Clinicopathologic Reports, Case Reports, and Small Case Series
May 2006

Optical Coherence Tomography Demonstration of Macular Infarction in Sickle Cell Retinopathy

Author Affiliations



Copyright 2006 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.2006

Arch Ophthalmol. 2006;124(5):746-747. doi:10.1001/archopht.124.5.746

Sickle cell retinopathy is caused by retinal ischemia secondary to the sickling of red blood cells in retinal arterioles, which supply nutrients to the ganglion cell layer, inner nuclear layer, and Muellerian glia of the retina. Macular infarction due to sickle cell disease has been documented using fluorescein angiography, electroretinography, and histopathologic examination.13 However, optical coherence tomography (OCT) of sickle cell retinopathy has, to our knowledge, never previously been reported. We report a case of macular atrophy secondary to retinal arteriolar occlusion in a patient with sickle cell disease, documented by standard-resolution OCT and ultra-high-resolution OCT, a new imaging technology capable of 2- to 3-μm resolution in the axial direction4 compared with 10 μm with standard-resolution OCT.5

Report of a Case

A 26-year-old man with sickle cell disease (HbSS) went to the emergency department during an acute sickle cell crisis and was admitted to the medical intensive care unit with myocardial infarction, acute renal failure, and cholecystitis. He was referred to the retina service at the New England Eye Center, Boston, Mass, with a sudden decrease in visual acuity in both eyes and with central distortion in the left eye. On examination, uncorrected visual acuity measured 20/60 OD and counting fingers OS, without improvement on manifest refraction in the left eye. Intraocular pressures were 10 mm Hg OD and 12 mm Hg OS. Anterior segment examination was unremarkable in both eyes. Retinal whitening secondary to occlusion of branch arterioles was present in both eyes, with involvement of the fovea in the left eye (Figure 1A and B). Peripheral retinal examination demonstrated involuted neovascular fronds with evidence of peripheral nonperfusion in both eyes. Visual acuity remained stable 1 month following the patient's visit, with resolution of the retinal whitening. Residual, fine retinal pigment epithelium changes in the area of arteriolar occlusion were visible (not shown).

Figure 1
Image not available

Fundus photograph of the right eye at the initial visit, showing retinal whitening in the distribution of the retinal arteriolar occlusions in the macula (A), and fundus photograph of the left eye at the initial visit, showing retinal whitening in the distribution of the retinal arteriolar occlusions in the macula, including the fovea (B).

Standard-resolution OCT images obtained at the 1-month follow-up visit demonstrated marked thinning of the retina in the temporal macula of both eyes, with greater foveal involvement in the left eye (Figure 2A and B). Ultra-high resolution OCT was performed, which again showed thinning of the temporal macula in both eyes, specifically involving inner retinal layers while sparing the photoreceptor and retinal pigment epithelium layers (Figure 2C).

Figure 2
Image not available

All of the optical coherence tomographic images were taken from the left eye 5 weeks after the initial visit. A, Macular map (6-mm-diameter) digitally created from 6 standard-resolution optical coherence tomographic images. Note the marked thinning of the temporal macula, including the fovea, corresponding to the whitened area in Figure 1B. B, Horizontal 6-mm standard-resolution macular image. C, Horizontal 6-mm ultra-high resolution optical coherence tomographic macular image. Nasally, the retina appears normal with all of the retinal layers intact. Temporally, the inner retinal layers are atrophic whereas the outer nuclear layer remains a normal thickness (see measurements). NFL indicates nerve fiber layer; GCL, ganglion cell layer; IPL, inner plexiform layer; INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer; ELM, external limiting membrane; IS/OS, junction between inner and outer photoreceptor segments; and RPE, retinal pigment epithelium.


The retinal vessels supply blood to the ganglion cell and inner nuclear layers of the retina whereas the choriocapillaris nourishes the photoreceptors and the retinal pigment epithelium.6 As vessels in the choriocapillaris are of larger caliber, it is rare for them to occlude and cause outer retinal ischemia. However, the inner retinal layers are prone to ischemia, as the retinal vessels are end arterioles and capillaries. Histopathologic studies3,7 of sickle cell retinopathy and other vaso-occlusive diseases have previously shown selective atrophy of the inner retinal layers of the macula in several eyes after retinal infarction.

Our patient had clinically visible whitening in circumscribed areas of the macula on his initial visit. Five weeks later, macular thinning was noted in these ischemic areas on standard-resolution OCT, contrasting with regions of normal retinal thickness where vessels were left unoccluded. Ultra-high resolution OCT showed the retinal atrophy to specifically involve the inner retinal layers while sparing the photoreceptors and the retinal pigment epithelium. We would expect to see similar findings in other arteriolar occlusive diseases of the retina. The measurement of retinal thinning with OCT might therefore be useful to document retinal infarction and its repair in patients with known vaso-occlusive disease.

Back to top
Article Information

Correspondence: Dr Rogers, Department of Ophthalmology, Tufts–New England Medical Center, 750 Washington St, Box 450, Boston, MA 02111 (

Author Contributions: Dr Rogers had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Financial Disclosure: Drs Fujimoto and Schuman receive royalties from intellectual property licensed by Massachusetts Institute of Technology, Cambridge, to Carl Zeiss Meditec, Dublin, Calif, and they receive research support from Carl Zeiss Meditec.

Funding/Support: This work was supported in part by grants RO1-EY11289-16, R01-EY13178, and P30-EY13078 from the National Institutes of Health, Bethesda, Md, ECS-0119452 from the National Science Foundation, Arlington, Va, F49620-98-1-0139 from the Air Force Office of Scientific Research, Arlington, and F49620-01-1-0186 from the Medical Free Electron Laser Program, Washington, DC, and by Carl Zeiss Meditec.

Knapp  JW Isolated macular infarction in sickle cell (SS) disease. Am J Ophthalmol 1972;73857- 859
Acacio  IGoldberg  MF Peripapillary and macular vessel occlusions in sickle cell anemia. Am J Ophthalmol 1973;75861- 866
Romayanada  NGoldberg  MFGreen  WR Histopathology of sickle cell retinopathy. Trans Am Acad Ophthalmol Otolaryngol 1973;77OP642- OP676
Drexler  WMorgner  UGhanta  RKKärtner  FXSchuman  JSFujimoto  JG Ultrahigh-resolution ophthalmic optical coherence tomography. Nat Med 2001;7502- 507
Huang  DSwanson  EALin  CP  et al.  Optical coherence tomography. Science 1991;2541178- 1181
Gass  JDM Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment. 4th St Louis, Mo Mosby–Year Book Inc1997;12
Foos  RY Regional ischemic infarcts of the retina. Albrecht Von Graefes Arch Klin Exp Ophthalmol 1976;200183- 194