- •Preface
- •1: Anatomy and Physiology of the Retina
- •Pars Plana
- •Ora Serrata
- •Macula
- •Fovea, Foveola, and Umbo
- •Neurosensory Retina
- •Photoreceptors
- •Retinal Pigment Epithelium
- •Retinal Blood Flow
- •Choroid
- •Vitreous
- •Normal Retinal Adhesion
- •Blood-Retinal Barrier
- •Physiology of the Retina
- •Clinical Correlation: Retina
- •Clinical Correlation: Retinal Pigment Epithelium
- •Clinical Correlation: Vitreous, Retinal Adhesion, and Blood-Retinal Barrier
- •2: Ancillary Testing for Retinal and Choroidal Diseases
- •Fluorescein Angiography
- •Fluorescein Angiography: Hyperfluorescence
- •Fluorescein Angiography: Hypofluorescence
- •Indocyanine Green Angiography
- •Electroretinography
- •Electro-Oculography
- •Echography
- •Scanning Laser Ophthalmoscopy
- •Optical Coherence Tomography
- •3: Clinical Features of Retinal Disease
- •Cherry Red Spot
- •Chorioretinal Folds
- •Choroidal Neovascularization
- •Cotton Wool Spot
- •Cystoid Macular Edema
- •Drusen
- •Flecked Retina Syndromes
- •Foveal Yellow Spot
- •Intraretinal Hemorrhages
- •Lipid Exudates
- •Macular Atrophy
- •Optic Disc Edema With Macular Star
- •Peripheral Pigmentation
- •Pigmented Lesions
- •Preretinal Hemorrhage
- •Retinal Crystals
- •Retinal Neovascularization
- •Retinitis
- •Rubeosis
- •Tumors
- •Vasculitis
- •Vitelliform Lesions
- •Vitreous Hemorrhage
- •Vitreous Opacity
- •White Dot Syndromes
- •White-Centered Retinal Hemorrhages
- •4: Macular Diseases
- •Age-Related Macular Degeneration: Nonexudative
- •Age-Related Macular Degeneration: Exudative
- •Angioid Streaks
- •Central Serous Chorioretinopathy
- •Cystoid Macular Edema
- •Macular Hole
- •Myopic Degeneration
- •Pattern Dystrophy
- •Photic Retinopathy
- •5: Retinal Vascular Diseases
- •Branch Retinal Artery Occlusion
- •Branch Retinal Vein Occlusion
- •Central Retinal Artery Occlusion
- •Central Retinal Vein Occlusion
- •Hypertensive Retinopathy
- •Idiopathic Juxtafoveolar Retinal Telangiectasis
- •Leukemic Retinopathy
- •Ocular Ischemic Syndrome
- •Pregnancy-Related Retinal Disease
- •Radiation Retinopathy
- •Retinal Arterial Macroaneurysms
- •Retinopathy of Prematurity
- •Sickle Cell Retinopathy
- •6: Hereditary Retinal Disorders
- •Albinism
- •Choroideremia
- •Cone Dystrophies/Cone-Rod Dystrophies
- •Congenital Stationary Night Blindness
- •Dominant Drusen
- •North Carolina Macular Dystrophy
- •Retinitis Pigmentosa (Rod-Cone Dystrophies)
- •Stargardt Disease
- •7: Drug Toxicities
- •Aminoglycoside Toxicity
- •Crystalline Retinopathies
- •Iron Toxicity
- •Phenothiazine Toxicity
- •8: Intraocular Tumors
- •Choroidal Hemangioma
- •Choroidal Melanoma
- •Choroidal Metastasis
- •Choroidal Nevus
- •Choroidal Osteoma
- •Congenital Hypertrophy of the Retinal Pigment Epithelium
- •Intraocular Lymphoma
- •Melanocytoma
- •Phakomatoses: Neurofibromatosis
- •Phakomatoses: Sturge-Weber Syndrome
- •Phakomatoses: Tuberous Sclerosis
- •Phakomatoses: Von Hippel-Lindau Disease
- •Phakomatoses: Wyburn-Mason Syndrome
- •Retinoblastoma
- •9: Inflammatory Diseases
- •Acute Posterior Multifocal Placoid Pigment Epitheliopathy
- •Acute Retinal Necrosis
- •Cytomegalovirus Retinitis
- •Diffuse Unilateral Subacute Neuroretinitis
- •Endophthalmitis
- •Intermediate Uveitis
- •Multifocal Choroiditis and Panuveitis
- •Multiple Evanescent White Dot Syndrome
- •Neuroretinitis
- •Posterior Scleritis
- •Presumed Ocular Histoplasmosis Syndrome
- •Sarcoidosis
- •Syphilis
- •Systemic Lupus Erythematosus
- •Toxocariasis
- •Toxoplasmosis
- •Tuberculosis
- •Vogt-Koyanagi-Harada Syndrome
- •10: Trauma
- •Choroidal Rupture
- •Commotio Retinae
- •Optic Nerve Avulsion
- •Shaken Baby Syndrome
- •Valsalva Retinopathy
- •11: Peripheral Retinal Diseases
- •Cystic Retinal Tufts
- •Lattice Degeneration
- •Retinal Breaks
- •Retinal Detachment
- •Senile (Adult-Onset) Retinoschisis
- •12: Diseases of the Vitreous
- •Amyloidosis
- •Asteroid Hyalosis
- •Idiopathic Vitritis
- •Persistent Hyperplastic Primary Vitreous
- •Posterior Vitreous Detachment
- •Proliferative Vitreoretinopathy
- •Vitreous Hemorrhage
