Susac syndrome (SS) is a rare microangiopathy that involves arterioles of the brain, retina, and cochlea. Diagnosis is extremely difficult because of the rarity of the disease and because the signs and symptoms often occur at different times. Multidisciplinary approaches and multimodal images are mandatory for diagnosis and prompt therapy. In this report, we describe a case of SS and the application of multimodal retinal imaging to evaluate the ophthalmologic changes and to confirm diagnosis. Early diagnosis and therapy based on the associations of steroids and immunosuppressants are necessary to limit the sequelae of the disease. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Bagaglia, S.A., Passani, F., Oliverio, G.W., Inferrera, L., Menna, F., Meduri, A., et al. (2021). Multimodal imaging in Susac syndrome: A case report and literature review. INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 18(7), 1-6 [10.3390/ijerph18073435].
Multimodal imaging in Susac syndrome: A case report and literature review
Mazzotta C.
2021-01-01
Abstract
Susac syndrome (SS) is a rare microangiopathy that involves arterioles of the brain, retina, and cochlea. Diagnosis is extremely difficult because of the rarity of the disease and because the signs and symptoms often occur at different times. Multidisciplinary approaches and multimodal images are mandatory for diagnosis and prompt therapy. In this report, we describe a case of SS and the application of multimodal retinal imaging to evaluate the ophthalmologic changes and to confirm diagnosis. Early diagnosis and therapy based on the associations of steroids and immunosuppressants are necessary to limit the sequelae of the disease. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.File | Dimensione | Formato | |
---|---|---|---|
Multimodal Imaging in Susac Syndrome-Bagaglia-2021.pdf
accesso aperto
Descrizione: Articolo
Tipologia:
PDF editoriale
Licenza:
Creative commons
Dimensione
9.93 MB
Formato
Adobe PDF
|
9.93 MB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/1178185