Shahlaee Abtin, Abdelaziz Musa, Seider Michael I
Department of Ophthalmology, University of California-San Francisco, San Francisco, California, USA.
Department of Ophthalmology, The Permanente Medical Group, San Francisco, California, USA.
Ocul Oncol Pathol. 2021 Oct;7(5):326-329. doi: 10.1159/000512359. Epub 2021 Jun 2.
Trans-scleral biopsy of uveal melanoma (UM) poses an inherent risk of tumor and possibly retinal perforation. We describe a novel technique for trans-scleral biopsy of UM and evaluate its safety and efficacy in an initial cohort of patients.
A retrospective, consecutive observational case series was conducted from October 14, 2019, to April 15, 2020, at Kaiser Permanente, San Francisco, CA among patients with UM of the ciliary body or anterior choroid undergoing trans-scleral fine-needle aspiration biopsy using a novel guarded needle technique.
A total of 6 patients were included in the study, with a mean age of 64.3 (range 35-77) years (5 women 83%). Mean (±SD) tumor thickness and maximal basal diameter were 6.4 (±2.66) and 11.9 (±2.13) mm, respectively. Five out of 6 patients achieved a successful biopsy with reliable gene expression profiling (GEP) results. The only failure to obtain specimen occurred in the first attempted patient and, after a minor technique modification, all subsequent biopsies were successful. No intraoperative or short-term postoperative complications were observed in any patient.
This novel trans-scleral biopsy technique appears to be safe and effective when obtaining UM tissue for GEP. This method may provide a more controlled biopsy depth thereby minimizing the risk of tumor perforation and its associated complications while still obtaining adequate biopsy yield.
葡萄膜黑色素瘤(UM)的经巩膜活检存在肿瘤及视网膜穿孔的固有风险。我们描述了一种用于UM经巩膜活检的新技术,并在首批患者队列中评估了其安全性和有效性。
2019年10月14日至2020年4月15日,在加利福尼亚州旧金山市的凯撒医疗集团,对接受使用新型防护针技术进行经巩膜细针穿刺活检的睫状体或前脉络膜UM患者进行了一项回顾性、连续观察性病例系列研究。
共有6例患者纳入研究,平均年龄64.3岁(范围35 - 77岁)(5名女性,占83%)。平均(±标准差)肿瘤厚度和最大基底直径分别为6.4(±2.66)和11.9(±2.13)mm。6例患者中有5例活检成功,获得了可靠的基因表达谱(GEP)结果。唯一未获取到标本的情况发生在首例尝试患者中,在对技术进行 minor 修改后,随后的所有活检均成功。所有患者均未观察到术中或短期术后并发症。
这种新型经巩膜活检技术在获取用于GEP的UM组织时似乎是安全有效的。该方法可以更精确地控制活检深度,从而将肿瘤穿孔及其相关并发症的风险降至最低,同时仍能获得足够的活检标本量。