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Ocul Immunol Inflamm ; 32(4): 433-436, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38412247

RESUMO

PURPOSE: To present a case of Vogt Koyanagi Harada (VKH) associated with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in a two-year-old. CASE PRESENTATION: A two-year-old type 1 diabetic with hypothyroidism presented with impaired fixation. Ocular examination revealed right vitritis, choroiditis, a hyperemic disc, and an area of exudative detachment. At the same time, there was no fundus view in the left eye, and ultrasonographic assessment revealed vitritis and a thickened choroid. Patient developed sunset glow fundus with alopecia, poliosis and vitiligo and a diagnosis of complete VKH with APECED was made. CONCLUSION: APECED is a rare endocrine disorder and has been reported to be associated with VKH twice. Likewise, VKH is commonly present in much older patients; this is the first time ever to be diagnosed in a two-year-old child.


Assuntos
Poliendocrinopatias Autoimunes , Síndrome Uveomeningoencefálica , Pré-Escolar , Feminino , Humanos , Diabetes Mellitus Tipo 1/complicações , Diabetes Mellitus Tipo 1/diagnóstico , Angiofluoresceinografia/métodos , Fundo de Olho , Poliendocrinopatias Autoimunes/diagnóstico , Poliendocrinopatias Autoimunes/complicações , Tomografia de Coerência Óptica , Ultrassonografia , Síndrome Uveomeningoencefálica/diagnóstico , Síndrome Uveomeningoencefálica/complicações , Síndrome Uveomeningoencefálica/tratamento farmacológico
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