以急性后极部多灶性扁平状色素上皮病变为表现的肉芽肿性前葡萄膜炎。

Granulomatous anterior uveitis presenting with acute posterior multifocal placoid pigment epitheliopathy.

作者信息

Alvi N P, Fishman G A

机构信息

Department of Ophthalmology and Visual Sciences, University of Illinois, Chicago College of Medicine, USA.

出版信息

Doc Ophthalmol. 1995;89(4):347-53. doi: 10.1007/BF01203710.

DOI:10.1007/BF01203710

PMID:7493536

Abstract

Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) has been described as a posterior segment inflammatory disorder of young adults of unknown etiology. Granulomatous anterior uveitis in association with APMPPE has only rarely been reported in the literature. We report a patient who presented with clinical and angiographic findings consistent with APMPPE in addition to granulomatous anterior uveitis with mutton-fat keratic precipitates and Koeppe nodules. This latter finding has not been emphasized as a possible feature of APMPPE.

摘要

急性后极部多灶性鳞状色素上皮病变（APMPPE）被描述为病因不明的年轻成年人后段炎症性疾病。文献中仅有罕见报道称APMPPE合并肉芽肿性前葡萄膜炎。我们报告1例患者，其临床和血管造影表现符合APMPPE，同时伴有肉芽肿性前葡萄膜炎，出现羊脂状角膜后沉着物和科佩结节。后一发现尚未被强调为APMPPE的可能特征。