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Computed Tomographic Diagnosis of Posterior Ocular Staphyloma · 90 Computed Tomographic Diagnosis...

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90 Computed Tomographic Diagnosis of Posterior Ocular Staphyloma Robert L. Anderson ,' Gil A. Epstein ,2 and Edward A. Dauer" 3 With cons tantly improving tec hnology and more frequent comp uted tomogr ap hy (CT) of the brain and orbits, the radiologist is likely to e ncount er various ophthalmologic co nditions with which he is unfamiliar. One such condition, which has not been described previously, is the posterior oc ular staphyloma. The following case presentation will serve to illustrate the clinical and CT manifestations of this condition. Case Report A 66-year-old woman was seen by a neurologist with a 2 year history of inter mittent headac hes ref er red to the right eye and face. She reported a long history of poor vision in the right eye. Physical and neurologic examinati on revealed only severe myopia in the ri ght eye. CT of th e br ain and orbits was performed with a Pi cke r Synerview 600 CT Scanner, 256 x 256 mat ri x, 3.3 sec scan time, 10 mm sec ti ons angled 20 ° above the canthomeatal line anteriorly for brain, 6 mm sect ions parallel to infraorbital-meatal line for orbits. Images were obtained before and after bolus infusion of 100 ml Con ray 60 (methylglucamine iot halamate 60%, Mallin ck rodt). The orbital examination (fig. 1) revealed a superolateral isodense bulge projecting from th e posterior aspec t of the right globe with apparent thinning or absence of the scleral-uveal rim on the con- trast-enhanced images. There was no appreciable enhancement of the mass (bul ge). The optic ner ve and ex tr aocular mu sc les were sy mmetric and of normal th ick ness. There was no evidence of proptosi s. Th e ce rebral sca n was normal. The oc ular examinati on revealed severe myopia best co rr ec ted to finger counting on the right, with 20/ 20 vision on the left. A Marcus-Gunn afferent pupillary defect was present on the right. Fundu scopy revealed a myopic fundus with a lar ge posterior sta- phyloma. The axial length of each eye was deter mined by sonog- raphy, the right measuring 30.66 mm , the left 24.1 mm , co nfirming the fundus co pic findings. The sag ittal sonogram correlated well with sagittal CT reconstruction (fig. 2). Discussion The posterior staphyloma is a we ll recog nized entity as- soc iated with the highly myopic eye. High myopia may Received January 14 , 1 982; accepted after revision April 27, 1 982. involve one or both eyes and is often hereditary . The highly myopic eye is characteristically egg-shaped, as compared with the more spherical " normal" eye. The elongation is in the anteroposterior axis, affecting the posterior pole. The anterior half of the eye is normal [1 -3]. There is usually no proptosis. The elongation is thought to be due to a defective sclera, the collagenous structural outercoat of the eye. When severe, there is a focal outward bulge of the sclera at the posterior pole, a posterior staphyloma [2]. Adjacent layers of the eye, the retina, and choroid are likewise thinned and bulge outward with the sclera . This results in a retina prone to detachment [3]. Visual prognosis is poor, especially with congenital and asymmetric staphyloma . In most cases, there is no effective treatment. Scleral implants have met with limited success [1 , 3]. Other co nditions in which staphyloma oc c ur include glau- co ma, scleritis, trauma, and necrotizing infections . These co nditions are easily distinguished clinically [3]. The poste- rior staphyloma and the myopic fundus are diagnosed by clini ca l ophthalmoscopy and ca n be quantified by sonogra- phy. The CT appearances correlate well with the structural changes . The scleral-uveal rim was noted to be thinned or absent at the site of the posterior ocular bulge. The bulge was isodense with the rest of the vitreous. The lack of enhancement following contrast is to be ex pected. This CT pattern is unlikely to be encountered in ocular neoplasm (primary or metastatic) or pseudotumor . In the Bernardino et al. [4] series of ocular neoplasms , " all showed ecce ntric thickening of the scleral-uveal rim with extension into the globe ." Pseudotumors likewise frequently show scleral-uveal rim thickening and marked enhancement [4- 8]. In neither condition is one likely to encounter a smooth focal bulge projecting from the globe of density identical to the vitreous before and after contrast administration. While Hilal and Trokel [5] noted that CT would demon- strate num ero us conditions such as congenital glaucoma (m anifest by a large globe), they indic ated these conditions are more easily assessed by conventional optical and son- ographic methods. Although this is true, an awareness of 'Department of Radiology, Fl orida Medica l Center, 5000 W. Oak land Park, Fort Lauderdale, FL 33313. Addr ess reprint requests to E. A. Dauer. ' Department of Ophthalmology, Florida Medica l Center, Fort Lauderdale, FL 333 1 3. 3Department of Radiol ogy , University of Miami, Miami, FL 33 1 52. AJNR 4:90-91, January / February 1983 0195-6 1 08 / 83 / 040 1-0090 $00.00 © Ameri ca n Roent gen Ray Society
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Page 1: Computed Tomographic Diagnosis of Posterior Ocular Staphyloma · 90 Computed Tomographic Diagnosis of Posterior Ocular Staphyloma Robert L. Anderson,' Gil A. Epstein,2 and Edward

