterior fossa; hence binocular visual loss or abnormal extraocular movements are common with vascular diseases affecting the posterior circulation. In addition, a number of ocular vascular disorders are associated with specific neurologic manifestations and numerous systemic inflammatory diseases or hypercoaguable states can affect the eyes and the brain simultaneously.
Anterior and posterior large-artery circulation ischemia is often associated with visual symptoms and signs which may precede a cerebral infarction.
A variety of transient and permanent visual symptoms and signs may develop in patients with carotid artery disease. The hallmark of most of these disturbances is their monocular nature, ispilateral to the affected ICA. However, contralateral homonymous visual field defects, bitemporal visual field defects, and bilateral simultaneous visual loss may result from diseased carotid arteries and their branches, particularly when the disease is bilateral.
This is the most common ophthalmologic symptom of disease of the ICA. The term “amaurosis fugax” is often used to describe any cause of transient monocular visual loss and should be abandoned . The evaluation and management of patients with transient visual loss are detailed in chapter 3. It is important to emphasize that there are numerous nonvascular causes of transient monocular visual loss which require an emergent detailed ocular examination; therefore an ophthalmic consultation should be obtained before launching an extensive work up for presumed vascular transient monocular visual loss . Multiple episodes of transient visual loss or painful transient visual loss in the elderly should raise the possibility of giant cell arteritis.
Partial or complete monocular loss of vision may occur in patients with carotid artery disease, usually in the ipsilateral eye. This results most often from a central retinal artery occlusion (CRAO) or from one or multiple branch retinal artery occlusions (BRAO). In such cases, an embolus may be seen in the affected vessels. Other causes of permanent monocular visual loss in patients with carotid artery disease include venous stasis retinopathy, and the ocular ischemic syndrome . Ischemic optic neuropathy, anterior or posterior, results from small vessel disease (Fig. 1B) and is usually not associated with large artery disease , explaining why carotid artery evaluation is not usually indicated in patients with classic anterior ischemic optic neuropathy.
The second major visual sign of carotid occlusive disease is a partial or complete contralateral homonymous hemianopic visual field defect. This is most often caused by occlusion of branches of the middle cerebral artery, but it may result from occlusion of the anterior choroidal artery or some of its branches to the optic tract and lateral geniculate body. Rarely, patients with carotid occlusive disease have severe visual deficits caused by a combination of monocular visual loss from ocular circulation insufficiency and contralateral homonymous field loss from damage to the ipsilateral post-chiasmal visual sensory pathway.
Patients who experience a retinal infarction usually complain of acute loss of visual acuity, visual field, or both. Permanent visual loss may be preceded by episodes of transient monocular visual loss. Patients with a CRAO almost always have extremely poor visual acuity in the affected eye. Acute CRAO is characterized by diffuse pale swelling of the retina, a macular “cherry red” spot, and attenuation of the retinal vessels (Fig. 2) . Within a few weeks, the retinal vessels often recanalize and the retina has an almost normal appearance; however, the optic disc becomes pale (Fig. 3) . Emboli are seen in up to 40% of central retinal artery occlusions and in a majority of branch artery occlusions (Fig. 4) [5,6,7]. The most common emboli that occlude retinal arterioles are made of cholesterol, fibrin-platelets, and calcium fragments (Table 1).
Carotid artery disease is responsible for the majority of retinal infarctions. In patients with embolic retinal infarction who have a normal ICA, the aortic arch or the heart are the most likely sources of emboli (8). The prognosis of CRAO is poor and treatment is limited. None of the “classic” treatments often offered by ophthalmologists (including ocular massage, anterior chamber paracenthesis, etc…) are proven to be useful and we do not recommend them routinely. Selective intra-arterial thrombolysis (directly into the ophthalmic artery) or intra-venous thrombolysis are sometimes performed in specialized centers, but remain debated until a clinical trial shows their efficacy and safety [9,10].
Ophthalmic artery occlusion usually results from large emboli in the ophthalmic artery. The visual loss is profound and the prognosis poor. Funduscopic examination shows extensive retinal ischemia which appears white and edematous, often with hemorrhages and with poor or no retinal artery filling, as well as disc edema. Since the choroidal circulation is also compromised, there is no “cherry red” spot (Fig. 5).
Ischemia in the anterior circulation (carotid territory) may be associated with a contralateral homonymous hemianopia when there is a lesion of the optic tract, lateral geniculate body, or anterior optic radiations.
