Bilateral Progressive Optic Neuropathy in a Patient with Familial Amyloid Polyneuropathy: Amyloid Deposits in Optic Nerve Head?


Por: Vela J.I., Perich S., Bulnes V., Loscos I., Baradad M.

Publicada: 10 feb 2023 Ahead of Print: 1 ene 2023
Resumen:
Familial amyloid polyneuropathy is a rare autosomal dominant hereditary disease. Optic nerve involvement is frequently observed secondary to uncontrolled glaucoma but rarely, an ischaemic optic neuropathy can occur. In this case report, we describe a patient who presented with bilateral progressive visual loss and constriction of his visual fields. Fundus examination showed intense paleness of both optic discs with elevated, poorly defined margins that seemed to be infiltrated. Fundus autofluorescence and enhanced-depth imaging optical coherence tomography ruled out the presence of optic disc drusen. Orbital magnetic resonance imaging ruled out any sign of orbital compression, inflammation or infiltration of the optic nerve. The mechanism of small vessel amyloid infiltration and a possible vessel compression by amyloid in the optic nerve head is discussed. © 2023 Taylor & Francis Group, LLC.

Filiaciones:
Vela J.I.:
 Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain

 Department of Ophthalmology, Institut Condal d’Oftalmologia, Barcelona, Spain

 Department of Surgery, Universitat Autònoma de Barcelona, Bellaterra, Spain

 Institut d´Investigació Biomèdica Sant Pau (IIB Sant Pau), Barcelona, Spain

Perich S.:
 Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain

Bulnes V.:
 Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain

Loscos I.:
 Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain

Baradad M.:
 Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain
ISSN: 01658107
Editorial
TAYLOR & FRANCIS AS, KARL JOHANS GATE 5, NO-0154 OSLO, NORWAY, Estados Unidos America
Tipo de documento: Article
Volumen: 47 Número: 3
Páginas: 164-170
WOS Id: 000937968500001
ID de PubMed: 37398503

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