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Published on: July 6, 2013
[Cytomegalovirus retinitis in immunocompetent patients]
Wakako Yoshinaga1, Yuka Mizushima, Noriko Abematsu
1Department of Ophthalmology Kagoshima University Graduate School of Medical and Dental Sciences, Japan. wakako-y@m2.kufm.kagoshima-u.ac.jp
Insights
Cytomegalovirus (CMV) retinitis is rare in immunocompetent individuals. Two diabetic patients experienced indolent CMV retinitis that resolved without antiviral treatment, suggesting a potential link.
Area of Science:
- Ophthalmology
- Infectious Diseases
- Virology
Background:
- Cytomegalovirus (CMV) retinitis typically affects severely immunocompromised patients.
- This report details two cases of CMV retinitis in immunocompetent individuals.
Observation:
- Two immunocompetent male patients, aged 65 and 63, presented with blurred vision and floaters.
- Ophthalmologic examinations revealed anterior chamber inflammation, vitreous opacity, and peripheral retinal lesions.
- CMV DNA was detected in aqueous humor, confirming CMV retinitis.
Findings:
- Both cases exhibited indolent CMV retinitis that resolved within one month without antiviral therapy.
- Despite having diabetes mellitus, patients were otherwise immunocompetent with unremarkable laboratory results.
- CMV retinitis in these immunocompetent patients presented with significant anterior and vitreous inflammation.
Implications:
- CMV retinitis can occur in immunocompetent individuals, particularly those with diabetes mellitus.
- Antiviral treatment may not be necessary for CMV retinitis in immunocompetent patients.
- Further research is warranted to explore the association between CMV retinitis and diabetes mellitus.
Background:
Cytomegalovirus (CMV) retinitis usually affects severely immunosuppressed individuals. We report two immunocompetent patients who developed CMV retinitis.
Cases:
Case 1 was a 65-year-old man who was referred to us with blurred vision and floaters of 2 weeks duration in his left eye. Slit-lamp biomicroscopy showed keratic precipitates, aqueous cells, and vitreous opacity in his left eye. Funduscopic examination revealed yellow-white retinal lesions with arterial sheathing in the superotemporal midperiphery. Case 2 was a 63-year-old man who presented with a 2-week history of blurred vision in his left eye. Ophthalmologic examination of the left eye showed keratic precipitates, aqueous cells, vitreous opacity, and yellow-white lesions in the superotemporal peripheral retina. In both cases, CMV DNA was detected in the aqueous humor and therefore the diagnosis was CMV retinitis. CMV retinitis in both cases was indolent and was resolved in one month without treatment with antiviral drugs. Although both patients had diabetes mellitus, the results of their laboratory examinations were unremarkable and they were immunocompetent.
Conclusions:
Unlike CMV retinitis in immunocompromised patients, CMV retinitis in immunocompetent patients had significant anterior and vitreous inflammation but did not require antiviral treatment. A possible association between CMV retinitis and diabetes mellitus was suggested.
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