Ultrasonographic and histopathological correlation in choroidal melanoma: survival outcomes from a single-center study in Serbia.

IF 1.8 4区 医学 Q3 DERMATOLOGY
Melanoma Research Pub Date : 2026-06-01 Epub Date: 2026-03-02 DOI:10.1097/CMR.0000000000001092
Dolika D Vasović, Dejan M Rašić, Bojana Dačić-Krnjaja, Tanja Kalezić, Jovana Kuzmanović Pfićer, Jelena Simonović, Jelena Vasilijević, Igor Kovačević, Sanja Petrović-Pajić, Ivan Marjanović
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引用次数: 0

Abstract

To compare ultrasonographic and histopathological measurements of tumor size in enucleated eyes with choroidal melanoma and to evaluate the prognostic significance of tumor dimensions and morphological characteristics in a Serbian cohort. This retrospective study included 59 consecutive patients with histopathologically confirmed choroidal melanoma who underwent enucleation at the University Eye Hospital, Clinical Centre of Serbia. All ultrasonographic examinations, surgical procedures, and histopathological assessments were performed by single dedicated subspecialists. Preoperative B-scan ultrasonography was used to measure tumor base diameter and thickness, which were compared with postoperative macroscopic histopathological dimensions using paired statistical tests, Bland-Altman analysis, and intraclass correlation coefficients (ICC). Survival outcomes were assessed using Pearson and Spearman correlations and Kaplan-Meier analysis. Patients were followed for a minimum of 1 year, with some monitored for up to 5 years. Data are presented as mean ± SD. The mean ultrasonographic base diameter and thickness were 14.63 ± 3.98 and 10.34 ± 3.54 mm, respectively, compared with 18.04 ± 6.54 and 10.55 ± 3.72 mm on pathology. Bland-Altman analysis demonstrated good agreement for tumor thickness (mean difference 0.2 mm; limits of agreement -5.5 to +5.5 mm) and acceptable agreement for base diameter (mean difference 3.4 mm; limits -8.2 to +15.1 mm). ICC indicated moderate agreement for base diameter (0.501) and excellent agreement for thickness (0.843). Pathological thickness correlated significantly with shorter metastasis-free survival ( r = -0.293, P  = 0.024). Kaplan-Meier analysis showed significantly poorer survival for patients with T3-T4 tumors. Ultrasonography provides a reliable preoperative estimation of choroidal melanoma size, particularly for tumor thickness, although histopathology remains essential for prognostication. Survival patterns in this cohort align with international data, highlighting the relevance of tumor thickness and morphology and emphasizing the value of data from an underrepresented region.

脉络膜黑色素瘤的超声和组织病理学相关性:来自塞尔维亚单中心研究的生存结果。
比较超声和组织病理学测量的肿瘤大小的无核眼脉络膜黑色素瘤,并评估肿瘤大小和形态特征的预后意义在塞尔维亚队列。本回顾性研究纳入了59例连续在塞尔维亚临床中心大学眼科医院接受组织病理学证实的脉络膜黑色素瘤摘除手术的患者。所有超声检查、外科手术和组织病理学评估均由专门的专科医生完成。术前b超测量肿瘤基底直径和厚度,并与术后宏观组织病理尺寸进行配对统计检验、Bland-Altman分析和类内相关系数(ICC)比较。采用Pearson和Spearman相关性及Kaplan-Meier分析评估生存结果。对患者进行了至少1年的随访,其中一些患者的监测时间长达5年。数据以mean±SD表示。超声图平均基底直径为14.63±3.98 mm,厚度为10.34±3.54 mm,病理图平均基底直径为18.04±6.54 mm,厚度为10.55±3.72 mm。Bland-Altman分析显示肿瘤厚度(平均差值0.2 mm,差值-5.5至+5.5 mm)和基底直径(差值3.4 mm,差值-8.2至+15.1 mm)的一致性良好。ICC显示,基底直径的一致性中等(0.501),厚度的一致性极佳(0.843)。病理厚度与较短的无转移生存期显著相关(r = -0.293, P = 0.024)。Kaplan-Meier分析显示T3-T4肿瘤患者的生存率明显较低。超声检查提供了一个可靠的术前估计脉络膜黑色素瘤的大小,特别是肿瘤的厚度,尽管组织病理学仍然是必不可少的预后。该队列的生存模式与国际数据一致,突出了肿瘤厚度和形态的相关性,并强调了来自代表性不足地区的数据的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Melanoma Research
Melanoma Research 医学-皮肤病学
CiteScore
3.40
自引率
4.50%
发文量
139
审稿时长
6-12 weeks
期刊介绍: ​​​​​​Melanoma Research is a well established international forum for the dissemination of new findings relating to melanoma. The aim of the Journal is to promote the level of informational exchange between those engaged in the field. Melanoma Research aims to encourage an informed and balanced view of experimental and clinical research and extend and stimulate communication and exchange of knowledge between investigators with differing areas of expertise. This will foster the development of translational research. The reporting of new clinical results and the effect and toxicity of new therapeutic agents and immunotherapy will be given emphasis by rapid publication of Short Communications. ​Thus, Melanoma Research seeks to present a coherent and up-to-date account of all aspects of investigations pertinent to melanoma. Consequently the scope of the Journal is broad, embracing the entire range of studies from fundamental and applied research in such subject areas as genetics, molecular biology, biochemistry, cell biology, photobiology, pathology, immunology, and advances in clinical oncology influencing the prevention, diagnosis and treatment of melanoma.
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