90

Computed Tomographic Diagnosis of Posterior Ocular Staphyloma Robert L. Anderson ,' Gil A. Epstein ,2 and Edward A. Dauer" 3

With constantly improving technology and more frequent computed tomography (CT) of the brain and orbits, the rad iologist is likely to encounter various ophthalmologic conditions with which he is unfamiliar . One such condition, which has not been desc ribed previously, is the posterior ocular staphyloma. The following case presentation will serve to illustrate the c linical and CT manifestations of this condition.

Case Report

A 66-year-old woman was seen by a neurolog ist with a 2 year history of intermittent headaches referred to the right eye and face. She reported a long history of poor vision in the right eye . Physical and neurologic examination revealed only severe myopia in the right eye.

CT of the brain and orbits was performed with a Picker Synerview 600 CT Scanner, 256 x 256 matri x, 3.3 sec scan time, 10 mm sections angled 20° above the canthomeatal line anteriorly for brain , 6 mm sect ions parallel to infraorbital-meatal line for orbits. Images were obtained before and after bolus infusion of 100 ml Con ray 60 (methylglucamine iothalamate 60%, Mallinck rodt) .

The orbital examinat ion (fig . 1) revealed a superolateral isodense bulge projecting from th e posterior aspect of the right globe with apparent thinning or absence of the scleral-uveal rim on the con­trast-enhanced images. There was no appreciable enhancement of the mass (bulge). The optic nerve and extraocular muscles were symmetric and of normal th ickness. There was no evidence of proptosis. The cerebral scan was normal.

The ocular examination revealed severe myopia best corrected to finger cou nting on the right , with 20 / 20 vision on the left. A Marcus-Gunn afferent pupillary defect was present on the right. Funduscopy revealed a myopic fundus with a large posterior sta­phyloma. The axial length of each eye was determined by sonog­raphy , the right measuring 30.66 mm , the left 24.1 mm , confirming the funduscopic findings. The sagittal sonogram correlated well with sag ittal CT recon struc tion (fig. 2).

Discussion

The posterior staphyloma is a well recognized entity as­soc iated with the highly myopic eye. High myopia may

Received January 14, 1982; accepted after revision Apri l 27, 1982.

involve one or both eyes and is often hereditary. The highly myopic eye is characteristically egg-shaped, as compared with the more spherical " normal " eye. The elongation is in the anteroposterior axis, affecting the posterior pole. The anterior half of the eye is normal [1 -3]. There is usually no proptosis . The elongation is thought to be due to a defective sclera, the collagenous structural outercoat of the eye. When severe, there is a focal outward bulge of the sclera at the posterior pole , a posterior staphyloma [2]. Adjacent layers of the eye, the retina, and choroid are likewise thinned and bulge outward with the sclera. This results in a retina prone to detachment [3]. Visual prognosis is poor, especially with congenital and asymmetric staphyloma. In most cases, there is no effective treatment. Scleral implants have met with limited success [1 , 3].

