scholarly journals Choroidal Neovascularization Induced by Immunogenic Alteration of the Retinal Pigment Epithelium in Dengue Fever

2015 ◽  
Vol 6 (1) ◽  
pp. 18-23 ◽  
Author(s):  
Carlos Eduardo Veloso ◽  
Ursula Schmidt-Erfurth ◽  
Márcio B. Nehemy

Purpose: To report the first case of choroidal neovascularization (CNV) secondary to dengue fever. Case Report: A 54-year-old female was referred to our department with blurred vision and metamorphopsia in her left eye. Two weeks earlier, she had presented all of the classic symptoms of dengue fever including a positive serology. Her best-corrected visual acuity (BCVA) was 20/150 in the left eye. She underwent a fundus examination, fluorescein angiography (FA) and spectral domain optical coherence tomography. Results: All findings were consistent with CNV secondary to dengue fever. FA revealed a classic CNV associated with focal retinal pigment epithelium (RPE) destruction and detachment. Three consecutive monthly injections of intravitreal ranibizumab resulted in functional and anatomical improvement for as long as 6 months with a BCVA of 20/25. However, CNV recurred 2 years later, again with an improvement after ranibizumab therapy, but with persistence of a fibrovascular RPE detachment, highlighting the pathomechanism of a classic CNV formation. Conclusions: Maculopathy in dengue fever may be followed by CNV as a result of the immunologic alteration of the RPE. Physicians should be aware of this manifestation to be able to initiate adequate treatment with excellent functional and anatomical results.

2020 ◽  
pp. 112067212096202
Author(s):  
Aowang Qiu ◽  
Yan Yu ◽  
Junlong Huang ◽  
Qinghuai Liu ◽  
Yannis M Paulus ◽  
...  

Retinitis punctata albescens (RPA) is generally diagnosed by the presence of numerous clusters of white punctate lesions in the retina that progress over time and are related to several gene variants. The multifocal variant of congenital hypertrophy of the retinal pigment epithelium (CHRPE) is characterized by multiple, grouped, sharply circumscribed, pigmented spots. The PRPH2 gene encodes a photoreceptor-specific glycoprotein, which is essential for the morphogenesis of rod and cone photoreceptor outer segments. A 39-year-old Chinese female with nyctalopia, complained about blurred vision, presented a unique co-existing feature of RPA and CHRPE. Dilated fundus exam demonstrated numerous porcelain white discrete dots in both eyes and multiple, small, flat clusters of round brown to black pigmented lesions in the left eye. The full field electroretinography (ERG) showed decreased responses after standard dark adaptation and normal b-wave amplitudes after a long (4-h) dark-adapted period. A heterozygous PRPH2 splicing variant was detected in the proband. In addition, the same variant was found in her mother, her son, and her daughter. We describe a PRPH2 variant in a rare case of RPA associated with multifocal CHRPE of the same individual.


Retina ◽  
2001 ◽  
Vol 21 (3) ◽  
pp. 267-270 ◽  
Author(s):  
PANAGIOTIS G. THEODOSSIADIS ◽  
DIMITRIS N. PANAGIOTIDIS ◽  
STEFANOS G. BALTATZIS ◽  
GERASSIMOS T. GEORGOPOULOS ◽  
MICHAEL N. MOSCHOS

2014 ◽  
Vol 5 (1) ◽  
pp. 34-37 ◽  
Author(s):  
Tsuyoshi Shimoyama ◽  
Hisanori Imai ◽  
Shigeru Honda ◽  
Akira Negi

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