Your browser doesn't support javascript.
loading
Systemic Amyloidosis and Extraocular Muscle Deposition.
Shah, Veeral S; Cavuoto, Kara M; Capo, Hilda; Grace, Sara F; Dubovy, Sander R; Schatz, Norman J.
Afiliação
  • Shah VS; Department of Ophthalmology (VS), Texas Children's Hospital, Baylor College of Medicine, Houston, Texas; Department of Ophthalmology (KMC, HC, SFG, SRD, NJS), Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.
J Neuroophthalmol ; 36(2): 167-73, 2016 06.
Article em En | MEDLINE | ID: mdl-26967574
Isolated amyloid deposition in an extraocular muscle is a rare event but can be a presenting feature of systemic amyloidosis. A 67-year-old woman with an acquired exotropia and hypertropia was found to have unilateral diffuse extraocular muscle enlargement on magnetic resonance imaging. Owing to the progressive nature of her strabismus and the negative laboratory testing for thyroid disease, she underwent an extraocular muscle biopsy that revealed amyloid deposition. Further workup demonstrated a monoclonal gammopathy consistent with systemic amyloidosis. This case demonstrates the need to consider amyloidosis in the differential diagnosis of patients presenting with an atypical acquired strabismus. We review other reports of isolated amyloid deposition in extraocular muscles and its association with systemic amyloidosis, emphasizing the importance of the ophthalmologist in the early recognition of this disease to prevent irreversible, life-threatening end organ damage.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estrabismo / Amiloidose / Músculos Oculomotores Tipo de estudo: Diagnostic_studies Limite: Aged / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estrabismo / Amiloidose / Músculos Oculomotores Tipo de estudo: Diagnostic_studies Limite: Aged / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article