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色素性视网膜变性与科茨病:病例研究

Pigmentary retinal degeneration and Coats' disease: a case study.

作者信息

Arrigg P G, Lahav M, Hutchins R K, Weiter J J

机构信息

Tufts-New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts.

出版信息

Ophthalmic Surg. 1988 Jun;19(6):432-6.

PMID:3419781
Abstract

We report a 22-year-old Hispanic man with familial congenital nystagmus, iris transillumination, and pigmentary retinal anomalies with subretinal fatty exudates similar to those seen in Coats' disease. Direct treatment of the telangiectatic vessels with cryotherapy caused a subretinal hemorrhage. We therefore recommend surrounding the area of abnormal vessels (posterior to vessels and between vessels and ora serrata) with cryotherapy to reverse the formation of the vascular anomalies.

摘要

我们报告了一名22岁的西班牙裔男性,患有家族性先天性眼球震颤、虹膜透照以及视网膜色素异常,伴有视网膜下脂肪性渗出物,类似于科茨病所见。用冷冻疗法直接治疗毛细血管扩张性血管导致了视网膜下出血。因此,我们建议用冷冻疗法包围异常血管区域(血管后方以及血管与锯齿缘之间),以逆转血管异常的形成。

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