Damage to the optic tract produces a contralateral homonymous hemianopia associated with a relative afferent pupillary defect on the side of the hemianopia, and subsequent optic nerve atrophy (because the axons of the optic tract originate in the ganglion cell bodies of the retina) .Lesions of the lateral geniculate body may produce a homonymous sectoranopia because of its unique blood supply. Lesions of the anterior optic radiations typically produce a contralateral homonymous hemianopia, usually in association with other neurologic symptoms or signs .
Venous stasis retinopathy — also called hypotensive retinopathy — is caused by severe carotid obstructive disease and poor collateral circulation. The retinopathy is characterized by insidious onset, dilated and tortuous retinal veins, peripheral microaneurysms, and dot-blot hemorrhages in the midperipheral retina (Fig. 6). Patients with this condition complain primarily of generalized blurred vision in the affected eye or may be asymptomatic. Symptoms of carotid insufficiency, such as transient monocular visual loss, decreased vision after exposure to bright light, and orbital pain are common. Venous stasis retinopathy may occur as part of the ocular ischemic syndrome or in isolation. It is found in up to 4-18% of patients with carotid occlusive disease, and is often asymptomatic [12,13,14]. Venous stasis retinopathy usually resolves spontaneously if arterial patency can be restored . In many cases, however, there is persistent visual dysfunction from irreversible retinal ischemic changes. If ocular perfusion cannot be improved, the affected eye may develop neovascularization of the iris and optic disc as well as other signs of ocular ischemia. In such cases, ablation of hypoxic retinal tissue by panretinal photocoagulation may prevent progression of the condition and may actually produce regression of neovascularization [14,15].
The ocular ischemic syndrome (also called ischemic ocular inflammation or chronic ocular ischemia) is a progressive disorder resulting from chronic hypoperfusion of the eye [14,16]. Patients describe blurry vision that may be transient or persistent. Visual loss is typically insidious and slowly progressive. Some patients describe positive after-images when exposed to bright light. The affected eye is often red, with episcleral vascular dilation . The ocular fundus shows venous stasis retinopathy , sometimes associated with neovascularization. Some patients will have severe ocular or peri-orbital pain which is often improved when they lie down . In eyes with persistent hypoperfusion, neovascularization of the iris, retina, optic disc, and anterior chamber angle develop. Other signs of ocular ischemia include corneal edema, uveitis, cataract formation, and a dilated and poorly reactive pupil . The visual prognosis is extremely poor. Although early retinopathy may resolve spontaneously with the development of collateral circulation, severe loss of vision is almost always irreversible once tissue infarction occurs [14,15].
The treatment of the ocular ischemic syndrome is aimed at preservation and improvement of visual function and treatment of the underlying process [14,15]. The first requires a relative decrease in the oxygen requirements of the eye, thus reducing the drive for neovascularization. This is usually accomplished by ablation of retinal tissue by laser panretinal photocoagulation or peripheral retinal cryotherapy. When severe carotid artery stenosis is the underlying condition, endarterectomy or carotid stenting may be used to re-establish flow. When, as is usually the case, the artery is occluded, a superficial temporal artery to middle cerebral artery bypass procedure may be beneficial if the external carotid artery is patent. When the internal and external carotid arteries are occluded, some form of revascularization of the external carotid artery may be of some benefit. However, revascularization procedures have been associated with ocular complications such as retinal or vitreal hemorrhages and elevated intraocular pressure. Moreover, patients with such severe carotid disease and poor collateral circulation often have a high surgical risk. No therapy is clearly effective in reversing the ocular ischemic syndrome.
Although it is more common in carotid artery dissections, Horner syndrome may occur in patients with atherosclerotic carotid artery disease (Fig. 7) . Most such patients have complete occlusion of the ICA, and the Horner syndrome is associated with other neurological symptoms and signs of carotid artery disease. Horner syndrome occurring in patients with occlusion of the internal carotid artery is almost always postganglionic (third order) (see chapter 7).
Exceptionally, patients with acute occlusion or severe ICA stenosis may develop one or more ocular motor nerve pareses on the side of the occlusion, either in isolation or with signs of ocular ischemia . In some cases of isolated ocular motor nerve palsy, ischemia of the nerve probably results from reduction of blood flow through mesencephalic branches of the anterior choroidal artery. In other cases, blood supply to the cranial nerves themselves, which originates from branches of the ICA, may be compromised [3,19].
Isolated ocular pain may be a symptom of carotid occlusive disease, even without other symptoms and signs of vascular disease. It is usually a referred pain resulting from ischemia or compression of the trigeminal branches. It may also be part of the ocular ischemic syndrome .
