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Peripheral bright streaks in tuberous sclerosis.
Eliesersdóttir, Torgerð Hentze; Holm, Elin; Eckmann-Hansen, Christina; Torm, Marie Wistrup; Belmouhand, Mohamed; Larsen, Michael.
Afiliação
  • Eliesersdóttir TH; Department of Ophthalmology, Landssjúkrahúsið, Tórshavn, Faroe Islands.
  • Holm E; Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
  • Eckmann-Hansen C; Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
  • Torm MW; Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
  • Belmouhand M; Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
  • Larsen M; Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
Am J Ophthalmol Case Rep ; 22: 101050, 2021 Jun.
Article em En | MEDLINE | ID: mdl-33732948
ABSTRACT

PURPOSE:

To describe the finding of bright hyperautofluorescent streaks in the peripheral retina in tuberous sclerosis. OBSERVATIONS A woman with a pathogenic TSC1 mutation and cutaneous manifestations of tuberous sclerosis underwent fundus examination and was found to have a cluster of thin, yellowish streaks in the inferior peripheral fundus of her left eye. The streaks were hyperautofluorescent in blue light and associated with irregular thickening of the photoreceptor-pigment epithelium complex on optical coherence tomography. CONCLUSIONS AND IMPORTANCE The cluster of outer retinal abnormalities in a sector of the peripheral retina in one eye of a TSC1 patient has features in common with the more centrally located and less numerous lesions called achromatic patches. The resemblance of the streak pattern with the pattern of hypoautofluorescence in X-linked retinopathies suggests that the streaks may represent a clone of cells derived from a single somatic mutation in TSC1. The identification of this lesion type expands the scope of conditions that can be diagnosed by fundus imaging.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Am J Ophthalmol Case Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Am J Ophthalmol Case Rep Ano de publicação: 2021 Tipo de documento: Article