Other conditions in which staphyloma occur include glau­coma, scleritis, trauma, and necrotizing infections . These conditions are easily distinguished clinically [3]. The poste­rior staphyloma and the myopic fundus are diagnosed by c linical ophthalmoscopy and can be quantified by sonogra­phy.

The CT appearances correlate well with the structural changes. The scleral-uveal rim was noted to be thinned or absent at the site of the posterior ocular bulge. The bulge was isodense with the rest of the vitreous. The lack of enhancement following contrast is to be expected.

This CT pattern is unlikely to be encountered in ocular neoplasm (primary or metastatic) or pseudotumor. In the Bernardino et al. [4] series of ocular neoplasms, " all showed eccentric thickening of the scleral-uveal rim with extension into the globe." Pseudotumors likewise frequently show scleral-uveal rim thickening and marked enhancement [4-8]. In neither condition is one likely to encounter a smooth focal bulge projecting from the globe of density identical to the vitreous before and after contrast administration.

While Hilal and Trokel [5] noted that CT would demon­strate numerous conditions such as congenital glaucoma (manifest by a large globe), they indicated these conditions are more easily assessed by conventional optical and son­ographic methods. Although this is true , an awareness of

' Departmen t of Radiology, Florida Medical Center, 5000 W. Oakland Park , Fort Lauderdale, FL 33313. Address reprint requests to E. A. Dauer. ' Department of Ophthalmology, Florida Medical Center, Fort Lauderdale, FL 33313. 3Department of Radiology, University of Miami , Miami, FL 33152.

AJNR 4:90-91, January / February 1983 0195-6108 / 83 / 0401-0090 $00.00 © American Roentgen Ray Society

Page 2: Computed Tomographic Diagnosis of Posterior Ocular Staphyloma · 90 Computed Tomographic Diagnosis of Posterior Ocular Staphyloma Robert L. Anderson,' Gil A. Epstein,2 and Edward

AJNR:4, Jan ./ Feb. 1983 CT OF POSTERIOR STAPHYLOMA 91

Fig . 1.- Nonenhanced (A) and en­hanced (B) CT scans. Posterior staphy­loma is isodense focal bu lge of supero­lateral aspect of posterior po le of right globe. Thinning or absence of overlying sc leral-uveal rim (arrows).

A

B

A

Fig . 2.-A, Sagittal sonogram. Posterior staphyloma (arrows) . B, Corre­spond ing CT reconstruction.

B

these condit ions and their CT appearance will help the rad iolog ist avoid undue concern caused by the erroneous d iagnosis of an ocu lar / orbital mass . We suggest that the CT pattern described in our case is characteristic enough to permit the radiologist to at least include posterior staphy­loma in his differential d iagnosis. The condition is then readily confirmed by funduscopic and / or sonographic ex­amination.

REFERENCES

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Vaugh D, Asbury T. General opthalmology. Los Altos, CA: Lange, 1974:85-89 Duke-Elder S. Parsons diseases of the eye. London: Churchi ll , 1956 :442-443 Duke-Elder S, Abrams O. Systems of ophthalmology. Vol V: Opthalmic optics and refraction. St. Lou is: Mosby, 1970: 307-309 Bernardino ME, Danziger J, Young SE, Wallace S. Computed tomography in ocular neoplastic disease. AJR 1978;131 : 111-11 3 Hilal SK, Trokel SL. Computerized tomography of the orbit using thin sect ions. Semin Roentgenol 1977; 12: 137 -14 7 Hilal SK. Computed tomography of the orbit. Ophthalmology (Rochester) 1979;86: 864-870 Bernardino ME, Zimmerman RD, Cirtin CM , Davis DO. Scleral th ickening: a CT sign of orbital pseudotumor. AJR 1977;129 :703-706 Guibert-Trani er F, Piton J, Culabet A, Caille JM. Orbital Syn­dromes- CT analysis of 100 cases. Comput Tomogr 1979;3: 241 -264


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