Incidental Unilateral Retinal Vessel Findings and Its Consequences

Introduction

Peripheral retinal vascular abnormalities may present as difficult diagnostic challenges since the findings are not pathognomonic clinically or on imaging. This retrospective case report highlights this difficulty and shows the process of stepwise exclusion of differential diagnoses.

Publikationsverlauf

Eingereicht: 19. Oktober 2022

Angenommen: 16. Februar 2023

Artikel online veröffentlicht:
25. April 2023

• References

• 1 Abdalla Elsayed MEA, Mura M, Al Dhibi H. et al. Sickle cell retinopathy. A focused review. Graefes Arch Clin Exp Ophthalmol 2019; 257: 1353-1364
• 2 Schmidt D, Pache M, Schumacher M. The congenital unilateral retinocephalic vascular malformation syndrome (Bonnet-Dechaume-Blanc syndrome or Wyburn-Mason syndrome): review of the literature. Surv Ophthalmol 2008; 53: 227-249
• 3 Schatz H, Chang LF, Ober RR. et al. Central retinal vein occlusion associated with retinal arteriovenous malformation. Ophthalmology 1993; 100: 24-30
• 4 Gilmour DF. Familial exudative vitreoretinopathy and related retinopathies. Eye (Lond) 2015; 29: 1-14
• 5 Li Y, Peng J, Li J. et al. The characteristics of digenic familial exudative vitreoretinopathy. Graefes Arch Clin Exp Ophthalmol 2018; 256: 2149-2156
• 6 Boonstra FN, van Nouhuys CE, Schuil J. et al. Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy. Invest Ophthalmol Vis Sci 2009; 50: 4379-4385