Development of Superficial Thrombophlebitis and Subsequent Central Retinal Vein Occlusion Occurring in a Patient Receiving IVIg for Ocular Pemphigoid

IVIg can effectively control severe oMMP but may increase the risk of thromboembolic events in predisposed individuals. Recurrent STP during IVIg therapy may serve as an early indicator of a more serious vascular complication, such as CRVO. Recognizing and investigating hypercoagulability in these patients is critical for preventing irreversible vision loss and guiding safer therapeutic strategies.

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Publication Details

Journal
Ocular Immunology and Inflammation
Published
2025-08-28
DOI
https://doi.org/10.1080/09273948.2025.2553871
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
Field-Weighted Citation Impact
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article

Development of Superficial Thrombophlebitis and Subsequent Central Retinal Vein Occlusion Occurring in a Patient Receiving IVIg for Ocular Pemphigoid

Guangxu Tu, Elmer Y. Tu, Kyle T. Amber, M Mihăilescu et al.
Ocular Immunology and Inflammation
Autoimmune Bullous Skin Diseases
article

Development of Superficial Thrombophlebitis and Subsequent Central Retinal Vein Occlusion Occurring in a Patient Receiving IVIg for Ocular Pemphigoid

Guangxu Tu, Elmer Y. Tu, Kyle T. Amber, M Mihăilescu, Kevin M. Truong-Balderas
article en

Abstract

IVIg can effectively control severe oMMP but may increase the risk of thromboembolic events in predisposed individuals. Recurrent STP during IVIg therapy may serve as an early indicator of a more serious vascular complication, such as CRVO. Recognizing and investigating hypercoagulability in these patients is critical for preventing irreversible vision loss and guiding safer therapeutic strategies.

Ocular Immunology and InflammationVol. 33(9)
Rush University Medical Center (US), Illinois College (US), New York Eye and Ear Infirmary (US), University of Illinois Chicago (US)
Openalex Percentile: Top 68%
Autoimmune Bullous Skin Diseases
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