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黄斑脉络膜黑色素瘤的经巩膜细针穿刺活检

Transscleral fine-needle aspiration biopsy of macular choroidal melanoma.

作者信息

Young Tara A, Burgess Barry L, Rao Nagesh P, Glasgow Ben J, Straatsma Bradley R

机构信息

Department of Ophthalmology, Jules Stein Eye Institute, 100 Stein Plaza, Los Angeles, CA 90095, USA.

出版信息

Am J Ophthalmol. 2008 Feb;145(2):297-302. doi: 10.1016/j.ajo.2007.09.028. Epub 2007 Dec 11.

Abstract

PURPOSE

To report transscleral 30-gauge fine-needle aspiration biopsy (FNAB) for cytology and cytogenetics in eyes with macular choroidal melanoma.

DESIGN

Prospective, interventional case series.

METHODS

Twenty-five patients (25 eyes) who underwent transscleral 30-gauge FNAB of macular choroidal melanoma immediately prior to iodine-125 plaque placement were included in this study, conducted at a tertiary care university hospital. The main outcome measures were FNAB feasibility, cytology, cytogenetic analysis for monosomy 3, and surgical complications.

RESULTS

Transscleral 30-gauge FNAB of choroidal melanoma in the macula was performed in 24 of 25 (96%) eyes and was not feasible owing to insufficient exposure in one eye (4%). Biopsy was diagnostic of choroidal melanoma in 17 of 24 (71%) eyes. Fluorescent in situ hybridization (FISH) and/or GeneChip 500k NspI Mapping array (Affymetrix, Santa Clara, California, USA) analysis for monosomy 3 was completed in 16 of 24 (67%) revealing monosomy 3 in five eyes and disomy 3 in 11 eyes. Retinal perforation (four eyes) did not require treatment or result in retinal detachment; submacular hemorrhage (nine eyes) and vitreous hemorrhage (five eyes) cleared spontaneously within one month.

CONCLUSION

Transscleral FNAB of macular choroidal melanoma is feasible in most eyes and frequently yields cytogenetic information relevant to prognosis.

摘要

目的

报告经巩膜30G细针穿刺活检(FNAB)用于黄斑部脉络膜黑色素瘤的细胞学和细胞遗传学检查。

设计

前瞻性、介入性病例系列研究。

方法

本研究在一家三级医疗大学医院进行,纳入25例患者(25只眼),这些患者在接受碘-125敷贴治疗前即刻对黄斑部脉络膜黑色素瘤进行了经巩膜30G FNAB。主要观察指标为FNAB的可行性、细胞学、3号染色体单体性的细胞遗传学分析及手术并发症。

结果

25只眼中24只(96%)成功进行了黄斑部脉络膜黑色素瘤的经巩膜30G FNAB,1只眼(4%)因暴露不足未成功。24只眼中17只(71%)活检诊断为脉络膜黑色素瘤。24只眼中16只(67%)完成了3号染色体单体性的荧光原位杂交(FISH)和/或基因芯片500k NspI图谱阵列(美国加利福尼亚州圣克拉拉市Affymetrix公司)分析,其中5只眼显示3号染色体单体性,11只眼显示3号染色体二体性。视网膜穿孔(4只眼)无需治疗,也未导致视网膜脱离;黄斑下出血(9只眼)和玻璃体积血(5只眼)在1个月内自行吸收。

结论

黄斑部脉络膜黑色素瘤的经巩膜FNAB在大多数眼中是可行的,且常能获得与预后相关的细胞遗传学信息。

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