Surgical management and visual outcomes of optic-pathway cavernous malformations: A comprehensive literature review of 80 reported cases (1979 – 2025)

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
Shrey Kumar Shah , Asmita Indurkar , Biren Khimji Patel
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Abstract

Objective

Cavernous malformations (CMs) of the optic chiasm, optic tract, and hypothalamus are exceedingly rare. Most patients present with acute or progressive visual loss, and surgery aims to maximize visual recovery while minimizing neural manipulation. We describe an updated review of all reported operated optic-pathway cavernomas to clarify surgical strategies and visual outcomes.

Methodology

PubMed, MEDLINE, and Google Scholar were searched with the terms optic pathway cavernoma, optic chiasm cavernoma, hypothalamic cavernoma, and surgical outcomes. Eighty published cases (1979 – May 2025) were analyzed for presentation, surgical corridor, extent of resection, and postoperative vision.

Results

Among 80 patients (42 females, 36 males; mean age 34.9 ± 11.7 years), visual disturbance was the initial symptom in 75/78 with available data (96.2 %); headache occurred in 29 (37 %). Surgical corridors included fronto-temporal/pterional (55 %), mid-line subfrontal or inter-hemispheric (16 %), orbito-zygomatic (6 %), EEA/TNTS (6 %), and other or unspecified craniotomies (16 %). Gross-total resection (GTR) was achieved in 59 patients (73.8 %). Post-operative vision (reported in 75 patients) improved in 54 (72.0 %), stabilised in 17 (22.7 %), and deteriorated in 4 (5.3 %). GTR conferred the highest likelihood of improvement (78.9 % vs 50 % after subtotal resection). The EEA/TNTS corridor, now reported in six cases, allowed complete excision without brain retraction or Sylvian fissure dissection and achieved visual improvement or stability in all patients.

Conclusion

Early surgical excision offers visual improvement or preservation in more than 94 % of optic-pathway CM cases, with GTR the strongest predictor of favourable outcome. The endoscopic endonasal route, when guided by neuronavigation and multilayer skull-base reconstruction, provides direct mid-line access with minimal manipulation of critical perforators and should be considered a first-line corridor for mid-line chiasmatic or retro-chiasmatic lesions.
1979 - 2025年80例海绵状血管瘤的外科治疗与视力:综合文献回顾
目的视神经交叉、视神经束和下丘脑的海绵状畸形极为罕见。大多数患者表现为急性或进行性视力丧失,手术旨在最大限度地恢复视力,同时尽量减少神经操作。我们描述了所有报道的手术光通路海绵瘤的最新回顾,以澄清手术策略和视力结果。方法检索pubmed、MEDLINE和谷歌Scholar,检索词为视神经通路海绵状瘤、视交叉海绵状瘤、下丘脑海绵状瘤和手术结果。我们分析了80例已发表的病例(1979 - 2025年5月)的表现、手术通道、切除程度和术后视力。结果80例患者中,女性42例,男性36例;平均年龄34.9 ± 11.7岁),有资料的78例中有75例以视力障碍为首发症状(96.2 %);29例(37% %)出现头痛。手术通道包括额颞/翼位(55% %)、额下中线或半球间(16% %)、眶颧(6 %)、EEA/TNTS(6 %)和其他或未指定的开颅手术(16 %)。59例患者(73.8% %)实现了总切除(GTR)。术后视力(75例)改善54例(72.0 %),稳定17例(22.7 %),恶化4例(5.3 %)。GTR具有最高的改善可能性(78.9% % vs 50. %次全切除)。EEA/TNTS通道,目前报道了6例,允许完全切除,无脑回缩或Sylvian裂夹层,并在所有患者中获得视力改善或稳定性。结论早期手术切除可改善或保留94% %以上的视通路CM病例的视力,GTR是预后良好的最强预测因子。在神经导航和多层颅底重建的指导下,内窥镜鼻内路径提供了直接的中线通道,对关键穿支的操作最少,应被视为中线交叉或后交叉病变的一线通道。
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来源期刊
Clinical Neurology and Neurosurgery
Clinical Neurology and Neurosurgery 医学-临床神经学
CiteScore
3.70
自引率
5.30%
发文量
358
审稿时长
46 days
期刊介绍: Clinical Neurology and Neurosurgery is devoted to publishing papers and reports on the clinical aspects of neurology and neurosurgery. It is an international forum for papers of high scientific standard that are of interest to Neurologists and Neurosurgeons world-wide.
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