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伴有弥漫性玻璃体播散的非典型视网膜细胞瘤:一项深入研究

Atypical retinocytoma with diffuse vitreous seeds: An insight.

作者信息

Shah Parag K, Narendran V, Manayath George J, Chowdhary Somya

机构信息

Department of Pediatric Retina and Ocular Oncology, Aravind Eye Hospital, Coimbatore, India.

出版信息

Oman J Ophthalmol. 2011 May;4(2):81-3. doi: 10.4103/0974-620X.83659.

DOI:10.4103/0974-620X.83659
PMID:21897624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3160075/
Abstract

Retinocytoma is a rare benign form of retinoblastoma. It is usually found on routine examinations and also while screening families of patients with retinoblastoma. Distinctive features are a translucent retinal mass with calcification, retinal pigment epithelial disturbance, chorioretinal atrophy and absence of growth. We report a case with all the above features along with diffuse vitreous seeds and optical coherence tomographic documentation of intralesional cavitary lesions.

摘要

视网膜细胞瘤是视网膜母细胞瘤的一种罕见良性形式。它通常在常规检查中被发现,也在对视网膜母细胞瘤患者的家族进行筛查时被发现。其特征为伴有钙化的半透明视网膜肿块、视网膜色素上皮紊乱、脉络膜视网膜萎缩且无生长现象。我们报告了一例具有上述所有特征的病例,同时伴有弥漫性玻璃体播散以及病灶内空洞性病变的光学相干断层扫描记录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/b38e2c87fc1f/OJO-4-81-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/46e13fe9b0f4/OJO-4-81-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/a8a3aae96c08/OJO-4-81-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/144edc24f0e4/OJO-4-81-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/b38e2c87fc1f/OJO-4-81-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/46e13fe9b0f4/OJO-4-81-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/a8a3aae96c08/OJO-4-81-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/144edc24f0e4/OJO-4-81-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470a/3160075/b38e2c87fc1f/OJO-4-81-g004.jpg

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Retinocytoma: understanding pathogenesis, diagnosis, and treatment approaches.视网膜细胞瘤:了解发病机制、诊断及治疗方法。
Int J Retina Vitreous. 2025 Feb 25;11(1):20. doi: 10.1186/s40942-025-00642-z.
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Multifocal Retinocytoma Associated With Intronic Acceptor Splice Site Variants in the RB1 Gene.与RB1基因内含子受体剪接位点变异相关的多灶性视网膜细胞瘤

本文引用的文献

1
Observations on 17 patients with retinocytoma.17例视网膜细胞瘤患者的观察结果。
Arch Ophthalmol. 2000 Feb;118(2):199-205. doi: 10.1001/archopht.118.2.199.
2
Retinoma associated with vitreous seeding.伴有玻璃体播散的视网膜瘤。
Am J Ophthalmol. 1995 Apr;119(4):522-3. doi: 10.1016/s0002-9394(14)71246-2.
3
Significance of retinoma and phthisis bulbi for retinoblastoma.视网膜瘤和眼球痨对视网膜母细胞瘤的意义。
Cureus. 2024 Oct 3;16(10):e70786. doi: 10.7759/cureus.70786. eCollection 2024 Oct.
Ophthalmology. 1982 Dec;89(12):1393-9. doi: 10.1016/s0161-6420(82)34622-9.
4
Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?视网膜瘤:视网膜母细胞瘤的自发消退还是突变的良性表现?
Br J Cancer. 1982 Apr;45(4):513-21. doi: 10.1038/bjc.1982.87.
5
Spontaneous regression of bilateral multifocal retinoblastoma with preservation of normal visual acuity.双侧多灶性视网膜母细胞瘤自发消退并保留正常视力。
Ann Ophthalmol. 1974 Nov;6(11):1192-4.