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怀伯恩-梅森综合征:一个叙事审查

Yasmin Shameem¹, Saleha Irshad¹, Nimrah Mirza¹

¹Paediatrics, Anglia Ruskin University, Chelmsford, GBR.

|September 30, 2024

概括

怀伯恩-梅森综合征是一种罕见的先天性疾病,涉及视网膜和大脑的动脉静脉形 (AVM). 管理通常是保守的,但对于高风险的内AVM来说,考虑进行干预.

科学领域:

血管医学血管医学
眼科医生眼科眼科
神经学神经学

背景情况:

怀伯恩-梅森综合征是一种罕见的先天性疾病.
它的特点是视网膜,大脑和皮肤中的动脉静脉形 (AVM).
胚胎血管异常的结果,具有不同的临床表现.

研究的目的:

审查怀伯恩-梅森综合征的诊断,管理和治疗.
强调多学科方法的重要性.
讨论新兴的治疗策略.

主要方法:

审查关于怀伯恩-梅森综合征的现有文献.
重点是诊断成像技术,如OCT和脑血管学.
讨论保守的和干预的管理策略.

主要成果:

怀伯恩-梅森综合征呈现出广泛的严重程度,分为三组.
诊断依赖于成像;OCT和脑血管造影是关键.
保守的管理是典型的,对AVM的干预超过每年2.2%的破裂风险.

结论:

涉及眼科医生,神经科医生和干预放射科医生的多学科方法至关重要.
定期监测无症状的AVM对于最佳结果至关重要.
新兴疗法为怀伯恩-梅森综合征提供了新的治疗途径.

关键词:

这是一种动脉静脉形形.波内特 - 贝 - 布朗综合征拉塞莫斯的血管瘤视网膜脑血管形综合征视网膜脑血管形综合征怀伯恩 - 梅森综合征

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