[Sturge-Weber综合征中的环状脉络膜血管瘤]。

Anna Vetter, Annette Zimpfer, Björn Schneider, Andreas Erbersdobler, Tobias Brockmann, Thomas Fuchsluger, Claudia Brockmann
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引用次数: 0

摘要

我们报告了一名 19 岁的 Sturge-Weber 综合征(SWS)患者,患者右眼伴有火焰痣、继发性青光眼和青光眼性视神经萎缩。疼痛和失明的眼睛被去核。组织病理学分析显示,视神经周围有一个环形脉络膜血管瘤和一个较小的巩膜外血管瘤。分子基因检测排除了 GNA11、GNAQ 或 GNAS 突变。我们的研究阐明了这一罕见病例的临床、组织学和分子遗传学方面的问题,有助于鉴别诊断 SWS 患者的眼部疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Circumscribed choroidal hemangioma in Sturge-Weber syndrome].

We report on a 19-year-old patient with Sturge-Weber syndrome (SWS), accompanied by a Naevus flammeus, secondary glaucoma, and glaucomatous optic atrophy of the right eye. The painful and blind eye was enucleated. Histopathological analysis revealed a circumscribed choroidal hemangioma around the optic nerve and a smaller extrascleral hemangioma. Molecular genetic testing excluded GNA11, GNAQ, or GNAS mutations. Our work illuminates the clinical, histological, and molecular genetic aspects of this rare case, contributing to the differential diagnosis of ocular conditions in patients with SWS.

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