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婴儿囊性黄斑病变

Infantile cystoid maculopathy.

作者信息

Trese M T, Foos R Y

出版信息

Br J Ophthalmol. 1980 Mar;64(3):206-10. doi: 10.1136/bjo.64.3.206.

DOI:10.1136/bjo.64.3.206
PMID:7387953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1039388/
Abstract

Three premature infants with no family history of eye disease showed bilateral cystoid maculopathy on post-mortem examination. These macular lesions are indistinguishable macroscopically from the macular lesions of sex-linked juvenile retinoschisis. Cystoid change was observed at various vertical retinal levels. The oldest child had a schisis cavity within the nerve fibre layer. All cases had reduced numbers of retinal ganglion cells and central nervous system (CNS) abnormalities. The authors believe these are the first reported cases of a cystoid macular lesion present at birth and the first description of the pathological features of a cystoid macular lesion in infants.

摘要

三名无眼部疾病家族史的早产儿在尸检时显示双侧黄斑囊样病变。这些黄斑病变在肉眼上与性连锁青少年视网膜劈裂症的黄斑病变无法区分。在视网膜不同垂直层面均观察到囊样改变。年龄最大的患儿在神经纤维层内有一个劈裂腔。所有病例的视网膜神经节细胞数量均减少,且存在中枢神经系统(CNS)异常。作者认为这些是首次报道的出生时即存在的黄斑囊样病变病例,也是对婴儿黄斑囊样病变病理特征的首次描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/c76fa4853864/brjopthal00195-0065-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/b9441ef38756/brjopthal00195-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/b04cd9587bf3/brjopthal00195-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/4c1c0c4e8182/brjopthal00195-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/6281d448b579/brjopthal00195-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/c76fa4853864/brjopthal00195-0065-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/b9441ef38756/brjopthal00195-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/b04cd9587bf3/brjopthal00195-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/4c1c0c4e8182/brjopthal00195-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/6281d448b579/brjopthal00195-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/575c/1039388/c76fa4853864/brjopthal00195-0065-a.jpg

相似文献

1
Infantile cystoid maculopathy.婴儿囊性黄斑病变
Br J Ophthalmol. 1980 Mar;64(3):206-10. doi: 10.1136/bjo.64.3.206.
2
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3
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[Optical coherence tomography in optic pit and associated maculopathy].[光学相干断层扫描在视盘小凹及相关黄斑病变中的应用]
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Congenital retinoschisis.先天性视网膜劈裂症
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Congenital retinoschisis.先天性视网膜劈裂症
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引用本文的文献

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Severity of cystoid macular oedema in preterm infants observed using hand-held spectral domain optical coherence tomography improves weekly with postmenstrual age.早产儿使用手持谱域光相干断层扫描观察到的囊样黄斑水肿严重程度随胎龄增加而每周改善。
Eye (Lond). 2023 Oct;37(14):3009-3014. doi: 10.1038/s41433-023-02461-8. Epub 2023 Mar 16.
2
Insights into the developing fovea revealed by imaging.成像技术揭示的黄斑发育奥秘。
Prog Retin Eye Res. 2022 Sep;90:101067. doi: 10.1016/j.preteyeres.2022.101067. Epub 2022 May 17.
3
Dynamics of human foveal development after premature birth.

本文引用的文献

1
Histopathology of juvenile retinoschisis.青少年视网膜劈裂症的组织病理学
Arch Ophthalmol. 1968 Jan;79(1):49-53. doi: 10.1001/archopht.1968.03850040051014.
2
Juvenile sex-linked retinoschisis.
Bibl Ophthalmol. 1969;79:363-70.
3
Pathology of hereditary juvenile retinoschisis.遗传性青少年视网膜劈裂症的病理学
Arch Ophthalmol. 1972 Aug;88(2):131-8. doi: 10.1001/archopht.1972.01000030133002.
早产儿人类黄斑发育的动力学。
Ophthalmology. 2011 Dec;118(12):2315-25. doi: 10.1016/j.ophtha.2011.05.028. Epub 2011 Sep 21.
4
The incidence, pathogenesis and treatment of cystoid macular edema following cataract surgery.白内障手术后黄斑囊样水肿的发病率、发病机制及治疗
Trans Am Ophthalmol Soc. 1998;96:557-634.
4
The effect of intrauterine surgical procedures on the development of the primate eye.宫内手术操作对灵长类动物眼睛发育的影响。
Invest Ophthalmol. 1969 Feb;8(1):51-60.
5
A system for the macroexamination of eyes in the laboratory.一种用于实验室眼部宏观检查的系统。
Am J Clin Pathol. 1973 May;59(5):674-83. doi: 10.1093/ajcp/59.5.674.