VKH with APECED in a Two-Year-Old Child: A Rare Concomitant Diagnosis in an Unprecedented Age

被引:2
作者
Hassan, Lameece Moustafa [1 ,3 ]
Hassan, Mona M. M. [2 ]
Shady, Hend Abou [2 ]
Khedr, Dina [2 ]
机构
[1] Cairo Univ, Ophthalmol, Cairo, Egypt
[2] Cairo Univ, Pediat, Cairo, Egypt
[3] Cairo Univ, Ophthalmol, 3 Rd 217,Degla Maadi, Cairo 11431, Egypt
关键词
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome; choroiditis; exudative detachment; vitritis; Vogt Koyanagi Harada; KOYANAGI-HARADA-SYNDROME; MANAGEMENT; DISEASE;
D O I
10.1080/09273948.2023.2208212
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
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.
引用
收藏
页码:433 / 436
页数:4
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