Susac’s syndrome or catastrophic antiphospholipid syndrome?

Author:

Bucciarelli S1,Cervera R2,Martínez M3,Latorre X4,Font J1

Affiliation:

1. Department of Autoimmune Diseases, Hospital Clínic, Barcelona, Catalonia, Spain

2. Department of Autoimmune Diseases, Hospital Clínic, Barcelona, Catalonia, Spain,

3. Department of Neurology, Hospital Verge de Meritxell, Andorra la Vella, Andorra

4. Department of Internal Medicine, Hospital Verge de Meritxell, Andorra la Vella, Andorra

Abstract

Susac’s syndrome is a microangiopathic disorder of unknown pathogenesis presenting with encephalopathy, hearing loss and branch retinal artery occlusions. The term ‘catastrophic’ antiphospholipid syndrome (APS) is used to define a subset of the APS characterized by thrombotic microangiopathy with clinical evidence of three or more organ involvement developed in a short period of time. We describe a patient with typical features of Susac’s syndrome, that appeared in less than a week, in whom aPL were detected, thus fulfilling criteria for ‘probable’ catastrophic APS.

Publisher

SAGE Publications

Subject

Rheumatology

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1. Susac syndrome;Retinal and Choroidal Vascular Diseases of the Eye;2024

2. Susac’s syndrome – the crucial role of imaging tests for proper diagnosis;Annals of Agricultural and Environmental Medicine;2022-06-02

3. CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME AND POSTERIOR OCULAR INVOLVEMENT;Retina;2021-11

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