6岁男童急性双侧浆液性视网膜脱离伴自发消退。

GMS ophthalmology cases Pub Date : 2020-08-25 eCollection Date: 2020-01-01 DOI:10.3205/oc000164
Sophie Van Camp, Steffi Vande Walle, Ingele Casteels, Julie Jacob, Cathérine Cassiman, Carine Wouters, Pieter-Paul Schauwvlieghe
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引用次数: 0

摘要

一个健康的6岁男孩表现为急性双侧视力丧失,血管拱廊和脉络膜增厚之间的多发性浆液性视网膜脱离。几个星期后,问题自然得到了解决。我们假设该患者的临床症状提示急性渗出性多形性黄斑病变(AEPVM)或可能是Vogt-Koyanagi-Harada (VKH)病的非典型表现。我们认为这是由脉络膜水平的自身免疫介导的炎症细胞激活引起的,由未知的触发因素诱导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy.

Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy.

Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy.

Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy.

A healthy 6-year-old boy presented with acute bilateral vision loss, multiple serous retinal detachments between the vascular arcades and a thickened choroid. Spontaneous resolution occurred over several weeks. We hypothesize that the clinical constellation in our patient is suggestive of acute exudative polymorphous vitelliform maculopathy (AEPVM) or might be an atypical presentation of Vogt-Koyanagi-Harada (VKH) disease. We propose that it was caused by an autoimmune-mediated activation of inflammatory cells at the level of the choroid, induced by an unknown trigger.

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