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Panretinal acute multifocal placoid pigment epitheliopathy: a novel posterior uveitis syndrome with HLA-A3 and HLA-C7 association

机译:全视网膜急性多发性乳突色素上皮病:一种新的后葡萄膜炎综合征与HLA-A3和HLA-C7关联

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The purpose of this study is to report a previously undescribed clinical entity resembling acute posterior multifocal placoid pigment epitheliopathy (APMPPE) but with an atypical, panretinal and diffuse presentation in young patients with an HLA-A3 and HLA-C7 association. We describe a cluster of three, young, healthy patients who experienced acute visual loss, aged 16 through 27 years exhibiting an unusual clinical entity over an 8-month period. Our patients demonstrated a unique presentation with acute retinal lesions similar to APMPPE but had widespread presentation of multiple lesions in the peripheral retina. All three of our patients exhibited an acute loss of vision, two of them bilaterally. Ophthalmoscopy and fundus photography demonstrated a diffuse distribution of lesions located extensively throughout the retina. On fluorescein angiography, the lesions showed a characteristic ‘blocking early and staining late’ pattern similar to APMPPE. The average duration of activity was 6 weeks (range 4 to 8 weeks), and there were no recurrences and good visual prognosis. HLA-A3 and HLA-C7 was noted in 100% of the patients. Ocular coherence tomography during the acute stage in one patient demonstrated thickening at the RPE layer. To our knowledge, this cluster of young patients represents a previously undescribed clinical entity, with clinical features similar to APMPPE, relentless placoid chorioretinitis and ampiginous. Due to the diffuse distributions of the active lesions, the acute clinical course without recurrences, good visual prognosis, and HLA-A3/C7 association, we believe it to be distinct from these other white dot syndromes. All three patients experienced preceding viral-like prodrome which, when combined with major histocompatibility commonalities, may predispose these individuals to an immune response. We call this entity panretinal acute multifocal placoid pigment epitheliopathy or PAMPPE.
机译:这项研究的目的是报告以前没有描述过的类似于急性后方多灶性乳突色素上皮病(APMPPE)的临床实体,但在具有HLA-A3和HLA-C7关联的年轻患者中具有非典型,全视网膜和弥漫性表现。我们描述了一组三名年轻,健康的患者,他们经历了急性视力丧失,年龄在16至27岁之间,在8个月内表现出异常的临床症状。我们的患者表现出独特的急性视网膜病变表现,类似于APMPPE,但周围视网膜多处广泛表现病变。我们的所有三名患者均表现出急性视力丧失,其中两人双侧。眼底镜检查和眼底照相显示病变广泛分布于整个视网膜。在荧光素血管造影上,病变表现出类似于APMPPE的特征性“早期阻塞和晚期染色”模式。平均活动时间为6周(4至8周),无复发,视觉预后良好。在100%的患者中注意到HLA-A3和HLA-C7。一名患者在急性期的眼相断层扫描显示RPE层增厚。据我们所知,这群年轻患者代表了一个以前未曾描述过的临床实体,其临床特征类似于APMPPE,无情的乳突脉络膜视网膜炎和明显的。由于活动性病变的扩散分布,无复发的急性临床病程,良好的视觉预后以及HLA-A3 / C7关联,我们认为它与这些其他白点综合征不同。所有三名患者均经历过病毒样前驱病,当与主要组织相容性共同点相结合时,可能使这些人容易发生免疫反应。我们称这种实体为全视网膜急性多灶性乳突色素上皮病或PAMPPE。

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