- •Preface
- •Basic physics
- •Acoustic Wave
- •Laws of Acoustic Energy
- •Frequency and Resolution
- •Instrumentation
- •A-scan
- •Biometric A-scan
- •Standardized A-scan
- •B-scan
- •Special techniques
- •Ultrasound Biomicroscopy
- •Immersion B-scan
- •Color Doppler Ultrasonography
- •Three-Dimensional Ultrasonography
- •References
- •Resolution
- •Transducers
- •Clinical use of ultrasound biomicroscopy
- •Technique
- •Measuring Ocular Structures
- •Normal Ocular Structures
- •Anterior chamber
- •The cornea
- •Anterior chamber angle region
- •The iris
- •The ciliary body
- •The zonule
- •Glaucoma
- •Corneal and Scleral Disease
- •Intraocular Lens Complications
- •Trauma
- •Conjunctival and Adnexal Disease
- •Anterior Segment Tumors
- •Iris tumors
- •Ciliary body tumors
- •Extrascleral extension of intraocular tumors
- •Corneal involvement
- •Cysts
- •Peripheral choroidal tumors
- •Future directions
- •References
- •Ophthalmic Biometry
- •Axial eye length measurements
- •Instruments and Methods
- •A-scan Biometry
- •Contact method
- •Immersion technique
- •Velocity Settings
- •Special Clinical Situations
- •Silicone oil
- •Posterior staphyloma
- •Pseudophakic eyes
- •Intraocular lens power calculations
- •Formulas
- •First generation
- •Second generation
- •Third generation
- •Fourth generation
- •Selection of the Best Formula
- •Special Clinical Situations
- •Post refractive surgery
- •Clinical history method
- •Contact lens method
- •K value obtained by topography
- •Double K formulas
- •Post radial keratotomy and cataract surgery
- •References
- •Evaluation of the cornea
- •Congenital Corneal Opacification
- •Corneal Lesions
- •Corneal Dystrophies
- •Refractive Surgery
- •Evaluation of intraocular lenses
- •Posterior Chamber Intraocular Lenses
- •Anterior Chamber Intraocular Lenses
- •Phakic Intraocular Lenses
- •Evaluation of anterior segment trauma
- •Iridocorneal Angle Trauma
- •Foreign Body
- •Surgical Planning
- •Descemet’s Membrane Detachment
- •Summary
- •References
- •Glaucoma
- •Anterior angle evaluation
- •Plateau Iris Configuration
- •Ciliary Body Cysts
- •Pigmentary Glaucoma
- •Synechiae
- •Iridocorneal Endothelial Syndromes
- •Scleritis
- •Evaluation after glaucoma surgery
- •Filtering Bleb
- •Hypotony
- •Choroidal Effusion/Hemorrhage
- •Vitreous Hemorrhage
- •Aqueous Misdirection
- •Glaucoma Drainage Device
- •Congenital glaucoma
- •The future
- •References
- •Vitreoretinal Disorders
- •Vitreous hemorrhage
- •Posterior vitreous detachment
- •Retinal detachment
- •Rhegmatogenous Retinal Detachment
- •Tractional Retinal Detachment
- •Exudative Retinal Detachment
- •Total Retinal Detachment
- •Differential Diagnosis
- •Associated Retinal Detachment
- •Giant Retinal Tear
- •Differential Diagnosis
- •Retinal pigment epithelium detachment
- •Retinoschisis
- •Disciform lesions
- •Postsurgical changes
- •Scleral Buckle
- •MIRAgel Implant
- •Gas/Air Bubbles
- •Silicone oil
- •Retained Perfluorocarbon Liquids
- •References
- •Intraocular Tumors
- •Retinoblastoma
- •Differential diagnosis of retinoblastoma
- •Persistent Hyperplastic Primary Vitreous
- •Coats’ Disease
- •Toxocariasis
- •Medulloepithelioma
- •Benign uveal tumors
- •Iris and Ciliary Body Nevus
- •Choroidal Nevus
- •Uveal Melanocytoma
- •Malignant uveal tumors
- •Iris and Ciliary Body Melanoma
- •Choroidal Melanoma
- •A-scan
- •B-scan
- •Tumor biometry
- •Intraoperative confirmation of plaque placement
- •Response to radiation therapy
- •Differential Diagnosis of Choroidal Melanoma
- •Circumscribed choroidal hemangioma
- •Choroidal metastasis
- •Leiomyoma
- •Age-related macular and extramacular degeneration
