Uveal melanoma: the value of molecular genetic testing for early detection of metastatic disease. Clinical case

V. Yarovaya, А. V. Golanov, V. V. Nazarova, А. R. Zaretskii, I. A. Levashov, А. К. Kulagina, Т. V. Melnikova, А. D. Matyaeva, А. Yarovoy
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引用次数: 0

Abstract

To date, the issue of not only timely diagnosis and treatment of patients with uveal melanoma (UM), but also the prediction of this pathology remains relevant. The technology of fine needle aspiration biopsy (FNAB) makes it possible to assess the risk of developing metastatic disease using tumor specimen in patients undergoing organ-preserving treatment by cytological and molecular genetic testing in the primary intraocular lesion. Here we present a case of newly identified locally advanced (T3a) UM, outline the possibilities of organ-preserving treatment using Gamma Knife stereotactic radiosurgery, and also demonstrate the feasibility of conducting a comprehensive prognostic testing on FNAB material, including cytological and molecular genetic and morphological prognostic factors. The results of this testing have made it possible to recommend a more frequent surveillance monitoring regime for metastatic disease, which ultimately led to the early detection of UM liver metastases, followed by their successful treatment.
葡萄膜黑色素瘤:分子基因检测对早期发现转移性疾病的价值。临床病例
迄今为止,不仅要及时诊断和治疗葡萄膜黑色素瘤(UM)患者,还要对这种病理变化进行预测,这个问题仍然十分重要。细针穿刺活检(FNAB)技术可通过对眼内原发病灶进行细胞学和分子遗传学检测,评估接受器官保留治疗的患者肿瘤标本发生转移性疾病的风险。在此,我们介绍了一例新发现的局部晚期(T3a)UM,概述了使用伽玛刀立体定向放射外科手术进行保留器官治疗的可能性,同时还展示了对 FNAB 材料进行全面预后检测的可行性,包括细胞学和分子遗传学及形态学预后因素。这项检测的结果使我们有可能建议对转移性疾病进行更频繁的监测,从而最终及早发现 UM 肝转移灶,并对其进行成功治疗。
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