先天性視網膜動靜脈畸形1例_Chinese Journal of Ocular Fundus Diseases

Authors：

徐愛珍 ¹ ,  李傳寶 ² , 劉德國 ³ , 宋國紅 ⁴ , 周亞蘭 ²

1. ;
2. ;
3. ;
4. ;

Corresponding?author：

李傳寶, Email: 13853708298@126.com

Keywords：

視網膜動靜脈畸形; 眼動靜脈畸形; 病例報告

DOI：

10.3760/cma.j.cn511434-20251013-00443

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Citation： 徐愛珍, 李傳寶, 劉德國, 宋國紅, 周亞蘭. 先天性視網膜動靜脈畸形1例. Chinese Journal of Ocular Fundus Diseases, 2026, 42(4): 347-349. doi: 10.3760/cma.j.cn511434-20251013-00443 Copy

1.	Meyer CH, Rodrigues EB, Mennel S, et al. Functional and anatomical investigations in racemose haemangioma[J]. Acta Ophthalmol Scand, 2007, 85(7): 764-771. DOI: 10.1111/j.1600-0420.2007.00911.x.
2.	張軼, 張美霞, 陳大年, 等. 建議將“視網膜蔓狀血管瘤”更名為“先天性視網膜動靜脈畸形”[J]. 中華眼底病雜志, 2014, 30(5): 516-517. DOI: 10.3760/cma.j.issn.1005-1015.2014.05.022.Zhang Y, Zhang MX, Chen DN, et al. Suggesting renaming “retinal racemose hemangioma” to “congenital retinal arteriovenous malformation”[J]. Chin J Ocul Fundus Dis, 2014, 30(5): 516-517. DOI: 10.3760/cma.j.issn.1005-1015.2014.05.022.
3.	張秋雁, 趙長影, 于偉濤, 等. 視網膜蔓狀血管瘤一例[J]. 中華眼底病雜志, 2010, 26(5): 488-489. DOI: 10.3760/cma.j.issn.10051015.2010.05.29.Zhang QY, Zhao CY, Yu WT, et al. A case of retinal tufted angioma[J]. Chin J Ocul Fundus Dis, 2010, 26(5): 488-489. DOI: 10.3760/cma.j.issn.10051015.2010.05.29.
4.	Hupin N, Cahill T, Boschi A, et al. Macular edema in Wyburn-Mason syndrome: resolution with anti-VEGF intravitreal injections. Case report and review of the literature[J/OL]. Am J Ophthalmol Case Rep, 2024, 36: 102209[2024-10-30]. https://pubmed.ncbi.nlm.nih.gov/39669759/. DOI: 10.1016/j.ajoc.2024.102209.
5.	Vaithialingam B, Gopal S, Sohrab M. Catheter embolization of an orbital arteriovenous fistula in a patient with Wyburn-Mason syndrome[J/OL]. Cureus, 2023, 15(3): e36949[2023-03-31]. https://pubmed.ncbi.nlm.nih.gov/37131550/. DOI: 10.7759/cureus.36949.
6.	Ahmad Tarmizi NN, Bastion MC, Abdul Aziz RA, et al. Retinal racemose hemangioma with optic neuropathy in a child[J/OL]. Cureus, 2021, 13(8): e17620[2021-08-31]. https://pubmed.ncbi.nlm.nih.gov/34646671/. DOI: 10.7759/cureus.17620.
7.	Archer DB, Deutman A, Ernest JT, et al. Arteriovenous communications of the retina[J]. Am J Ophthalmol, 1973, 75(2): 224-241. DOI: 10.1016/0002-9394(73)91018-0.
8.	Qin XJ, Huang C, Lai K. Retinal vein occlusion in retinal racemose hemangioma: a case report and literature review of ocular complications in this rare retinal vascular disorder[J/OL]. BMC Ophthalmol, 2014, 14: 101[2014-08-21]. https://pubmed.ncbi.nlm.nih.gov/25142779/. DOI: 10.1186/1471-2415-14-101.
9.	楊晨, 劉瑜玲, 竇宏亮, 等. 視網膜蔓狀血管瘤合并半側性視網膜靜脈阻塞一例[J]. 中華眼底病雜志, 2011, 27(2): 189-190. DOI: 10.3760/cma.j.issn.1005-1015.2011.02.027.Yang C, Liu YL, Dou HL, et al. A case of retinal tufted angioma combined with hemiplegic retinal vein occlusion[J]. Chin J Ocul Fundus Dis, 2011, 27(2): 189-190. DOI: 10.3760/cma.j.issn.1005-1015.2011.02.027.
