Rodriguez Natalia, Eliott Dean, Garcia-Valenzuela Enrique, Baker John
Kresge Eye Institute, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Am J Ophthalmol. 2002 Sep;134(3):443-5. doi: 10.1016/s0002-9394(02)01570-2.
To report a case of bilateral panuveitis in a patient with hypohidrotic ectodermal dysplasia.
Interventional case report.
A 6-year-old African-American boy with hypohidrotic ectodermal dysplasia presented with pain, photophobia, and decreased vision in both eyes.
Findings included severe bilateral panuveitis with optic disk edema, macular epiretinal membrane, peripheral retinal vasculitis, and retinitis. All other known causes of panuveitis were explored and ruled out.
The abnormal development of tissues of ectodermal origin evident in hypohidrotic ectodermal dysplasia may include a predisposition to panuveitis.
报告1例患有少汗型外胚层发育不良的患者发生双侧全葡萄膜炎的病例。
介入性病例报告。
一名患有少汗型外胚层发育不良的6岁非裔美国男孩出现双眼疼痛、畏光和视力下降。
检查发现包括严重的双侧全葡萄膜炎,伴有视盘水肿、黄斑视网膜前膜、周边视网膜血管炎和视网膜炎。对所有其他已知的全葡萄膜炎病因进行了排查并排除。
少汗型外胚层发育不良中明显的外胚层来源组织的异常发育可能包括易患全葡萄膜炎的倾向。