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罕见的斯特拉茨马综合征——不良预后有多教条?

Unusual Straatsma Syndrome - How dogmatic is a bad prognosis?

作者信息

Vide-Escada Ana, Prior Filipe Helena

机构信息

Integrated Responsibility Centre of Ophthalmology of Hospital Garcia de Orta EPE, Av. Torrado da Silva, 2805-267 Almada, Portugal.

Hospital das Forças Armadas/Polo de Lisboa-EMGFA, Azinhaga dos Ulmeiros, 1690-020 Lisboa, Portugal.

出版信息

Am J Ophthalmol Case Rep. 2017 Oct 7;8:71-73. doi: 10.1016/j.ajoc.2017.10.003. eCollection 2017 Dec.

DOI:10.1016/j.ajoc.2017.10.003
PMID:29260122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5731674/
Abstract

PURPOSE

To show that Straatsma Syndrome can have a good outcome and to highlight an unusual presentation of this disease.

OBSERVATIONS

A four-year-old boy presents with severe right eye amblyopia in association with high myopia, esotropia, heterochromia and extensive myelinated retinal fibers involving both temporal arcades and the optic nerve head. Right eye initial visual acuity was less than 20/400 for distance and less than R6W10 for near. Left eye examination was unremarkable. Despite the indicators for bad prognosis, intensive occlusion therapy was prescribed. Parents were strongly involved in the treatment regimen. After four months, the patient presented an unexpected good visual recovery both for distance and near, that has persisted until present. Right eye visual acuity is 20/30 with -9.00 dioptres contact lens for distance and R2W1 for near. Esotropia also improved to 12 prism dioptres. Fundoscopic alterations and heterochromia have remained stable. Spectral-domain optical coherence tomography images of the right eye showed thinner superior outer ring measurements.

CONCLUSIONS AND IMPORTANCE

Straatsma Syndrome can present with heterochromia . When strabismus is present, early surgery should be withheld. Intensive treatment of Straatsma Syndrome can yield an unexpected good result, despite initial high degree anisometropia and low vision acuity.

摘要

目的

证明斯特拉茨马综合征可取得良好预后,并强调该疾病的一种不寻常表现。

观察结果

一名4岁男孩因高度近视、内斜视、异色症以及累及双侧颞侧视网膜弓和视神经乳头的广泛视网膜神经纤维髓鞘化而出现严重右眼弱视。右眼初始远视力低于20/400,近视力低于R6W10。左眼检查无异常。尽管预后指标不佳,但仍给予强化遮盖疗法。家长积极参与治疗方案。四个月后,患者远视力和近视力均意外地得到良好恢复,且一直持续至今。右眼戴-9.00屈光度隐形眼镜时远视力为20/30,近视力为R2W1。内斜视也改善至12棱镜度。眼底改变和异色症保持稳定。右眼的频域光学相干断层扫描图像显示上方外环测量值较薄。

结论及重要性

斯特拉茨马综合征可伴有异色症。存在斜视时,应推迟早期手术。尽管初始存在高度屈光参差和低视力,但强化治疗斯特拉茨马综合征可产生意外的良好效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/03c23e544918/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/6b1628912fe4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/4b150357fd75/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/03c23e544918/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/6b1628912fe4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/4b150357fd75/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cd/5731674/03c23e544918/gr3.jpg

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