02 February 2026
: Case report
Multimodal Imaging Studies of Pigmented Paravenous Retinochoroidal Atrophy: A Case Report
Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
Yao Xu BDE 1, Feng Bai B 1, Jiahui Zhang C 2, Fu-qiang Li BC 1, Xin Pan ADEFG 1*DOI: 10.12659/AJCR.949472
Am J Case Rep 2026; 27:e949472
Figure 3 Optical coherence tomography angiography (OCTA) and spectral-domain optical coherence tomography (SD-OCT) imaging of the patient with pigmented paravenous retinochoroidal atrophy. (A) En face OCTA image of the superficial capillary layer (inner limiting membrane to inner plexiform layer) of the right eye. (B) En face OCTA image of the deep capillary layer (inner plexiform layer to outer plexiform layer) of the right eye showed substantial rarefaction. (C) En face OCTA image of the outer retinal layer (outer plexiform layer to Bruch membrane) of the right eye. (D) En face OCTA image of the choriocapillaris layer (Bruch membrane to 30 μm below) of the right eye showed several flow voids in the macular region (yellow arrows). (E) En face OCTA image of the superficial capillary layer of the left eye. (F) En face OCTA image of the deep capillary layer of the left eye showed substantial rarefaction. (G) En face OCTA image of the outer retinal layer of the left eye. (H) OCTA image of the choriocapillaris layer of the left eye showed several flow voids in the macular region (yellow arrows). (I) SD-OCT image of the right macula showed absence of the myoid zone, ellipsoid zone, and interdigitation zone, with partial preservation of the retinal pigment epithelium and choriocapillaris atrophy. (J) SD-OCT image of the left macula showed findings similar to those of the right eye.






