A Review and Update on the Ophthalmic Implications of Susac Syndrome
Overview
Affiliations
Susac syndrome is a rare condition presumed to be immune-mediated occlusion of small arterial vasculature principally of the brain, inner ear, and retina. Clinically, the syndrome manifests as a pathognomonic triad of encephalopathy, hearing loss, and branch retinal artery occlusion. Early recognition and diagnosis is important as delayed treatment may be profound and result in deafness, blindness, dementia, and other neurological deficits. The plethora of imaging technology, including magnetic resonance imaging, retinal fluorescein angiography, optical coherence tomography, and optical coherence tomography angiography, allows deeper and more discrete anatomical-physiological correlation of underlying pathology, early diagnosis, and imaging biomarkers for early detection of relapse during follow-up. We highlight the current clinical classification of Susac syndrome, available investigations, treatment, and care pathways.
Successful treatment of a complete Susac syndrome in a 16-year-old boy: A case report.
Kashipazha D, Bahramy M, Razaghi M, Rahimi Z Clin Case Rep. 2024; 12(8):e9027.
PMID: 39055087 PMC: 11268951. DOI: 10.1002/ccr3.9027.
Maitray A, Kuriakose A, Rajendran A, Srinivasan K, Mahalingam M Taiwan J Ophthalmol. 2024; 14(2):271-274.
PMID: 39027075 PMC: 11254002. DOI: 10.4103/tjo.TJO-D-22-00107.
Susac syndrome in a patient with chronic myelocytic leukemia: Consequence or coincidence?.
Maleki A, Saigal K, Kera J Am J Ophthalmol Case Rep. 2024; 33:101996.
PMID: 38318442 PMC: 10839863. DOI: 10.1016/j.ajoc.2024.101996.
Susac syndrome: a case report with initial presentation of incomplete bitemporal hemianopia.
Gunaratnam C, King T, Moloney T, Boggild M, Goodwin T J Surg Case Rep. 2023; 2023(10):rjad541.
PMID: 37867919 PMC: 10587006. DOI: 10.1093/jscr/rjad541.
Susac Syndrome With Retinal Vasculitis: A Rare Case Report and Brief Review.
Sun T, Qian Y, Wang Z, Xiao Y J Clin Neurol. 2023; 19(5):495-497.
PMID: 37635426 PMC: 10471549. DOI: 10.3988/jcn.2022.0477.