- •Posterior scleritis
- •Intraocular calcification
- •Astrocytic Hamartoma
- •Choroidal Osteoma
- •Sclerochoroidal Calcification
- •Others
- •References
- •Uveitis
- •Anterior Uveitis
- •Intermediate Uveitis
- •Pars Planitis
- •Hypotony and Uveitis
- •Posterior Uveitis
- •Panuveitis
- •Sympathetic ophthalmia and Vogt-Koyanagi-Harada syndrome
- •Scleral inflammatory disease
- •Episcleritis
- •Scleritis
- •Anterior scleritis
- •Posterior scleritis
- •Inflammatory leukocoria (toxocariasis)
- •Infectious endophthalmitis
- •Inflammatory orbital diseases
- •References
- •Optic Nerve Disorders
- •Technique
- •30deg Test
- •Papilledema
- •Adults
- •Intracranial pathology
- •Children
- •Optic disc drusen
- •Adults
- •Young Adults
- •Congenital disc anomalies
- •Optic Disc Coloboma
- •Morning Glory Disc Anomaly
- •Tilted Optic Disc
- •Pseudodoubling of the Optic Disc
- •Retrobulbar optic nerve lesions
- •Gaze-evoked amaurosis
- •Giant cell arteritis
- •References
- •Rhegmatogenous retinal detachment
- •Hemorrhagic choroidal detachment
- •Lens dislocation
- •Intraocular foreign body
- •Endophthalmitis
- •References
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Fig.7. (A) Clinical appearance of a pigmented lesion of the iris. (B) Ultrasound biomicroscopy shows a localized iris nevus (T). (From Pavlin CJ, Foster FS. Ultrasound biomicroscopy of the eye. New York: Springer Verlag; 1994. p. 101; with kind permission of Springer Science and Business Media.)
When observation is elected, lesions may be followed with greater precision. Where surgical intervention is indicated, the information gained is helpful in planning the approach.
Iris tumors
The presence of a typical morphologic appearance on ultrasound biomicroscopy may be helpful as a diagnostic sign. Several small, minimally elevated lesions involving the peripheral iris and clinically considered nevi have a similar appearance on ultrasound biomicroscopy (Fig. 7). They share the ultrasound biomicroscopic appearance of a small moderately thickened iris lesion not extending past the iris root. There is frequently a hypoechoic layer on the surface of these lesions, possibly indicating that the superficial layer is involved with the closely spaced cells of a surface plaque.
It is difficult to be too specific as to histologic diagnosis with ultrasound, even with the added
detail presented by ultrasound biomicroscopy. Resolution is not at the level that can differentiate individual cells. Malignant melanomas of the iris can be variable in their clinical and ultrasonic presentation. Ultrasound biomicroscopy can be helpful in a number of ways. Internal reflectivity varies considerably depending on the degree of vascularity and the patterns of internal cellular structure. Some melanomas show a linear internal pattern, others show a uniform reflectivity, while others show a large degree of internal vascularity.
Ciliary body tumors
One of the major assets of ultrasound biomicroscopy is the ability to differentiate a peripheral localized iris lesion from a ciliary body tumor that involves the iris (Fig. 8). These lesions can look very similar clinically as can be appreciated in Figs. 7A and 8A.
Ciliary body tumors can be easily assessed, although large tumors (>4 mm in depth) cannot be
Fig. 8. (A) Clinical appearance of a pigmented iris tumor. (B) Ultrasound biomicroscopy shows a ciliary body melanoma (T) with iris involvement. (From Pavlin CJ, Foster FS. Ultrasound biomicroscopy of the eye. New York: Springer Verlag; 1994. p. 101; with kind permission of Springer Science and Business Media.)
