1型新血管化伴动脉瘤扩张的年轻女性非典型发病

Q3 Medicine

Archivos De La Sociedad Espanola De Oftalmologia Pub Date : 2024-12-01 DOI:10.1016/j.oftal.2024.07.009

M. Zamorano , B. Puerto , J. Carceller , J.J. González-López , M.S. Figueroa , F.J. Muñoz-Negrete

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引用次数: 0

摘要

1型新生血管伴动脉瘤样扩张（N1a），是一种以脉络膜血管异常为特征的视网膜疾病。临床表现为渗出性黄斑病变，伴有多发性复发性血清液色素上皮脱落。这种疾病在55-65岁的女性中更为常见。然而，我们提出了一个例外的情况下，N1a在一个26岁的妇女，谁对阿伯西普反应良好。据我们所知，这是第一例30岁以下的年轻女性感染N1a的病例。患者对三次玻璃体内注射阿伯西普的抗vegf治疗反应良好。此外，我们还提供了N1a抗vegf治疗方案的最新进展。

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Presentación atípica de neovascularización tipo 1 con dilataciones aneurismáticas en una mujer joven

Type 1 neovascularization with aneurysmal dilations (N1a), is a retinal disorder characterized by choroidal vascular abnormalities. Clinically, it is characterized by an exudative maculopathy with multiple recurrent serosanguineous pigment epithelial detachments. This disease is more common in women aged 55-65 years. However, we present an exceptional case of N1a in a 26-year-old woman, who responded favorably to aflibercept. As far as we know, this is the first case ever reported of a young woman under 30 with N1a. The patient has responded very favourably to anti-VEGF therapy with three intravitreal injections of aflibercept. Moreover, we provide an update on anti-VEGF therapeutic options for N1a.

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来源期刊

Archivos De La Sociedad Espanola De Oftalmologia Medicine-Ophthalmology

CiteScore

1.20

自引率

0.00%

发文量

109

审稿时长

78 days

期刊介绍： La revista Archivos de la Sociedad Española de Oftalmología, editada mensualmente por la propia Sociedad, tiene como objetivo publicar trabajos de investigación básica y clínica como artículos originales; casos clínicos, innovaciones técnicas y correlaciones clinicopatológicas en forma de comunicaciones cortas; editoriales; revisiones; cartas al editor; comentarios de libros; información de eventos; noticias personales y anuncios comerciales, así como trabajos de temas históricos y motivos inconográficos relacionados con la Oftalmología. El título abreviado es Arch Soc Esp Oftalmol, y debe ser utilizado en bibliografías, notas a pie de página y referencias bibliográficas.