10.	侯澤江, 江兆源. 視網膜蔓狀血管瘤并發視網膜分支靜脈阻塞一例[J]. 中華眼科雜志, 2012, 48(9): 851-852. DOI: 10.3760/cma.j.issn.0412-4081.2012.09.020.Hou ZJ, Jiang ZY. A case of retinal tufted angioma complicated with retinal branch vein occlusion[J]. Chin J Ophthalmol, 2012, 48(9): 851-852. DOI: 10.3760/cma.j.issn.0412-4081.2012.09.020.
11.	Papageorgiou KI, Ghazi-Nouri SM, Andreou PS. Vitreous and subretinal haemorrhage: an unusual complication of retinal racemose haemangioma[J]. Clin Exp Ophthalmol, 2006, 34(2): 176-177. DOI: 10.1111/j.1442-9071.2006.01178.x.
12.	Vishal R, Avadesh O, Srinivas R, et al. Retinal racemose hemangioma with retinal artery macroaneurysm: optical coherence tomography angiography (OCTA) findings[J]. Am J Ophthalmol Case Rep, 2018, 11: 98-100. DOI: 10.1016/j.ajoc.2018.06.018.
13.	柴麗娜, 雷春燕, 高昇, 等. 孤立先天性視網膜動靜脈畸形合并玻璃體出血和內界膜下出血1例并文獻復習[J]. 山東大學耳鼻喉眼學報, 2023, 37(2): 67-70. DOI: 10.6040/j.issn.1673-3770.0.2021.521.Chai LN, Lei CY, Gao S, et al. Isolated congenital retinal arteriovenous malformation with vitreous hemorrhage and sub-inner limiting membrane hemorrhage: a case report and literature review[J]. J Otolaryngol Ophthalmol Shandong University, 2023, 37(2): 67-70. DOI: 10.6040/j.issn.1673-3770.0.2021.521.
14.	Xu Y, Luo L, Yang B, et al. Five-year follow-up of a spontaneously progressive retinal racemose hemangioma[J]. Retin Cases Brief Rep, 2024, 18(2): 199-201. DOI: 10.1097/ICB.0000000000001370.
15.	Akiyama Y, Muraoka Y, Kogo T, et al. Multimodal chorioretinal imaging in Wyburn-Mason syndrome: a case report[J/OL]. Heliyon, 2024, 10(14): e34872[2024-07-20]. https://pubmed.ncbi.nlm.nih.gov/39149014/. DOI: 10.1016/j.heliyon.2024.e34872.
16.	Yamao S, Kusaka S. Wyburn-Mason syndrome in an 11-year-old girl[J/OL]. JAMA Ophthalmol, 2020, 138(5): e191452[2020-05-01]. https://pubmed.ncbi.nlm.nih.gov/32407445/. DOI: 10.1001/jamaophthalmol.2019.1452.
17.	Kolomeyer AM, Laviolette R, Winter TW. Wyburn-Mason syndrome[J/OL]. Ophthalmology, 2016, 123(1): 50[2016-01-01]. https://pubmed.ncbi.nlm.nih.gov/26707436/. DOI: 10.1016/j.ophtha.2015.10.033.
18.	覃冬, 楊俊峰, 廖志強, 等. 兒童Wyburn-Mason綜合征一例[J]. 中華實驗眼科雜志, 2016, 34(7): 606-607. DOI: 10.3760/cma.j.issn.2095-0160.2016.07.007.Qin D, Yang JF, Liao ZQ, et al. A case of Wyburn-Mason syndrome in children[J]. Chin J Exp Ophthalmol, 2016, 34(7): 606-607. DOI: 10.3760/cma.j.issn.2095-0160.2016.07.007.
19.	于攀, 許賀. 先天性視網膜動靜脈畸形[J]. 中華眼底病雜志, 2024, 40(2): 2. DOI: 10.3760/cma.j.cn511434-20221017-00548.Yu P, Xu H. Congenital retinal arteriovenous malformations[J]. Chin J Ocul Fundus Dis, 2024, 40(2): 2. DOI: 10.3760/cma.j.cn511434-20221017-00548.
20.	王宏超, 馬利平. Sturge-Weber綜合征3例報告并文獻復習[J]. 中國臨床醫學影像雜志, 2019, 30(5): 368-370. DOI: 10.12117/jccmi.2019.05.017.Wang HC, Ma LP. Sturge-Weber syndrome: report of three cases and review of literature[J]. J Chin Clin Med Imaging, 2019, 30(5): 368-370. DOI: 10.12117/jccmi.2019.05.017.
21.	Shameem Y, Irshad S, Mirza N, et al. Wyburn-Mason syndrome: a narrative review[J/OL]. Cureus, 2024, 16(8): e68070[2024-08-28]. https://pubmed.ncbi.nlm.nih.gov/39347253/. DOI: 10.7759/cureus.68070.