The vertebrobasilar system supports the neural components of the entire brainstem ocular motor system as well as those of the posterior visual sensory pathways and visual cortex. For this reason, ocular motor and visual symptoms and signs play a major role in the diagnosis of vascular disease in the vertebrobasilar system.
Episodes of transient binocular visual loss are common in vertebrobasilar ischemia. The visual loss is always bilateral, with both eyes being affected simultaneously and symmetrically [3,20.21,22]. The change in vision may be described as a sudden “grayout of vision,” “a sensation of looking through fog or smoke,” or “the feeling that someone has turned down the lights.” Most attacks of blurred vision that result from vertebrobasilar ischemia last less than a minute. Attacks of longer duration may be accompanied by flickering, flashing “stars” of silvery light in a homonymous or altitudinal field of vision. They may occur alone or in combination with other transient symptoms in the vertebrobasilar territory. The episodes of blurred vision that occur in patients with occipital ischemia must be differentiated from other causes of transient or permanent visual loss. Transient, complete 90-180° inversion of the visual image occasionally occurs.
An isolated homonymous visual field defect of sudden onset is the hallmark of a vascular lesion in the occipital lobe (Fig. 8). Such a lesion is usually the result of infarction in the territory supplied by the posterior cerebral artery (PCA) (Table 2). The field defect may be complete or incomplete, but when it is incomplete or scotomatous, it is usually congruous. When there is a complete homonymous hemianopia, macular sparing is common, and the occipital pole is usually spared. Patients with a homonymous visual field defect caused by ischemia in the PCA territory have normal visual acuity. When both occipital lobes are infarcted, visual acuity is usually severely impaired but the amount of visual loss is symmetric in both eyes (Fig. 9). In some cases of occipital lobe infarction, the anterior portion of the lobe is unaffected, resulting in sparing of part or all of the peripheral 30° of the contralateral, monocular temporal field — the temporal crescent. Symptoms of PCA occlusion usually occur without warning. The patient may have a slight sensation of dizziness or light-headedness and then become aware of a homonymous visual field defect. Some patients initially experience complete blindness, with vision returning in the ipsilateral homonymous visual field within minutes. Pain in the ipsilateral eye or over the ipsilateral brow (contralateral to the hemianopia) is an important although inconstant symptom in such patients . This pain is referred from the tentorial branches of the trigeminal nerve.
Alexia without agraphia results from infarction of the left occipital lobe and disruption of the left ventral visual association cortex and its outflow tracts to the left angular gyrus, thus interrupting input from the right occipital area to the language verbal association area. Patients can usually name individual letters or numbers, but they cannot read words or phrases. Although they are able to write, they cannot read it back moments later. Patients in whom there is infarction of the left occipital lobe and the splenium of the corpus callosum have no visual information to send to the language center from the left occipital lobe, and information from the right occipital lobe cannot be transmitted across to the left language center via the corpus callosum.
Gerstmann syndrome results from infarction of the left angular gyrus secondary to an occlusion of the left PCA. Patients have difficulty telling right from left, difficulty in naming digits on the patient’s own or another’s hand, constructional dyspraxia, agraphia, and difficulty calculating.
Associative visual agnosia is present in some patients with a left PCA occlusion. It consists of difficulty understanding the nature and use of objects presented visually. However, they can trace with fingers, and they can copy an object presented in the hand and explored by touch or verbally described by the examiner.
Prosopagnosia results from occlusion of the right PCA. Patients with this condition have difficulty recognizing familiar faces. The patients may also have difficulty revisualizing to themselves what a given object or person should look like, and their dreams are often devoid of visual imagery.
Visual neglect is much more common after occlusion of the right posterior cerebral artery with infarction of the right parietal lobe than it is after occlusion of the left posterior cerebral artery.
Cerebral blindness occurs with bilateral PCA occlusions. Patients with this syndrome may have premonitory episodes of bilateral visual blurring or focal brainstem ischemia before they develop acute, bilateral, simultaneous visual loss caused by bilateral simultaneous homonymous hemianopia. Many cases of cortical blindness are caused by basilar artery thrombosis. The pupils and fundus examination are normal. Many of the patients experience photopsias or formed visual hallucinations while they are totally blind. Denial of blindness, known as Anton’s syndrome, is common. Bilateral occipital lobe infarction can produce decreased central visual acuity in both eyes without any obvious hemianopic defect. The loss of central vision probably results from generalized ischemia of the occipital lobes and is symmetric in both eyes, unless there is an associated unilateral or asymmetric ocular disease.
