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一例罕见的深层后葡萄肿合并黄斑裂孔视网膜脱离的双侧脉络膜视网膜缺损。

A rare case of bilateral choroidal coloboma within deep posterior staphyloma associated with macular hole retinal detachment.

机构信息

Department of Retina and Vitreous, Nethradhama Superspeciality Eye Hospital, Bangalore, Karnataka, India.

出版信息

Indian J Ophthalmol. 2019 May;67(5):699-700. doi: 10.4103/ijo.IJO_729_18.

Abstract

To report case of bilaterally symmetrical choroidal coloboma within posterior staphyloma with MHRD. This is a case report of a 50year old female presented with diminished vision in both eyes. On examination, she had Bilateral High Myopia with recent onset MHRD associated with symmetrically bilateral Choroidal Coloboma within posterior staphyloma and was operated for MHRD in left eye. Presence of choroidal coloboma within posterior staphyloma is rare and with coexisting macular hole makes pathophysiology of RD challenging to understand.

摘要

报告一例伴有后部葡萄肿的双侧对称性脉络膜缺损合并 MHRD 的病例。这是一例 50 岁女性的病例报告,她双眼视力下降。检查发现,她双眼高度近视,近期出现 MHRD,伴有双侧对称性后部葡萄肿脉络膜缺损,并在左眼接受 MHRD 手术。后部葡萄肿内脉络膜缺损较为罕见,合并黄斑裂孔使 RD 的发病机制难以理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd06/6498935/a076009df49c/IJO-67-699-g001.jpg

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