Abnormal Ocular Findings
Am Fam Physician. 2003 Sep 1;68(5):933-934.
A 78-year-old woman with type 2 diabetes of 15 years' duration presented for a regular checkup. Abnormal ocular fundus findings were seen bilaterally, as shown in Figure 1. She complained of mild blurred vision (visual acuity was 20/40 in both eyes), and she mentioned that she had previously been diagnosed with “early cataracts.” She further stated she had been using “very thick glasses”since childhood and that her vision had always been below normal.
Based on the patient's history and physical examination, which one of the following is the most probable diagnosis?
A. Idiopathic macular hole
B. Fundus of high myopia
C. Diabetic retinopathy
D. Retinitis pigmentosa
E. Cytomegalovirus chorioretinitis
The answer is B: fundus of high myopia. These fundal changes usually are seen in patients with more than–6.00 diopters of myopia, although in rare cases, they can be found in persons with milder refractive errors.1–3 Fundal changes from high myopia include a broad spectrum of abnormalities. Peripapillary chorioretinal atrophy is the most common finding and is seen as a white rim of visible sclera around the optic disc (area between the dotted lines in Figure 2). Areas of atrophic retinal pigment epithelium also may be found in the macular area (Figure 1).
Myopic fundal changes may include more serious findings. “Lacquer cracks” are yellow-white lines representing choroidal cracks, secondary to the mechanical stretching that occurs with the increased length of the eyeball in myopia. Macular hemorrhages and choroidal neovascularization can lead to a drastic decrease in visual acuity. Fuchs' spot describes a round or elliptic elevated dark brown lesion located in the macula that arises because of choroidal neovascularization (Figure 3). In the myopic patient, it is important to examine the periphery of the retina because of an increased risk of retinal tears, which can predispose to retinal detachment.
While myopia is a highly common condition, high myopia affects about 2 percent of the population.3 Choroidal neovascularization is seen in 5 to 10 percent of high myopic eyes. High myopia is the most common cause of choroidal neovascular changes in the younger population, while macular degeneration accounts for most cases in older age groups.4
Idiopathic macular holes would present with smaller, more discrete lesions than the large pallorous areas seen in this patient. The choroid remains unaffected in this condition.
Early nonproliferative diabetic retinopathy findings include dot hemorrhages and exudates, but would not cause large, confluent areas of retinal whitening.
Retinitis pigmentosa, a hereditary condition, shows a characteristic “bone spicule” peripheral pigmentation that usually spares the macula until more advanced stages.
Cytomegalovirus chorioretinitis classically presents with the “scrambled eggs and ketchup” fundal appearance of scattered exudates and hemorrhages. Confluent areas of pallor without any bleeding would not be typical.
1. Flynn, HW. Acquired diseases affecting the macula. In: Retina and vitreous, 2002–2003. San Francisco, Calif.: American Academy of Ophthalmology, 2002.
2. Vander JF, Ducker JS, Jaeger EA. Miscellaneous diseases of the fundus. In: Duane's Clinical ophthalmology on CD-ROM. Philadelphia: Lippincott Williams & Wilkins, 2002.
3. Tabandeh H, Flynn HW Jr, Scott IU, Lewis ML, Rosenfeld PJ, Rodriguez F, et al. Visual acuity outcomes of patients 50 years of age and older with high myopia and untreated choroidal neovascularization. Ophthalmology. 1999;106:2063–7.
4. Cohen SY, Laroche A, Leguen Y, Soubrane G, Coscas GJ. Etiology of choroidal neovascularization in young patients. Ophthalmology. 1996;103:1241–4.
The editors of AFP welcome submissions for Photo Quiz. Guidelines for preparing and submitting a Photo Quiz manuscript can be found in the Authors' Guide at http://www.aafp.org/afp/photoquizinfo. To be considered for publication, submissions must meet these guidelines. E-mail submissions to firstname.lastname@example.org.
Copyright © 2003 by the American Academy of Family Physicians.
This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. Contact email@example.com for copyright questions and/or permission requests.
Want to use this article elsewhere? Get Permissions