Evidence map›Paper›PMID 42519777›Full record

ArticleFrontiers in medicine2026

Case report: Two cases of juxtapapillary retinal capillary hemangioma treated with intraocular cryotherapy.

Weiwei Zhang, Yiliu Yang, Chengda Ren, Xiaoshuang Jiang, Fang Lu

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Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Weiwei ZhangDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Yiliu YangDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Chengda RenDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Xiaoshuang JiangDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Fang LuDepartment of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Juxtapapillary retinal capillary hemangioma (JRCH) is a rare vascular tumor arising from or adjacent to the optic disc and may cause visual impairment due to exudation and vitreoretinal interface complications. Its management remains challenging because of the risk of optic nerve damage and the lack of standardized treatment protocols. Cryotherapy is commonly applied transsclerally for peripheral retinal capillary hemangioma (RCH) but has been rarely used for JRCH. Reports of intraocular cryotherapy are even more limited. Case presentation: We report two pediatric cases of isolated JRCH with an endophytic growth pattern. The first case involved a 6-year-old girl presenting with JRCH complicated by exudative retinal detachment. She showed a limited response to repeated laser photocoagulation and intravitreal anti-vascular endothelial growth factor (anti-VEGF) therapy, and underwent pars plana vitrectomy (PPV) to relieve vitreoretinal traction. However, peripapillary vascular dilation and exudation persisted. She subsequently underwent intraocular cryotherapy, resulting in tumor regression and reduced exudation, with stable disease maintained during follow-up. The second case involved a 10-year-old girl presenting with JRCH complicated by macular edema and significant vitreoretinal traction. She underwent PPV, epiretinal membrane peeling, and intraocular cryotherapy. The tumor demonstrated a similarly favorable response to intraocular cryotherapy. Conclusion: Anatomical stabilization was observed during the available follow-up period after treatment including intraocular cryotherapy. These cases provide preliminary clinical experience with intraocular cryotherapy for the management of complex JRCH. Further studies are needed to evaluate its safety, efficacy, and long-term outcomes.

Indexed as

case reportintraocular cryotherapyjuxtapapillary retinal capillary hemangiomamultimodal imagingpars plana vitrectomy

Identifiers

PMID42519777
PMCPMC13382540

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