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一例因过熟期白内障导致晶状体核脱位患者自发性全层黄斑裂孔形成与闭合:病例报告

Spontaneous full thickness macular hole development and closure in a patient with nucleus dislocation due to hypermature cataract: a case report.

作者信息

Petrovic Pajic Sanja, Lumi Xhevat, Schollmayer Petra, Hawlina Marko

机构信息

Sanja Petrovic Pajic, Clinic for Eye Diseases, Clinical Center of Serbia, Pasterova 2, 11000 Belgrade, Serbia,

出版信息

Croat Med J. 2020 Aug 31;61(4):366-370. doi: 10.3325/cmj.2020.61.366.

Abstract

Spontaneous posterior capsule rupture with lens-nucleus dislocation is a very rare entity, as is the development and spontaneous closure of a full thickness macular hole (FTMH) after vitrectomy. The occurrence of these two entities in one eye has not been previously described. A 79-year-old woman was referred because of the right eye intermittent pain and progressive visual loss. Best corrected visual acuity (BCVA) with correction for aphakia was 20/20. Intraocular pressure was normal with therapy. The cornea, anterior chamber, and vitreous were clear. Gonioscopy was normal. The capsular bag was clear, with rolled-up anterior and posterior lens capsule, and the nucleus dislocated in the vitreous. As surgery waiting time was prolonged due to administrative problems, the patient's intraocular pressure (IOP) increased and cystoid macular edema (CME) with lamellar macular hole developed. The patient underwent pars plana vitrectomy with endophacofragmentation and epiretinal membrane peeling. Postoperative optical coherence tomography was normal, BCVA was 20/40, and IOP was normal with topical therapy. One month after surgery, the eye was without signs of inflammation and IOP started rising in spite of maximum therapy. CME reoccurred and progressed to a FTMH, which started closing spontaneously in one month. One year after surgery, IOP normalized and FTMH closed completely. A dislocated crystalline lens in a quiet eye with normal BCVA, which rapidly developed into intractable glaucoma and FTMH, is an unusual finding. The deterioration was followed by spontaneous IOP normalization and macular hole closure. Such unexpected disease course, suggesting a possible autoimmune reaction, has not yet been described.

摘要

自发性后囊破裂伴晶状体核脱位是一种非常罕见的情况,玻璃体切除术后全层黄斑裂孔(FTMH)的发生及自发闭合也是如此。此前尚未有过一只眼睛同时出现这两种情况的报道。一名79岁女性因右眼间歇性疼痛和视力进行性下降前来就诊。无晶状体矫正后的最佳矫正视力(BCVA)为20/20。经治疗后眼压正常。角膜、前房和玻璃体清晰。房角镜检查正常。晶状体囊袋清晰,前后晶状体囊卷起,晶状体核脱位至玻璃体。由于行政问题手术等待时间延长,患者眼压升高,出现伴有板层黄斑裂孔的黄斑囊样水肿(CME)。患者接受了玻璃体切割联合晶状体超声乳化碎核及视网膜前膜剥除术。术后光学相干断层扫描正常,BCVA为20/40,局部治疗后眼压正常。术后1个月,术眼无炎症迹象,但尽管进行了最大剂量治疗,眼压仍开始升高。CME复发并进展为FTMH,1个月后开始自发闭合。术后1年,眼压恢复正常,FTMH完全闭合。在一只BCVA正常且安静的眼中出现脱位的晶状体,迅速发展为难治性青光眼和FTMH,这是一个不寻常的发现。病情恶化后眼压自发恢复正常,黄斑裂孔闭合。这种意想不到的病程,提示可能存在自身免疫反应,此前尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d326/7480756/93d7bed2a909/CroatMedJ_61_0366-F1.jpg

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