Balint’s syndrome can occur in patients who experience bilateral simultaneous or sequential PCA occlusions, although it is most common after bilateral watershed infarctions between the PCA and MCA territories, primarily damaging the parieto-occipital visual associative areas. Balint’s syndrome occurs much more frequently after bilateral watershed infarctions of the parieto-occipital regions from systemic hypotension than from thrombo-embolic carotid or vertebrobasilar disease. Patients with this syndrome present with a triad of “psychic paralysis of visual fixation,” “optic ataxia,” and visuospatial disorientation. Patients with Balint’s syndrome have a variety of abnormalities of fixation and tracking. They have great difficulty locating a stationary object in space, although they can maintain fixation on the object once they locate it. They can track a moving target, but if the target begins to move rapidly, it is lost and cannot be relocated.
Simultagnosia may develop in patients with bilateral superior occipital lobe strokes. Such patients complain of piecemeal perception of the visual environment wherein objects may look fragmented or even appear to vanish from direct view. Simultagnosia is caused by a defect in visual attention that results in an inability to sustain visuospatial processing across simultaneous elements in an array. Simultagnosia, like Balint’s syndrome and other higher disorders of visual processing and attention, occurs much more frequently after systemic hypotension with watershed infarctions than from occlusion of the PCAs. Common causes include cardiac arrest and intraoperative hypotension.
Achromatopsia occurs in association with prosopagnosia when occipital lobe infarction is limited to the lower banks of the calcarine fissures on both sides.
Formed visual hallucinations may be produced by vertebrobasilar ischemia. These hallucinations, which may last 30 minutes or more, may be associated with decreased consciousness, but they usually occur in an otherwise alert patient who is aware that the visual images are not real. The hallucinations are generally restricted to a hemianopic field, and they are often complex. Some of the visual hallucinations that occur in patients with posterior cerebral artery occlusion are palinoptic, with the hallucinations consisting of recently or previously seen images .
Transient binocular horizontal or vertical diplopia is a common manifestation of vertebrobasilar ischemia. The diplopia may result from transient ischemia of the ocular motor nerves or their nuclei (ocular motor nerve paresis) or from transient ischemia to supranuclear or intemuclear ocular motor pathways (skew deviation, internuclear ophthalmoplegia, gaze paresis). In most cases, the diplopia is not isolated and the patient has other neurologic symptoms suggesting vertebrobasilar ischemia [24,25,26,27,28,29].
Persistent disturbances of eye movements are extremely common in patients with vertebrobasilar ischemia. Ocular motor nerve paresis, internuclear ophthalmoplegia, supranuclear deficits and nystagmus develop based on the anatomical location of the lesion. Nystagmus produces oscillopsia which is often described by the patients as ““jumping of vision.”
Both infectious and noninfectious inflammation affecting the central nervous system can produce visual symptoms. In some vasculitides with a predilection for large arteries, such as Takayasu’s arteritis, ocular ischemia is common. Most often, vasculitis produces retinal vasculitis with retinal vascular occlusions and visual loss, often associated with ocular inflammation (uveitis) (Fig. 10) .
Giant cell arteritis should be considered in all patients over 50 years-old presenting with acute optic nerve or retinal ischemia . Permanent visual loss is common in giant cell arteritis, and is often preceded by transient monocular visual loss (see chapter 8).
Susac syndrome describes young patients with multiple bilateral branch retinal arterial occlusions, hearing loss, and neurologic symptoms suggestive of a brain microangiopathy . It classically occurs in young women but can affect men. Affected patients have recurrent multiple branch retinal occlusions that are most often bilateral, progressive hearing loss, and various neurologic presentations including psychiatric changes and encephalopathy. The disease usually has a chronic relapsing course punctuated by frequent remissions and exacerbations .
Retinal fluorescein angiography classically shows retinal arterial wall hyperfluorescence, which is indicative of disease activity (Fig.11) Hearing loss primarily involves low and medium frequencies, and is best demonstrated by audiogram. It is believed to result from cochlear damage caused by occlusions of the cochlear end arterioles. Encephalopathy varies in severity from mild memory loss and personality changes to severe cognitive dysfunction, confusion, psychiatric disorders, seizures, and focal neurologic symptoms and signs. The brain involvement in Susac syndrome is usually the most severe part of the disease and is frequently very debilitating.
