• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

葡萄牙家族性淀粉样变性ATTR V30M 患者玻璃体淀粉样变性的复发和再次手术干预的需求。

Recurrence of vitreous amyloidosis and need of surgical reintervention in Portuguese patients with familial amyloidosis ATTR V30M.

机构信息

Department of Ophthalmology, Amyloid Research Center, Santo Antonio General Hospital, Porto, Portugul.

出版信息

Retina. 2011 Jul-Aug;31(7):1373-7. doi: 10.1097/IAE.0b013e318203c0c2.

DOI:10.1097/IAE.0b013e318203c0c2
PMID:21358362
Abstract

PURPOSE

Vitreous amyloid deposits are one of the most common ocular manifestations of familial amyloidosis ATTR V30M (FAP-I), which can be the only manifestation of the disease and can appear even after liver transplantation. Removal by vitrectomy is usually performed, but vitreous amyloid recurrence has been frequently reported. This study was undertaken to evaluate the recurrence of vitreous amyloidosis and its relationship with the degree of previous vitreous removal.

METHODS

Fifty-four vitrectomized eyes from 32 patients with FAP-I were evaluated in the course of a follow-up period of 30.7 ± 17.2 months (range, 8-78; median = 30 months). An extensive, as possible, vitrectomy with indentation was performed in 41 eyes (complete), and in the others 13 eyes only a vitrectomy without indentation (incomplete) was performed. The parameters evaluated were the incidence of amyloid deposits and visual outcomes.

RESULTS

A noteworthy visual acuity gain was observed, although a few patients had a subsequent decrease of visual acuity related to new vitreous amyloid deposition in the visual axis. These new amyloid deposits did not occur in eyes that had undergone extensive vitreous removal, but only in nonextensive vitrectomized eyes (P < 0.001).

CONCLUSION

Recurrence of amyloid deposition only occurred in nonextensive vitrectomized eyes and represents a false recurrence associated with incomplete vitrectomy.

摘要

目的

玻璃体内淀粉样沉积物是家族性淀粉样变性ATTR V30M(FAP-I)的最常见眼部表现之一,它可能是该疾病的唯一表现,甚至在肝移植后也会出现。通常通过玻璃体切除术进行清除,但已频繁报道玻璃体内淀粉样沉积物的复发。本研究旨在评估玻璃体内淀粉样变性的复发及其与先前玻璃体切除程度的关系。

方法

在 30.7±17.2 个月(范围,8-78;中位数=30 个月)的随访期间,评估了 32 例 FAP-I 患者的 54 只玻璃体切除眼。在 41 只眼中进行了广泛的(尽可能的)玻璃体切除术并进行了内压,而在其余 13 只眼中仅进行了无内压的玻璃体切除术(不完全)。评估的参数是淀粉样沉积物的发生率和视力结果。

结果

观察到显著的视力提高,尽管少数患者的视力随后下降,这与视轴上新的玻璃体内淀粉样沉积物有关。这些新的淀粉样沉积物仅发生在未进行广泛玻璃体切除的眼中,而不在广泛玻璃体切除的眼中发生(P<0.001)。

结论

淀粉样沉积物的复发仅发生在不完全玻璃体切除的眼中,代表与不完全玻璃体切除术相关的假复发。

相似文献

1
Recurrence of vitreous amyloidosis and need of surgical reintervention in Portuguese patients with familial amyloidosis ATTR V30M.葡萄牙家族性淀粉样变性ATTR V30M 患者玻璃体淀粉样变性的复发和再次手术干预的需求。
Retina. 2011 Jul-Aug;31(7):1373-7. doi: 10.1097/IAE.0b013e318203c0c2.
2
Vitreous surgery impact in glaucoma development in liver transplanted familial amyloidosis ATTR V30M Portuguese patients.玻璃体手术对肝移植家族性淀粉样变性ATTR V30M 葡萄牙患者青光眼发展的影响。
Amyloid. 2012 Sep;19(3):146-51. doi: 10.3109/13506129.2012.710669. Epub 2012 Aug 3.
3
Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.一名转甲状腺素蛋白基因存在TTR Val30Gly突变的患者发生眼软脑膜淀粉样变性。
Ophthalmology. 2007 Nov;114(11):e33-7. doi: 10.1016/j.ophtha.2007.07.007.
4
25-gauge vitrectomy to treat ocular complications of familial amyloid polyneuropathy.25G玻璃体切除术治疗家族性淀粉样多神经病的眼部并发症。
J Glaucoma. 2007 Jan;16(1):169-70. doi: 10.1097/01.ijg.0000212291.85669.21.
5
Impact of liver transplantation on the natural history of oculopathy in Portuguese patients with transthyretin (V30M) amyloidosis.肝移植对葡萄牙转甲状腺素蛋白(V30M)淀粉样变性眼病患者自然病程的影响。
Amyloid. 2015 Mar;22(1):31-5. doi: 10.3109/13506129.2014.989318. Epub 2014 Dec 5.
6
Vitreous opacities and outcome of vitreous surgery in patients with familial amyloidotic polyneuropathy.家族性淀粉样多神经病患者的玻璃体混浊及玻璃体手术结果
Am J Ophthalmol. 2003 Feb;135(2):188-93. doi: 10.1016/s0002-9394(02)01838-x.
7
Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases.遗传性转甲状腺素蛋白(ATTR V30M)携带者的眼科表现:513例病例综述
Amyloid. 2015;22(2):117-22. doi: 10.3109/13506129.2015.1015678. Epub 2015 Jun 22.
8
Immunostaining images of vitreous transthyretin amyloid.玻璃体转甲状腺素蛋白淀粉样变的免疫染色图像。
Can J Ophthalmol. 2015 Oct;50(5):384-7. doi: 10.1016/j.jcjo.2015.06.007.
9
Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights.玻璃体内淀粉样变性:眼部、全身和遗传的新见解。
Ophthalmology. 2017 Jul;124(7):1014-1022. doi: 10.1016/j.ophtha.2017.03.011. Epub 2017 Apr 12.
10
Ocular changes in familial amyloidotic polyneuropathy with dense vitreous opacities.伴有致密玻璃体混浊的家族性淀粉样多神经病的眼部改变。
Eye (Lond). 1991;5 ( Pt 1):99-105. doi: 10.1038/eye.1991.19.