- •13: Histopathology of Retinal Diseases
- •Macular Diseases
- •Retinal Vascular Diseases
- •Intraocular Tumors
- •Inflammatory Diseases
- •Trauma
- •Peripheral Retinal Diseases
- •14: Clinical Trials in Retina
- •The Diabetic Retinopathy Study
- •The Early Treatment Diabetic Retinopathy Study
- •The Diabetic Retinopathy Vitrectomy Study
- •The Diabetes Control and Complications Trial
- •The Branch Vein Occlusion Study
- •The Central Vein Occlusion Study
- •The Multicenter Trial of Cryotherapy for Retinopathy of Prematurity
- •The Macular Photocoagulation Study
- •The Treatment of Age-Related Macular Degeneration With Photodynamic Therapy (TAP) Study
- •Branch Retinal Vein Occlusion: Macular Edema
- •Branch Retinal Vein Occlusion: Neovascularization
- •Central Serous Chorioretinopathy
- •Central Retinal Vein Occlusion
- •Choroidal Neovascularization
- •Diabetic Retinopathy: Clinically Significant Macular Edema
- •Diabetic Retinopathy: High-Risk Proliferative Diabetic Retinopathy
- •Peripheral Retinal Neovascularization
- •Retinal Arterial Macroaneurysm
- •Retinal Tears and Retinal Detachment
- •Retinal Telangiectasis and Retinal Angiomas
- •Photodynamic Therapy with Verteporfin
- •Index
Return to Quiz
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C H A P T E R 12 Diseases of the Vitreous |
VITREOUS HEMORRHAGE
Vitreous hemorrhage is a significant cause of sudden vision loss. Vitreous hemorrhage can be due to a wide variety of causes including proliferative diabetic retinopathy, posterior vitreous detachment (PVD) with or without retinal tear or retinal detachment, and other retinal vascular, hereditary, and inflammatory diseases.
Symptoms
Most patients experience an acute loss of vision. It is not unusual for the hemorrhage to occur at night and the visual loss is first noticed by the patient on waking. Some patients, particularly patients with diabetes,
report seeing a distinct red stream as the bleeding occurs. Associated symptoms of flashing lights may indicate an underlying PVD or retinal tear.
Clinical Features
On slit lamp examination, red blood cells may be seen on the posterior lens surface and in the anterior vitreous directly behind the lens. Blood may be present in the vitreous cavity (intravitreal hemorrhage) or behind the vitreous (subhyaloid hemorrhage). If the vitreous hemorrhage does not resolve within a few weeks, the blood will lose its hemoglobin and will become gray or white in color. Occasionally, red blood cells migrate into the anterior chamber, and these cells may obstruct the trabecular meshwork, causing a rise in intraocular pressure.
Vitreous hemorrhage is often accompanied by other retinal findings including posterior vitreous detachment, retinal tear or detachment, vein occlusion, proliferative diabetic retinopathy, trauma, macroaneurysm, or macular degeneration.
Ancillary Testing
Ultrasound examination is invaluable in the assessment of eyes with significant vitreous hemorrhage. Detection of a posterior vitreous detachment, submacular hemorrhage, and even large retinal tears is possible with B-scan echography. Serial ultrasound examinations
are required to follow up patients in the absence of an adequate view of the retina.
Pathology/Pathogenesis
A PVD with or without a retinal tear or retinal detachment can cause vitreous hemorrhage by exerting traction on a retinal blood vessel. Abnormal retinal vessels in diabetic retinopathy, retinal vein occlusions, or other proliferative retinopathies can bleed because of vitreous traction on the preretinal blood vessels. Other causes
of vitreous hemorrhage include choroidal neovascularization with “breakthrough bleeding,” X-linked juvenile retinoschisis, and subarachnoid hemorrhage (Terson’s syndrome).
Treatment/Prognosis
Vitreous hemorrhage will generally clear spontaneously, and vision will return as long as the underlying cause is treated. Nonclearing vitreous hemorrhage may be treated with elective pars plana vitrectomy, although urgent intervention is required in the presence of retinal detachment.