Electroencephalograms usually show diffuse slowing. Cerebrospinal fluid examination may be normal or show a variable degree of leukocytosis (lymphocytes), with elevation of protein. The neuroimaging modality of choice is the brain MRI, which typically shows multiple enhancing small lesions in both the white and gray matter, with classic involvement of the corpus callosum (an otherwise unusual location for vascular disease) . The MRA is normal, but catheter angiography has shown evidence of vasculopathy in some patients. In a few cases, brain biopsy was performed and showed microinfarcts with some minimal perivascular lymphocytic infiltration, but no true vasculitis.
Because of the spontaneously remitting—relapsing course of Susac syndrome, and the small number of cases reported, it is difficult to assess the efficacy of the various treatments that have been tried. Most patients receive steroids, immunosuppressive agents, and antiplatelet/antithrombotic therapy until the disease becomes clinically inactive [31,33].
A number of rare hereditary retinopathies are associated with central nervous system abnormalities. Recent genetic characterization of three of these syndromes has shown that there is an overlap among these entities (Table 3) .
A variety of other systemic disorders producing strokes may be associated with ocular abnormalities (Table 4). Most are inherited disorders, and ophthalmic manifestations may reveal the angiopathy [3,11].
Patients with systemic hypertension may develop a severe encephalopathy often associated with reversible visual loss (also called posterior reversible encephalopathy syndrome) (Fig. 9) [35,36]. Hypertensive retinopathy may also be present bilaterally and does not always correlate with the severity of the hypertensive encephalopathy. There may be associated optic nerve head edema which may mimic that of raised intracranial pressure (Fig. 12).
Most vascular diseases involving the optic nerve fall under the category of anterior and posterior ischemic optic neuropathies believed to be small vessel diseases . These entities are discussed in chapter 5.
Several studies have shown that retinal microvascular changes are related to clinical stroke, stroke mortality, coronary artery disease, cognitive changes, cerebral white matter changes detected by MRI, and cerebral atrophy [37,38,39,40]. In these studies, retinal vascular changes (generalized and focal narrowing of the retinal arterioles, arteriovenous nicking, micro- aneurysms) and retinopathy (cotton wool spots, retinal hemorrhages) were evaluated on fundus photographs [37,38,39,40].
The most common neuro-ophthalmic manifestations of intracranial aneurysms are secondary to a local mass effect on adjacent cranial nerves. The pulsatile process of the aneurysm may be as important as the direct mass effect . Manifestations of the aneurysm depend on its location and its size. Aneurysms arising from the ophthalmic artery, the cavernous carotid artery, the anterior communicating artery, or the internal carotid artery can result in unilateral optic neuropathy or chiasmal visual field defects . Rarely, a homonymous hemianopia can result from compression of the optic tract. Multiple ocular nerve palsies can result from an aneurysm involving the cavernous carotid artery. Posterior communicating artery aneurysms classically produce an isolated third nerve palsy, whereas isolated trochlear or abducens nerve palsies only rarely result from aneurysmal compression (see chapter 1) .
Aneurysmal rupture producing a subarachnoid hemorrhage may be associated with retinal, subhyaloid, and vitreal hemorrhages in one or both eyes (so called “Terson syndrome”) (Fig. 13). The presumed mechanism is that of acute raised intracranial pressure with sudden elevation of ocular central venous pressure. Vision loss is variable but is not associated with a relative afferent pupillary defect unless the retina is detached. The diagnosis is often delayed in ICU patients who may not be aware of visual loss. Unless there is an associated retinal detachment, treatment is usually deferred and a vitrectomy is performed only if the hemorrhage does not resolve spontaneously [42,43].
When an aneurysm arises from the cavernous carotid artery or from its branches in the cavernous sinus, rupture results in carotid-cavernous fistula, not subarachnoid hemorrhage.
Direct carotid-cavernous fistula results from direct communication of the cavernous carotid artery and the cavernous sinus with resultant high velocity of blood flow . Direct carotid-cavernous fistulas can result from trauma or from rupture of a preexisting aneurysm of the cavernous carotid artery. Ocular manifestations are usually obvious and include proptosis, periorbital swelling, chemosis, dilation of the episcleral vessels, orbital bruit, ophthalmoplegia, elevated intraocular pressure, dilation or occlusion of the retinal veins and optic disc edema .