Ultrasound Biomicroscopy |
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Fig. 9. (A) Pigmented lesion on the sclera. (B) Ultrasound biomicroscopy shows that this is extrascleral extension (arrow) of choroidal tumor (T). (From Pavlin CJ, Foster FS. Ultrasound biomicroscopy of the eye. New York: Springer Verlag; 1994. p. 135; with kind permission of Springer Science and Business Media.)
Fig.10. (A) Clinical appearance of a tumor involving the cornea. (B) Ultrasound biomicroscopy shows that the tumor (T) is superficial and that Bowman’s membrane is intact over the cornea (C). (From Pavlin CJ, Foster FS. High Resolution Ultrasound. In: Krachmer JH, Mannis MJ, Holland EJ, editors. The Cornea. Mosby-Year book Inc.: St. Louis; 2004; with permission.)
Fig.11. (A) Clinical appearance of a tumor involving the cornea. (B) Ultrasound biomicroscopy shows deep involvement of all corneal layers (T). (From Pavlin CJ, Foster FS. High Resolution Ultrasound. In: Krachmer JH, Mannis MJ, Holland EJ, editors. The Cornea. Mosby-Year book Inc.: St. Louis; 2004; with permission.)
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Fig. 12. Iridociliary cyst (arrow) under the iris.
completely imaged because of sound attenuation. Small lesions that cannot be detected by conventional ultrasound can be defined by ultrasound biomicroscopy. Larger ciliary body lesions are detectable by conventional ultrasound, but ultrasound biomicroscopy shows improved internal detail of the superficial part of the tumor and frequently allows a more precise localization of the posterior and lateral boundaries. This information is important if iridocyclectomy is considered as a possible treatment.
The lateral extension of the tumor can be clearly defined, which can be important in the diagnosis of ring melanoma. These patients frequently present with hyperchromic glaucoma with delayed diagnosis. Ultrasound biomicroscopy is the best method of making the diagnosis in these cases.
Extrascleral extension of intraocular tumors
In cases of extrascleral extension, the relationship of the tumor to the extrascleral component can be defined (Fig. 9). The extrascleral component generally is located just above the internal ocular
tumor. Both of the lesions can be imaged simultaneously with ultrasound biomicroscopy. Frequently, the transscleral connection is imaged.37
Corneal involvement
Tumors that involve the cornea can present difficulty in determining the depth of corneal involvement. Ultrasound biomicroscopy can generally determine the thickness of the tumor and which corneal layers are involved (Figs. 10 and 11).38 This information can have a direct bearing on the type of treatment required. Tumors that are above Bowman’s membrane can generally be surgically removed, leaving the cornea intact. Deeper involvement may require a radiotherapeutic approach to preserve the cornea.
Cysts
Cysts are clearly imaged by ultrasound biomicroscopy.39,40 The usual clinical presentation of an iridociliary cyst is an elevation of the peripheral iris without iris involvement. The typical ultrasound biomicroscopic appearance of a thin-walled cyst with no internal reflectivity is diagnostic and essentially eliminates any question as to whether a lesion is a cyst or solid tumor (Fig. 12). If the iris is not involved, a cyst would be the most common clinical diagnoses. Occasionally, a ciliary body tumor with an extension under the iris can have this same presentation. Small cysts are also found occasionally as an isolated finding on examination for some other clinical indication or in association with solid lesions of the iris or ciliary body.
Peripheral choroidal tumors
The anterior aspect of peripherally located choroidal tumors can be imaged by ultrasound biomicroscopy.41 Although it is often impossible to measure these tumors through their greatest thickness, valuable information can be gained
Fig.13. (A) Histology of a choroidal tumor (T) stripping the ciliary body (cb) from the sclera (S), producing a small fluid space (arrow). (B) Ultrasound biomicroscopy image of same tumor showing these features.