1. Meyer CH, Rodrigues EB, Mennel S, et al. Functional and anatomical investigations in racemose haemangioma[J]. Acta Ophthalmol Scand, 2007, 85(7): 764-771. DOI: 10.1111/j.1600-0420.2007.00911.x.
2. 張軼, 張美霞, 陳大年, 等. 建議將“視網膜蔓狀血管瘤”更名為“先天性視網膜動靜脈畸形”[J]. 中華眼底病雜志, 2014, 30(5): 516-517. DOI: 10.3760/cma.j.issn.1005-1015.2014.05.022.Zhang Y, Zhang MX, Chen DN, et al. Suggesting renaming “retinal racemose hemangioma” to “congenital retinal arteriovenous malformation”[J]. Chin J Ocul Fundus Dis, 2014, 30(5): 516-517. DOI: 10.3760/cma.j.issn.1005-1015.2014.05.022.
3. 張秋雁, 趙長影, 于偉濤, 等. 視網膜蔓狀血管瘤一例[J]. 中華眼底病雜志, 2010, 26(5): 488-489. DOI: 10.3760/cma.j.issn.10051015.2010.05.29.Zhang QY, Zhao CY, Yu WT, et al. A case of retinal tufted angioma[J]. Chin J Ocul Fundus Dis, 2010, 26(5): 488-489. DOI: 10.3760/cma.j.issn.10051015.2010.05.29.
4. Hupin N, Cahill T, Boschi A, et al. Macular edema in Wyburn-Mason syndrome: resolution with anti-VEGF intravitreal injections. Case report and review of the literature[J/OL]. Am J Ophthalmol Case Rep, 2024, 36: 102209[2024-10-30]. https://pubmed.ncbi.nlm.nih.gov/39669759/. DOI: 10.1016/j.ajoc.2024.102209.
5. Vaithialingam B, Gopal S, Sohrab M. Catheter embolization of an orbital arteriovenous fistula in a patient with Wyburn-Mason syndrome[J/OL]. Cureus, 2023, 15(3): e36949[2023-03-31]. https://pubmed.ncbi.nlm.nih.gov/37131550/. DOI: 10.7759/cureus.36949.
6. Ahmad Tarmizi NN, Bastion MC, Abdul Aziz RA, et al. Retinal racemose hemangioma with optic neuropathy in a child[J/OL]. Cureus, 2021, 13(8): e17620[2021-08-31]. https://pubmed.ncbi.nlm.nih.gov/34646671/. DOI: 10.7759/cureus.17620.
7. Archer DB, Deutman A, Ernest JT, et al. Arteriovenous communications of the retina[J]. Am J Ophthalmol, 1973, 75(2): 224-241. DOI: 10.1016/0002-9394(73)91018-0.
8. Qin XJ, Huang C, Lai K. Retinal vein occlusion in retinal racemose hemangioma: a case report and literature review of ocular complications in this rare retinal vascular disorder[J/OL]. BMC Ophthalmol, 2014, 14: 101[2014-08-21]. https://pubmed.ncbi.nlm.nih.gov/25142779/. DOI: 10.1186/1471-2415-14-101.
9. 楊晨, 劉瑜玲, 竇宏亮, 等. 視網膜蔓狀血管瘤合并半側性視網膜靜脈阻塞一例[J]. 中華眼底病雜志, 2011, 27(2): 189-190. DOI: 10.3760/cma.j.issn.1005-1015.2011.02.027.Yang C, Liu YL, Dou HL, et al. A case of retinal tufted angioma combined with hemiplegic retinal vein occlusion[J]. Chin J Ocul Fundus Dis, 2011, 27(2): 189-190. DOI: 10.3760/cma.j.issn.1005-1015.2011.02.027.
10. 侯澤江, 江兆源. 視網膜蔓狀血管瘤并發視網膜分支靜脈阻塞一例[J]. 中華眼科雜志, 2012, 48(9): 851-852. DOI: 10.3760/cma.j.issn.0412-4081.2012.09.020.Hou ZJ, Jiang ZY. A case of retinal tufted angioma complicated with retinal branch vein occlusion[J]. Chin J Ophthalmol, 2012, 48(9): 851-852. DOI: 10.3760/cma.j.issn.0412-4081.2012.09.020.
