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Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report

Ocular manifestations of anemia include conjunctival pallor, retinal hemorrhages, cotton wool spots, Roth spots, subhyaloid hemorrhage, venous dilatation, disc edema, and anterior ischemic optic neuropathy (AION). Retinal arterial occlusion is a very rare complication of iron deficiency anemia. We,...

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Autores principales: Deb, Amit Kumar, Subramaniam, Swathi, Sarkar, Sandip, Suneel, Sangaraju, Elamurgan, Vignesh, Kaliaperumal, Subashini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262015/
https://www.ncbi.nlm.nih.gov/pubmed/35813796
http://dx.doi.org/10.4103/tjo.tjo_70_20
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author Deb, Amit Kumar
Subramaniam, Swathi
Sarkar, Sandip
Suneel, Sangaraju
Elamurgan, Vignesh
Kaliaperumal, Subashini
author_facet Deb, Amit Kumar
Subramaniam, Swathi
Sarkar, Sandip
Suneel, Sangaraju
Elamurgan, Vignesh
Kaliaperumal, Subashini
author_sort Deb, Amit Kumar
collection PubMed
description Ocular manifestations of anemia include conjunctival pallor, retinal hemorrhages, cotton wool spots, Roth spots, subhyaloid hemorrhage, venous dilatation, disc edema, and anterior ischemic optic neuropathy (AION). Retinal arterial occlusion is a very rare complication of iron deficiency anemia. We, hereby, report such a rare case of branch retinal artery occlusion (BRAO) occurring as a complication of iron deficiency anemia. A 49-year-old female presented with sudden painless diminution of vision in her right eye (RE) for 2 weeks with visual acuity of 20/120 in the affected eye and 20/20 in the left eye. Fundus examination of RE showed disc pallor, arteriolar attenuation, and retinal whitening at macula. Fluorescein angiography study demonstrated delayed filling of superotemporal branch of retinal artery, suggesting BRAO as the cause of vision loss. Thorough evaluation for underlying etiology revealed severe iron deficiency anemia (hemoglobin 3.9 g/dl). Her blood pressure, blood sugar profile, lipid profile, carotid Doppler, echocardiogram, coagulation profile, and immunological workup were all unremarkable. She was treated with packed cell transfusion and oral iron supplementation, and her vision improved to 20/40 at 1-month follow-up. Retinal vascular occlusions can occur rarely in iron deficiency anemia, and therefore anemia should be considered, while evaluation of vascular occlusion – specially in those with associated conjunctival pallor as in our case.
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spelling pubmed-92620152022-07-08 Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report Deb, Amit Kumar Subramaniam, Swathi Sarkar, Sandip Suneel, Sangaraju Elamurgan, Vignesh Kaliaperumal, Subashini Taiwan J Ophthalmol Case Report Ocular manifestations of anemia include conjunctival pallor, retinal hemorrhages, cotton wool spots, Roth spots, subhyaloid hemorrhage, venous dilatation, disc edema, and anterior ischemic optic neuropathy (AION). Retinal arterial occlusion is a very rare complication of iron deficiency anemia. We, hereby, report such a rare case of branch retinal artery occlusion (BRAO) occurring as a complication of iron deficiency anemia. A 49-year-old female presented with sudden painless diminution of vision in her right eye (RE) for 2 weeks with visual acuity of 20/120 in the affected eye and 20/20 in the left eye. Fundus examination of RE showed disc pallor, arteriolar attenuation, and retinal whitening at macula. Fluorescein angiography study demonstrated delayed filling of superotemporal branch of retinal artery, suggesting BRAO as the cause of vision loss. Thorough evaluation for underlying etiology revealed severe iron deficiency anemia (hemoglobin 3.9 g/dl). Her blood pressure, blood sugar profile, lipid profile, carotid Doppler, echocardiogram, coagulation profile, and immunological workup were all unremarkable. She was treated with packed cell transfusion and oral iron supplementation, and her vision improved to 20/40 at 1-month follow-up. Retinal vascular occlusions can occur rarely in iron deficiency anemia, and therefore anemia should be considered, while evaluation of vascular occlusion – specially in those with associated conjunctival pallor as in our case. Wolters Kluwer - Medknow 2021-01-07 /pmc/articles/PMC9262015/ /pubmed/35813796 http://dx.doi.org/10.4103/tjo.tjo_70_20 Text en Copyright: © 2021 Taiwan J Ophthalmol https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Deb, Amit Kumar
Subramaniam, Swathi
Sarkar, Sandip
Suneel, Sangaraju
Elamurgan, Vignesh
Kaliaperumal, Subashini
Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title_full Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title_fullStr Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title_full_unstemmed Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title_short Branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: A rare case report
title_sort branch retinal artery occlusion as an initial ocular manifestation of severe iron deficiency anemia: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262015/
https://www.ncbi.nlm.nih.gov/pubmed/35813796
http://dx.doi.org/10.4103/tjo.tjo_70_20
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