Ophthalmic Manifestations as First Presenting Sign of Evans Syndrome

Author:

Mazharuddin Anam A.1,Rehmani Ahmad1ORCID,Puthenparambil Larry2,Alappatt John J.3,Lee Wen-Hsiang1

Affiliation:

1. University of Texas Medical Branch, Galveston, TX, USA

2. Eye Center of Texas, Webster, TX, USA

3. Houston Retina Associates, Webster, TX, USA

Abstract

Purpose: This work reports a case of Evans syndrome first presenting with ophthalmic signs. Methods: A 27-year-old previously healthy man presented with headaches and bilateral blurred vision for 2 weeks. The visual acuity was 20/30-1 and 20/60-2 in the right eye and left eye, respectively. A fundus examination revealed Roth spots, diffuse multilayer retinal hemorrhages in the macula and periphery, and tortuous vessels in both eyes. Optical coherence tomography showed a disrupted foveal contour from intraretinal fluid and hemorrhage in both eyes. Fluorescein angiography demonstrated dilated and tortuous vessels with scattered blocking defects from hemorrhages. Results: A workup revealed warm hemolytic anemia with severe thrombocytopenia consistent with the diagnosis of Evans syndrome. Conclusions: Evans syndrome is a rare blood dyscrasia that can first present as subacute vision loss and should be added to the differential of diffuse bilateral retinal hemorrhages spanning a multitude of retinal layers.

Publisher

SAGE Publications

Subject

General Medicine

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