11. Papageorgiou KI, Ghazi-Nouri SM, Andreou PS. Vitreous and subretinal haemorrhage: an unusual complication of retinal racemose haemangioma[J]. Clin Exp Ophthalmol, 2006, 34(2): 176-177. DOI: 10.1111/j.1442-9071.2006.01178.x.
12. Vishal R, Avadesh O, Srinivas R, et al. Retinal racemose hemangioma with retinal artery macroaneurysm: optical coherence tomography angiography (OCTA) findings[J]. Am J Ophthalmol Case Rep, 2018, 11: 98-100. DOI: 10.1016/j.ajoc.2018.06.018.
13. 柴麗娜, 雷春燕, 高昇, 等. 孤立先天性視網膜動靜脈畸形合并玻璃體出血和內界膜下出血1例并文獻復習[J]. 山東大學耳鼻喉眼學報, 2023, 37(2): 67-70. DOI: 10.6040/j.issn.1673-3770.0.2021.521.Chai LN, Lei CY, Gao S, et al. Isolated congenital retinal arteriovenous malformation with vitreous hemorrhage and sub-inner limiting membrane hemorrhage: a case report and literature review[J]. J Otolaryngol Ophthalmol Shandong University, 2023, 37(2): 67-70. DOI: 10.6040/j.issn.1673-3770.0.2021.521.
14. Xu Y, Luo L, Yang B, et al. Five-year follow-up of a spontaneously progressive retinal racemose hemangioma[J]. Retin Cases Brief Rep, 2024, 18(2): 199-201. DOI: 10.1097/ICB.0000000000001370.
15. Akiyama Y, Muraoka Y, Kogo T, et al. Multimodal chorioretinal imaging in Wyburn-Mason syndrome: a case report[J/OL]. Heliyon, 2024, 10(14): e34872[2024-07-20]. https://pubmed.ncbi.nlm.nih.gov/39149014/. DOI: 10.1016/j.heliyon.2024.e34872.
16. Yamao S, Kusaka S. Wyburn-Mason syndrome in an 11-year-old girl[J/OL]. JAMA Ophthalmol, 2020, 138(5): e191452[2020-05-01]. https://pubmed.ncbi.nlm.nih.gov/32407445/. DOI: 10.1001/jamaophthalmol.2019.1452.
17. Kolomeyer AM, Laviolette R, Winter TW. Wyburn-Mason syndrome[J/OL]. Ophthalmology, 2016, 123(1): 50[2016-01-01]. https://pubmed.ncbi.nlm.nih.gov/26707436/. DOI: 10.1016/j.ophtha.2015.10.033.
18. 覃冬, 楊俊峰, 廖志強, 等. 兒童Wyburn-Mason綜合征一例[J]. 中華實驗眼科雜志, 2016, 34(7): 606-607. DOI: 10.3760/cma.j.issn.2095-0160.2016.07.007.Qin D, Yang JF, Liao ZQ, et al. A case of Wyburn-Mason syndrome in children[J]. Chin J Exp Ophthalmol, 2016, 34(7): 606-607. DOI: 10.3760/cma.j.issn.2095-0160.2016.07.007.
19. 于攀, 許賀. 先天性視網膜動靜脈畸形[J]. 中華眼底病雜志, 2024, 40(2): 2. DOI: 10.3760/cma.j.cn511434-20221017-00548.Yu P, Xu H. Congenital retinal arteriovenous malformations[J]. Chin J Ocul Fundus Dis, 2024, 40(2): 2. DOI: 10.3760/cma.j.cn511434-20221017-00548.
20. 王宏超, 馬利平. Sturge-Weber綜合征3例報告并文獻復習[J]. 中國臨床醫學影像雜志, 2019, 30(5): 368-370. DOI: 10.12117/jccmi.2019.05.017.Wang HC, Ma LP. Sturge-Weber syndrome: report of three cases and review of literature[J]. J Chin Clin Med Imaging, 2019, 30(5): 368-370. DOI: 10.12117/jccmi.2019.05.017.
21. Shameem Y, Irshad S, Mirza N, et al. Wyburn-Mason syndrome: a narrative review[J/OL]. Cureus, 2024, 16(8): e68070[2024-08-28]. https://pubmed.ncbi.nlm.nih.gov/39347253/. DOI: 10.7759/cureus.68070.

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先天性視網膜動靜脈畸形1例

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