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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.

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/b9441ef38756/brjopthal00195-0063-a.jpg

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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.

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