| Autor: |
Meyer, Benjamin I., Liao, Albert, Sanda, Gregory E., Craven, Caroline, Wells, Jill R., Hendrick, Andrew M., Yan, Jiong, Jain, Nieraj |
| Předmět: |
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| Zdroj: |
Graefe's Archive of Clinical & Experimental Ophthalmology; Mar2024, Vol. 262 Issue 3, p777-788, 12p |
| Abstrakt: |
Purpose: To evaluate the clinical characteristics of congenital rubella retinopathy (CRR) with modern fundus imaging. Methods: Single-center case series. Eleven patients (2005–2020) at the Emory Eye Center with known or presumed CRR. Trained image readers reviewed fundus imaging (color fundus photography, widefield pseudocolor imaging, near-infrared reflectance imaging, autofluorescence imaging, and spectral-domain optical coherence tomography) for pre-specified features suggestive of CRR. Results: Eleven patients with confirmed (63.6%) or presumed (36.3%) CRR were identified. All were female with median (range) age of 53 (35–67) years. Six (54.5%) were born during the 1964–1965 United States rubella epidemic. All had congenital hearing loss. Two (18.2%) had a congenital heart defect. Eleven (50.0%) eyes had salt-and-pepper retinal pigmentary changes. Twenty-two eyes (100.0%) had irregularly distributed regions of speckled hypoautofluorescence. One eye (4.5%) had a presumed macular neovascularization. Conclusion: Modern fundus imaging demonstrates characteristic features of CRR, even when pigmentary changes are not readily apparent on examination. Widefield autofluorescence findings of irregularly distributed speckled hypoautofluorescence are particularly revealing. This series of newly diagnosed adults with CRR may represent the milder end of the phenotypic spectrum of this condition, highlighting imaging findings that may aid in diagnostically challenging cases of CRR. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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