Severe Vaso-Occlusive and Ocular Decompression Retinopathy Revealing a Sickle Cell Trait in a Patient with Herpetic Uveitis.
Acetazolamide
anhydrase carbonic inhibitor
herpetic uveitis
ocular decompression retinopathy
retinal arterial occlusion
sickle cell trait
Journal
Ocular immunology and inflammation
ISSN: 1744-5078
Titre abrégé: Ocul Immunol Inflamm
Pays: England
ID NLM: 9312169
Informations de publication
Date de publication:
28 Nov 2022
28 Nov 2022
Historique:
entrez:
28
11
2022
pubmed:
29
11
2022
medline:
29
11
2022
Statut:
aheadofprint
Résumé
To describe a patient with hypertensive herpetic uveitis complicated by arterial retinal occlusions and a decompression retinopathy revealing a sickle cell trait. Case report. A 24-year-old African man presented with a hypertensive herpetic keratouveitis. A brutal lowering of the intraocular pressure (IOP) by systemic acetazolamide resulted in a ocular decompression retinopathy and multiple arterial occlusions involving the macular and the mid-periphery retina. A hemoglobin electrophoresis revealed a sickle cell trait. Under rare circumstances, vaso occlusive events can occur in patients with a sickle cell trait. We identified high IOP and acetazolamide to be responsible of an increased blood viscosity and a reduction of the vessels' caliber, resulting in sickling and arterial retinal occlusions. We recommend a thorough anamnesis and a sickle cell screening for patients of African or Mediterranean descent with acute elevated IOP, especially if they have to be treated with carbonic anhydrase inhibitors.
Identifiants
pubmed: 36442016
doi: 10.1080/09273948.2022.2147545
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM