调强放疗在斯特奇-韦伯综合征弥漫性脉络膜血管瘤治疗中的应用。

IF 1.6 Q3 OPHTHALMOLOGY
Journal of Ophthalmic & Vision Research Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI:10.18502/jovr.v20.15746
Saeed Karimi, Sadra Ashrafi, Zahra Siavashpour, Mona Malekzadeh Moghani
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引用次数: 0

摘要

目的:本研究旨在报道使用调强放射治疗(IMRT)治疗弥漫性脉络膜血管瘤(DCH)的有效性和安全性。方法:对每例患者进行固定、CT模拟和靶区划定后进行IMRT计划。治疗计划的目的是将20gy的规定剂量至少递送到计划目标体积(PTV)的95%。主要的随访目标是评估IMRT作为传统3D适形放疗方法的替代方法的有效性和安全性。该病例系列涉及接受IMRT的DCH和不同程度视力损害的患者。结果:共纳入5例患者,男2例,女3例,平均年龄14.4±3.78岁。随访时间平均14.4±6.84个月。所有患者视网膜下液明显减少,肿瘤明显消退,副作用最小。imrt前手部运动视力或更好的患者视力有所改善。结论:研究结果表明,IMRT是治疗SWS患者DCH的一种有希望的低并发症治疗选择,值得进一步研究并有可能融入临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intensity-modulated Radiation Therapy in the Management of Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome.

Purpose: This study aimed to report the efficiency and safety of using intensity-modulated radiation therapy (IMRT) in treating diffuse choroidal hemangioma (DCH) in patients with Sturge-Weber syndrome (SWS).

Methods: IMRT planning was carried out for each case after patient fixation, CT simulation, and target delineation. The purpose of treatment planning was to deliver the prescribed dose of 20 Gy to at least 95% of the planning target volume (PTV). The primary follow-up goal was to evaluate the efficacy and safety of IMRT as an alternative to traditional 3D conformal radiotherapy methods. The case series involved patients with DCH and varying degrees of vision impairment who underwent IMRT.

Results: Five patients, comprising two men and three women, with an average age of 14.4 ± 3.78 years, were included in this study. These patients were followed up for an average duration of 14.4 ± 6.84 months. All patients exhibited notable reduction in subretinal fluid, significant tumor regression, and minimal side effects. Visual acuity improved in patients with pre-IMRT vision of hand motion or better.

Conclusion: The findings suggest that IMRT is a promising, low-complication treatment option for managing DCH in SWS patients, warranting further research and potential integration into clinical practice.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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