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通过30号细针穿刺活检对脉络膜黑色素瘤进行3号染色体单体性的体内荧光原位杂交。

Fluorescent in situ hybridization for monosomy 3 via 30-gauge fine-needle aspiration biopsy of choroidal melanoma in vivo.

作者信息

Young Tara A, Rao Nagesh P, Glasgow Ben J, Moral Joel N, Straatsma Bradley R

机构信息

Department of Ophthalmology, Jules Stein Eye Institute, David Geffen School of Medicine, University of California, Los Angeles, California 90095-7000, USA.

出版信息

Ophthalmology. 2007 Jan;114(1):142-6. doi: 10.1016/j.ophtha.2006.06.040. Epub 2006 Nov 9.

Abstract

OBJECTIVE

To report the feasibility of intraoperative transscleral fine-needle aspiration biopsy at plaque surgery to obtain cells for monosomy 3 analysis in patients with choroidal melanoma.

DESIGN

Consecutive interventional case series.

PARTICIPANTS

Eighteen patients (18 eyes) with choroidal melanoma who had fine-needle aspiration biopsy performed with a 30-gauge needle at time of iodine 125 plaque placement.

INTERVENTION

Cytology and cytogenetic analysis for monosomy 3 were obtained from biopsy specimens.

MAIN OUTCOME MEASURES

Cytology, cytogenetic analysis for monosomy 3, and complications and feasibility of transscleral fine-needle aspiration biopsy of choroidal melanoma in vivo.

RESULTS

Fine-needle aspiration biopsy was diagnostic of choroidal melanoma in 14 of 18 cases and resulted in viable cell cultures for fluorescent in situ hybridization (FISH) analysis in 9 cases. Fluorescent in situ hybridization for monosomy 3 was positive in 4 of the 9 cases. One patient had a mild vitreous hemorrhage. Tumors between 2 and 3 mm in height and those that yielded cells that did not attach in culture were most likely to have insufficient growth for FISH analysis.

CONCLUSIONS

Transscleral fine-needle aspiration biopsy and FISH for monosomy 3 may provide important prognostic information on patients who undergo plaque radiotherapy for choroidal melanoma.

摘要

目的

报告在脉络膜黑色素瘤患者的敷贴手术中进行术中经巩膜细针穿刺活检以获取细胞用于3号染色体单体分析的可行性。

设计

连续介入病例系列。

参与者

18例(18只眼)脉络膜黑色素瘤患者,在放置碘125敷贴时用30号针进行细针穿刺活检。

干预

从活检标本中进行细胞学检查和3号染色体单体的细胞遗传学分析。

主要观察指标

细胞学检查、3号染色体单体的细胞遗传学分析、脉络膜黑色素瘤经巩膜细针穿刺活检在体内的并发症及可行性。

结果

18例中有14例细针穿刺活检诊断为脉络膜黑色素瘤,9例获得可用于荧光原位杂交(FISH)分析的活细胞培养物。9例中有4例3号染色体单体的荧光原位杂交呈阳性。1例患者发生轻度玻璃体出血。高度在2至3毫米之间的肿瘤以及培养时细胞不贴壁的肿瘤最有可能生长不足而无法进行FISH分析。

结论

经巩膜细针穿刺活检及3号染色体单体的FISH分析可为接受敷贴放疗的脉络膜黑色素瘤患者提供重要的预后信息。

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