Suppr超能文献

正常及衰老眼中早期玻璃膜疣的形成及其与年龄相关性黄斑病变的关系:一项临床病理研究。

Early drusen formation in the normal and aging eye and their relation to age related maculopathy: a clinicopathological study.

作者信息

Sarks S H, Arnold J J, Killingsworth M C, Sarks J P

机构信息

Department of Ophthalmology, University of NSW, Sydney, Australia.

出版信息

Br J Ophthalmol. 1999 Mar;83(3):358-68. doi: 10.1136/bjo.83.3.358.

Abstract

AIM

To describe the early formation of drusen and their relation to normal aging changes at the macula and to the development of age related maculopathy (ARM).

METHOD

Histopathological features of 353 eyes without histological evidence of ARM are described and correlated with the clinical appearance. In addition, 45 of these eyes were examined by transmission electron microscopy.

RESULTS

Drusen were detected histopathologically in 177 (50%) eyes but were seen clinically in only 34% of these. Drusen were mainly small hard drusen with an occasional soft distinct drusen: no soft indistinct drusen were seen. Only those drusen deposits larger than 25-30 microns in diameter were detectable clinically. Preclinical drusen in eyes with only an occasional drusen were seen on electron microscopy as entrapment sites of coated membrane bound bodies which formed adjacent to the inner collagenous zone of Bruch's membrane. In contrast, preclinical drusen deposits in eyes with many drusen were seen as accumulations of amorphous material which appeared hyalinised by light microscopy. A distinct feature were rows of dense hyalinised microdrusen (1-2 microns in diameter), over which larger globular hyalinised drusen formed.

CONCLUSION

Histological and ultrastructural examination can recognise and distinguish the earliest drusen formed as a result of normal aging from those associated with ARM. In eyes without diffuse deposits, histologically all drusen were of the hard hyalinised variety or their derivatives; no soft drusen composed of membranous debris were found. These findings support and explain those of other authors who do not consider the presence of a few small hard drusen to be a risk factor for the development of ARM.

摘要

目的

描述玻璃膜疣的早期形成及其与黄斑正常老化变化以及年龄相关性黄斑病变(ARM)发展的关系。

方法

描述353只无ARM组织学证据的眼睛的组织病理学特征,并将其与临床表现相关联。此外,对其中45只眼睛进行了透射电子显微镜检查。

结果

组织病理学检查发现177只(50%)眼睛有玻璃膜疣,但临床仅在其中34%的眼睛中可见。玻璃膜疣主要为小的硬性玻璃膜疣,偶尔有软性清晰的玻璃膜疣:未见软性不清晰的玻璃膜疣。临床上仅能检测到直径大于25 - 30微米的玻璃膜疣沉积物。电子显微镜下,仅有偶尔几个玻璃膜疣的眼睛中的临床前期玻璃膜疣表现为包被膜结合体的截留部位,这些包被膜结合体在布鲁赫膜内胶原区附近形成。相比之下,有许多玻璃膜疣的眼睛中的临床前期玻璃膜疣沉积物表现为无定形物质的积聚,在光学显微镜下呈透明样变。一个明显的特征是有一排密集的透明样变微玻璃膜疣(直径1 - 2微米),在其上方形成较大的球状透明样变玻璃膜疣。

结论

组织学和超微结构检查能够识别并区分正常老化形成的最早玻璃膜疣与ARM相关的玻璃膜疣。在没有弥漫性沉积物的眼睛中,组织学上所有玻璃膜疣均为硬性透明样变类型或其衍生物;未发现由膜性碎片组成的软性玻璃膜疣。这些发现支持并解释了其他作者的观点,即不认为少数小的硬性玻璃膜疣的存在是ARM发生的危险因素。

相似文献

4
Macrophages related to Bruch's membrane in age-related macular degeneration.
Eye (Lond). 1990;4 ( Pt 4):613-21. doi: 10.1038/eye.1990.86.
6
Characteristics of Drusen and Bruch's membrane in postmortem eyes with age-related macular degeneration.
Arch Ophthalmol. 1997 Feb;115(2):267-73. doi: 10.1001/archopht.1997.01100150269022.
7
Basal linear deposit and large drusen are specific for early age-related maculopathy.
Arch Ophthalmol. 1999 Mar;117(3):329-39. doi: 10.1001/archopht.117.3.329.
8
Morphologic changes in age-related maculopathy.
Microsc Res Tech. 1997 Jan 15;36(2):106-22. doi: 10.1002/(SICI)1097-0029(19970115)36:2<106::AID-JEMT4>3.0.CO;2-N.

引用本文的文献

1
Retinal Vessel Changes in Geographic Atrophy in AMD: Insights From Imaging and Histology.
Invest Ophthalmol Vis Sci. 2025 Aug 1;66(11):69. doi: 10.1167/iovs.66.11.69.
2
RPE Basal Lamina Biology and Pathophysiology Related to Age-Related Macular Degeneration.
Adv Exp Med Biol. 2025;1468:15-19. doi: 10.1007/978-3-031-76550-6_3.
3
Macrophages and Age-Related Macular Degeneration.
Adv Exp Med Biol. 2025;1468:9-13. doi: 10.1007/978-3-031-76550-6_2.
5
Accelerated Brain Atrophy, Microstructural Decline and Connectopathy in Age-Related Macular Degeneration.
Biomedicines. 2024 Jan 10;12(1):147. doi: 10.3390/biomedicines12010147.
6
Multimodal Imaging of Reticular Pseudodrusen in Turkish Patients.
Turk J Ophthalmol. 2023 Oct 19;53(5):275-280. doi: 10.4274/tjo.galenos.2023.85616.
9
Small hard drusen and associated factors in early seniority.
PLoS One. 2022 Dec 22;17(12):e0279279. doi: 10.1371/journal.pone.0279279. eCollection 2022.

本文引用的文献

1
Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study.
Ophthalmology. 1995 Oct;102(10):1450-60. doi: 10.1016/s0161-6420(95)30846-9.
3
Characterization of drusen-associated glycoconjugates.
Ophthalmology. 1997 Feb;104(2):288-94. doi: 10.1016/s0161-6420(97)30322-4.
4
Characteristics of Drusen and Bruch's membrane in postmortem eyes with age-related macular degeneration.
Arch Ophthalmol. 1997 Feb;115(2):267-73. doi: 10.1001/archopht.1997.01100150269022.
5
The five-year incidence and progression of age-related maculopathy: the Beaver Dam Eye Study.
Ophthalmology. 1997 Jan;104(1):7-21. doi: 10.1016/s0161-6420(97)30368-6.
6
The prevalence of age-related maculopathy in the Rotterdam Study.
Ophthalmology. 1995 Feb;102(2):205-10. doi: 10.1016/s0161-6420(95)31034-2.
7
Age-related macular degeneration histopathologic studies. The 1992 Lorenz E. Zimmerman Lecture.
Ophthalmology. 1993 Oct;100(10):1519-35. doi: 10.1016/s0161-6420(93)31466-1.
8
Five-year incidence and disappearance of drusen and retinal pigment epithelial abnormalities. Waterman study.
Arch Ophthalmol. 1995 Mar;113(3):301-8. doi: 10.1001/archopht.1995.01100030055022.
9
Evolution of soft drusen in age-related macular degeneration.
Eye (Lond). 1994;8 ( Pt 3):269-83. doi: 10.1038/eye.1994.57.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验