弹性假性黄瘤脉络膜新生血管的治疗:玻璃体切除和玻璃体内雷尼单抗/阿非利赛普治疗的结果- 1例报告。

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2025-05-21 eCollection Date: 2025-01-01 DOI:10.1155/crop/9286332
Kazuya Yamashita, Kento Hashizume, Yasumasa Fukuda, Rio Sato, Nobuhiro Ozawa, Hirohisa Kubono, Mari Kawamura, Kotaro Suzuki
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引用次数: 0

摘要

背景:弹性假性黄瘤(PXE)是一种影响皮肤、眼睛和血管系统的全身性疾病。它通常表现为视网膜血管样条纹(as),并可导致视力丧失,由于视网膜下新生血管和黄斑萎缩。确诊通过皮肤活检显示钙化弹性纤维或确定双等位ABCC6致病变异。该病例报告是新颖的,因为它描述了通过玻璃体切除术和玻璃体内注射雷尼单抗和阿非利塞普治疗PXE继发脉络膜新生血管(CNV)的临床过程。病例介绍:一名68岁女性,右眼视力减退。她的病史包括高血压、子宫肌瘤和多种药物过敏。眼科检查显示右眼视盘周围放射状AS及视网膜下出血。荧光素血管造影和光学相干断层扫描证实CNV和新鲜视网膜下出血。一系列的玻璃体切除术和玻璃体内注射雷尼珠单抗和阿非利塞普来控制CNV和黄斑下出血。尽管复发,随后的手术稳定了她的病情,在6年的时间里,她的右眼最佳矫正视力提高到20/125。皮肤活检证实了PXE的诊断,这是她30多年来一直忽视的疾病。结论:本病例强调了通过彻底的眼底检查早期发现AS的重要性,同时对全身状况进行全面评估。PXE患者CNV的治疗包括及时使用玻璃体内抗vegf注射和玻璃体切除联合组织纤溶酶原激活剂(tPA)来控制CNV活性和黄斑下出血。眼科医生应考虑出现特征性皮肤和眼部表现的患者的PXE,并在必要时将其转介进行皮肤科评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Managing Choroidal Neovascularization in Pseudoxanthoma Elasticum: Outcomes of Vitrectomy and Intravitreal Ranibizumab/Aflibercept Therapy-A Case Report.

Background: Pseudoxanthoma elasticum (PXE) is a systemic disorder that affects the skin, eyes, and vascular system. It commonly presents with retinal angioid streaks (ASs) and can lead to vision loss due to subretinal neovascularizations and macular atrophy. Diagnosis is confirmed through skin biopsies showing calcified elastic fibers or identifying biallelic ABCC6 pathogenic variants. This case report is novel as it describes the clinical course of choroidal neovascularization (CNV) secondary to PXE treated with vitrectomy and intravitreal ranibizumab and aflibercept injections in both eyes. Case Presentation: A 68-year-old woman presented with vision loss in her right eye. Her medical history included hypertension, uterine fibroids, and multiple drug allergies. Ophthalmic examination revealed radial AS around the optic discs and subretinal hemorrhages in the right eye. Fluorescein angiography and optical coherence tomography confirmed CNV and fresh subretinal hemorrhage. A series of vitrectomies and intravitreal injections of ranibizumab and aflibercept were performed to manage the CNV and submacular hemorrhage. Despite recurrence, subsequent surgeries stabilized her condition, improving her best-corrected visual acuity to 20/125 in the right eye over 6 years. A skin biopsy confirmed the diagnosis of PXE, a condition she had overlooked for over 30 years. Conclusions: This case emphasizes the importance of early detection of AS through thorough fundus examination, alongside comprehensive evaluation for systemic conditions. Management of CNV in PXE involves the prompt use of intravitreal anti-VEGF injections and vitrectomy with tissue plasminogen activator (tPA) for controlling CNV activity and submacular hemorrhage. Ophthalmologists should consider PXE in patients presenting with characteristic skin and eye findings and refer them for dermatological evaluation as necessary.

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