引用本文的文献

1
Hereditary vitreoretinal amyloidosis with transthyretin Gly83Arg variant, a long-term study.伴有转甲状腺素蛋白Gly83Arg变异体的遗传性玻璃体视网膜淀粉样变性:一项长期研究
Eye (Lond). 2025 Feb;39(2):345-353. doi: 10.1038/s41433-024-03445-y. Epub 2024 Oct 31.
2
Contrasting presentations of the same disease: A comparison of two cases of amyloidosis presenting with eyelid involvement.同一疾病的不同表现:两例累及眼睑的淀粉样变性病例比较。
Am J Ophthalmol Case Rep. 2022 Sep 29;28:101714. doi: 10.1016/j.ajoc.2022.101714. eCollection 2022 Dec.
3
Ophthalmological manifestations of hereditary transthyretin amyloidosis.
遗传性转甲状腺素蛋白淀粉样变性的眼科表现。
Arq Bras Oftalmol. 2022 Sep-Oct;85(5):528-538. doi: 10.5935/0004-2749.20220099.
4
Ocular Involvement in Hereditary Amyloidosis.遗传性淀粉样变性的眼部表现
Genes (Basel). 2021 Jun 22;12(7):955. doi: 10.3390/genes12070955.
5
Psychopathological Dimensions in Portuguese Subjects with Transthyretin Familial Amyloid Polyneuropathy.患有转甲状腺素蛋白家族性淀粉样多神经病的葡萄牙受试者的精神病理学维度
Biomed Hub. 2017 Dec 13;2(3):1-14. doi: 10.1159/000485118. eCollection 2017 Sep-Dec.
6
Nd:YAG capsulotomy for the management of posterior capsular amyloidosis.钕钇铝石榴石激光晶状体后囊切开术治疗后囊膜淀粉样变性
Am J Ophthalmol Case Rep. 2018 Nov 10;13:50-52. doi: 10.1016/j.ajoc.2018.11.002. eCollection 2019 Mar.
7
Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study.转甲状腺素蛋白相关家族性淀粉样多神经病Val30Met患者的生命历程:一项描述性研究
J Community Genet. 2018 Jan;9(1):93-99. doi: 10.1007/s12687-017-0338-0. Epub 2017 Oct 19.
8
Bilateral optic neuropathy and intraretinal deposits after pars plana vitrectomy in amyloidosis.淀粉样变性患者行玻璃体切割术后出现双侧视神经病变及视网膜内沉积物
Indian J Ophthalmol. 2015 Jan;63(1):72-4. doi: 10.4103/0301-4738.151481.
9
Vitreous Amyloidosis as the Presenting Symptom of Familial Amyloid Polyneuropathy TTR Val30Met in a Portuguese Patient.玻璃体淀粉样变性作为葡萄牙一名携带TTR Val30Met突变的家族性淀粉样多神经病患者的首发症状
Case Rep Ophthalmol. 2014 Mar 15;5(1):92-7. doi: 10.1159/000360790. eCollection 2014 Jan.
10
Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation.在中国一个因转甲状腺素蛋白Ile107Met突变导致家族性淀粉样多神经病的家系中的多模态视网膜成像。
Eye (Lond). 2014 Apr;28(4):452-8. doi: 10.1038/eye.2014.10. Epub 2014 Jan 31.