Dural carotid-cavernous sinus fistulas result from indirect communications between branches of the internal and external carotid arteries and the cavernous sinus. They are more common in middle aged and elderly woman. Neuro-ophthalmic manifestations depend on the blood flow velocity and vary from the full classical appearance of direct fistulas to isolated bruit, cranial nerve palsies, or simply a “red eye” (Fig. 14). Their diagnosis is therefore more difficult and is often delayed.
Orbital imaging with CT or MRI classically shows dilatation of the superior ophthalmic veins, enlargement of the extra-ocular muscles, or enlargement of the cavernous sinus (Fig. 14). Catheter angiography is still the best way to confirm a carotid cavernous fistula which can often be treated with an endovascular approach at the same time.
Intracranial arteriovenous malformations may result in intraparenchymal hemorrhage, subarachnoid hemorrhage, seizures, or mass effect [46,47]. Occipital arteriovenous malformations can cause episodic visual symptoms mimicking the visual aura of migraine. Homonymous hemianopia is common in occipital lesions, most often as the result of bleeding or as a complication of treatment (Fig. 15). Posterior fossa arteriovenous malformations usually cause intermittent or permanent diplopia, often associated with other neurological signs. Orbital arteriovenous malformations produce an acute or subacute orbital syndrome, including proptosis, chemosis, ophthalmoplegia, visual loss, and elevation of the intraocular pressure.
Retinal arteriovenous malformations are rare. They are sometimes isolated or are associated with intracranial or facial arteriovenous malformations .
Cavernous hemangiomas are most common in the posterior fossa and usually produce diplopia when they bleed . Familial cavernous hemangiomas are often multiple and may be associated with grape-like appearing small retinal hemangiomas which are usually asymptomatic (Fig. 16).
Central retinal vein occlusion (CRVO) is a common ocular disorder in elderly patients, often associated with atheromatous vascular risk factors . Occlusion of the central retinal vein is presumed to result from compression by the central retinal artery within the optic nerve. Central retinal vein occlusion is also the most common ocular vascular occlusion associated with hypercoaguable states, whereas central retinal artery occlusion and ischemic optic neuropathy are very rarely associated with hypercoaguable states. Patients with CRVO complain of blurry vision, the severity of which depends on the severity of the CRVO and associated retinal ischemia. Funduscopic examination reveals diffusely spread retinal superficial hemorrhages, retinal and macular edema, dilated and tortuous veins, and optic disc edema (Fig. 17). Cotton-wool spots suggest associated retinal ischemia, indicating a worse visual prognosis. Neovascularization of the retina, optic disc, and iris predisposes the patient to intravitreous hemorrhage, traction retinal detachment and neovascular glaucoma. This disorder is primarily managed by the ophthalmologist and the goals of the treatment are to treat macular edema and prevent or treat neovascularization and its complications .
Branch retinal vein occlusions (BRVO) result from direct compression from a retinal branch artery sharing a common sheath at an arterio-venous crossing (Fig 18). The signs of vein occlusion are limited to the retinal area drained by the occluded branch vein. Vision loss depends on the localization of the occluded vein branch and the involvement or sparing of the macula; prognosis is usually much better than for CRVO .
Cerebral infarction related to cerebral venous thrombosis may present with acute focal neurological signs, including homonymous hemianopia or cranial nerve palsies, usually in the setting of headaches or altered mental status [52,53]. Most neuro-ophthalmic manifestations of cerebral venous thrombosis, however, are related to increased intracranial pressure , and include papilledema and diplopia from uni- or bilateral sixth nerve palsies (Fig. 19). Diagnosis and management of cerebral venous thrombosis are detailed in chapter 2.
Cavernous sinus thrombosis is extremely rare and produces acute painful proptosis with chemosis, ophthalmoplegia, venous stasis retinopathy and visual loss .
Cerebrovascular diseases are commonly associated with neuro-ophthalmologic symptoms or signs, which mostly depend on the type, the size and the location of the vessels involved, and the mechanism of the vascular lesion. Funduscopic examination allows direct visualization of the retinal circulation which shares many common characteristics with the cerebral microcirculation, and can be used as a marker of vascular disease
This work was supported in part by a departmental grant (Department of Ophthalmology) from Research to Prevent Blindness, Inc, New York, New York, and by core grant P30-EY06360 (Department of Ophthalmology) from the National Institute of Health, Bethesda, Maryland. Dr Newman is a recipient of a Research to Prevent Blindness Lew R. Wasserman Merit Award. Dr Lamirel is supported by Research Grants from Institut Servier (Paris, France), Fondation Planiol (Varennes, France) and the Philippe Foundation Inc. (New York, USA)