System Evaluation
Vitreous hemorrhage is often associated with diabetes and hypertension; these conditions should be tested for in the absence of a definite underlying cause.
C H A P T E R 12 Diseases of the Vitreous |
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Proliferative diabetic retinopathy is a common cause of vitreous hemorrhage. The vitreous provides a scaffold for the proliferation of the new vessels. Contraction of the vitreous may lead to vitreous hemorrhage or traction retinal detachment.
Posterior vitreous detachment (PVD) may be associated with vitreous even in the absence of retinal tear or detachment. This patient with an acute PVD has a vitreous hemorrhage extending from a retinal vessel.
In patients with regressed neovascularization following laser photocoagulation, posterior vitreous detachment may lead to vitreous hemorrhage.
The presence of a vitreous hemorrhage in the setting of acute posterior vitreous detachment raises the suspicion of a retinal tear or detachment.
Breakthrough vitreous bleeding may occur in patients with exudative age-related macular degeneration and massive subretinal hemorrhage.
Fundus photograph of a patient with chronic vitreous hemorrhage related to proliferative diabetic retinopathy. Note the yellow coloration of the vitreous hemorrhage due to changed hemoglobin.
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C H A P T E R 12 Diseases of the Vitreous |
SELECTED REFERENCES
Amyloidosis
1.Doft BH, Machemer R, Skinner M, et al. Pars plana vitrectomy for vitreous amyloidosis. Ophthalmology. 1987;94:607–611.
2.Gorevic PD, Rodrigues MM. Ocular amyloidosis. Am J Ophthalmol. 1994;117:529–532.
Asteroid Hyalosis
1.Moss SE, Klein R, Klein BE. Asteroid hyalosis in a population: the Beaver Dam eye study. Am J Ophthalmol. 2001;132:70–75.
2.Parnes RE, Zakov ZN, Novak MA, Rice TA. Vitrectomy in patients with decreased visual acuity secondary to asteroid hyalosis. Am J Ophthalmol. 1998;125:703–704.
3.Winkler J, Lunsdorf H. Ultrastructure and composition of asteroid bodies. Invest Ophthalmol Vis Sci.
2001;42:902–907.
Idiopathic Vitritis
1.Brinton GS, Osher RH, Gass JDM. Idiopathic vitritis. Retina. 1983;3:95–98.
2.Gass JDM. Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment. 4th ed. St. Louis: Mosby, Inc; 1997:708–709.
3.Johnson LA, Wirostko E. Chronic idiopathic vitritis: ultrastructural properties of bacteria-like bodies within vitreous leukocyte phagolysosomes. Am J Clin Pathol. 1986;86:19–24.
Persistent Hyperplastic Primary Vitreous
1.Dass AB, Trese MT. Surgical results of persistent hyperplastic primary vitreous. Ophthalmology. 1999;106:280–284.
2.Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture. Am J Ophthalmol. 1997;124:587–626.
3.Reese AB. Persistent hyperplastic primary vitreous. Am J Ophthalmol. 1955;40:317–331.
Posterior Vitreous Detachment
1.Byer NE. Natural history of posterior vitreous detachment with early management as the premier line of defense against retinal detachment. Ophthalmology. 1994;101:1503–1513.
2.Novak MA, Welch RB. Complications of acute symptomatic posterior vitreous detachment. Am J Ophthalmol. 1984;97:308–314.
3.Preferred Practice Pattern. Management of posterior vitreous detachment, retinal breaks, and lattice degeneration. #110022 American Academy of Ophthalmology; 1998.
4.Tanner V, Harle D, Tan J, et al. Acute posterior vitreous detachment: the predictive value of vitreous pigment and symptomatology. Br J Ophthalmol. 2000;84:1264–1268.
Proliferative Vitreoretinopathy
1.Asaria RH, Kon CH, Bunce C, et al. How to predict proliferative vitreoretinopathy: a prospective study. Ophthalmology. 2001;108:1184–1186.
2.Charteris CG. Proliferative vitreoretinopathy: pathobiology, surgical management and adjunctive treatment. Br J Ophthalmol. 1995;79:953–960.
3.Machemer R, Aaberg TM, Freeman HM, et al. An updated classification of retinal detachment with proliferative vitreoretinopathy. Am J Ophthalmol. 1991;112:159–165.
Vitreous Hemorrhage
1.DeBernardo C, Blodi B, Byrne SF. Echographic evaluation of retinal tears in patients with spontaneous vitreous hemorrhage. Arch Ophthalmol. 1992;110:511–514.
2.Sarrafizadeh R, Hassan TS, Ruby TS, et al. Incidence of retinal detachment and visual outcome in eyes presenting with posterior vitreous separation and dense fundusobscuring vitreous hemorrhage. Ophthalmology. 2001;108:2273–2278.
