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成人发病型贝斯特罗病误诊为中心性浆液性脉络膜视网膜病变。

Adult-onset bestrophinopathy mistaken as central serous chorioretinopathy.

机构信息

Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.

Department of Ophthalmology, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio, USA.

出版信息

Ophthalmic Genet. 2022 Aug;43(4):476-480. doi: 10.1080/13816810.2022.2053994. Epub 2022 Mar 21.

Abstract

PURPOSE

To highlight cases of adult-onset bestrophinopathy mistaken as central serous chorioretinopathy (CSCR).

METHODS

Retrospective case series.

RESULTS

Two unrelated adult males (54 years old and 43 years old) with serous macular detachments were managed as CSCR. One had been treated with intraocular injections and oral mineralcorticoid inhibitors. Independently, each had an 8-year-old son who presented with classic Best disease, which raised suspicion for bestrophinopathy in their fathers. Bestrophin sequencing confirmed each son to be heterozygous for a pathogenic variant, and targeted testing confirmed each respective father to harbor the same heterozygous pathogenic variant as his son. Electro-oculography of the first father-son pair confirmed decreased Arden ratios. Review of multimodal imaging of the adult patients revealed a hyper-autofluorescent edge surrounding a serous macular detachment by short-wave autofluorescence and shaggy photoreceptors on the overlying edge of serous detachments by optical coherence tomography.

DISCUSSION

Adult-onset bestrophinopathy can be mistaken as CSCR. Multimodal imaging findings, examination of potentially affected family members, electrophysiology, and genetic testing facilitate the correct diagnosis.

摘要

目的

强调将成人发病的钙敏感受体病误诊为中心性浆液性脉络膜视网膜病变(CSCR)的病例。

方法

回顾性病例系列。

结果

两名无关联的成年男性(54 岁和 43 岁)出现浆液性黄斑脱离,被误诊为 CSCR。其中一名曾接受过眼内注射和口服盐皮质激素抑制剂治疗。每位患者均有一名 8 岁的儿子,表现为典型的 Best 病,这引起了他们父亲钙敏感受体病的怀疑。钙敏感受体基因测序证实每个儿子均为杂合致病性变异,靶向检测证实各自的父亲与其儿子携带相同的杂合致病性变异。第一对父子的眼电图证实 Arden 比值降低。对成年患者的多模态成像进行回顾性分析,发现短波自动荧光显示浆液性黄斑脱离周围有高自发荧光边缘,光相干断层扫描显示浆液性脱离的上覆边缘有绒毛状光感受器。

讨论

成人发病的钙敏感受体病可能被误诊为 CSCR。多模态成像表现、对可能受影响的家庭成员的检查、电生理学和基因检测有助于明确诊断。

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