Gestational trophoblastic disease: STR genotyping for precision diagnosis.

IF 3.9 3区 医学 Q1 PATHOLOGY
Krasimira A Rozenova, Natalia Buza, Pei Hui
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引用次数: 0

Abstract

Introduction: Gestational trophoblastic disease (GTD) encompasses a constellation of rare to common gynecologic conditions stemming from aberrant gestations with distinct genetic backgrounds and variable degrees of trophoblast proliferation of either neoplastic or non-neoplastic nature. GTD is categorized into hydatidiform moles and gestational trophoblastic neoplasms, and their clinical outcomes vary widely across different subtypes. Prompt and accurate diagnosis plays a pivotal role in the effective management and prognostication of patients. Short tandem repeats (STRs) are repetitive DNA sequences dispersed throughout the human genome and inherit a tremendous genetic polymorphism among individuals. Widely recognized for its applications in forensic identity and paternity testing, the relevance of STR genotyping in the diagnosis of GTD has emerged as an essential ancillary test in the classification and management of GTD of both non-neoplastic hydatidiform moles and gestational trophoblastic tumors.

Area covered: This review discusses fundamental principles, laboratory operation, and diagnostic interpretations of STR genotyping in the context of diagnosis and differential diagnosis of GTD. PubMed was searched for all references up to 2024.

Expert opinion: STR genotyping is the gold standard in the diagnosis and subclassification of hydatidiform moles and has an important application in diagnostic workup and risk stratifications of gestational trophoblastic tumors as well.

妊娠滋养细胞疾病:STR基因分型用于精确诊断。
妊娠滋养细胞疾病(GTD)包括一系列罕见到常见的妇科疾病,这些疾病源于异常妊娠,具有不同的遗传背景和不同程度的滋养细胞增殖,无论是肿瘤还是非肿瘤性质。GTD分为葡萄胎样痣和妊娠滋养细胞肿瘤,不同亚型的临床结果差异很大。及时准确的诊断对患者的有效治疗和预后起着关键作用。短串联重复序列(STRs)是分散在人类基因组中的重复DNA序列,在个体之间具有巨大的遗传多态性。STR基因分型在GTD诊断中的相关性已成为非肿瘤性包体痣和妊娠滋养细胞肿瘤的GTD分类和治疗中必不可少的辅助检测,其在法医鉴定和亲子鉴定中的应用已得到广泛认可。涉及领域:本文综述了STR基因分型在GTD诊断和鉴别诊断中的基本原理、实验室操作和诊断解释。PubMed检索了截至2024年的所有参考文献。专家意见:STR基因分型是包体痣诊断和分型的金标准,也是妊娠滋养细胞肿瘤诊断检查和风险分层的重要应用。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
71
审稿时长
1 months
期刊介绍: Expert Review of Molecular Diagnostics (ISSN 1473-7159) publishes expert reviews of the latest advancements in the field of molecular diagnostics including the detection and monitoring of the molecular causes of disease that are being translated into groundbreaking diagnostic and prognostic technologies to be used in the clinical diagnostic setting. Each issue of Expert Review of Molecular Diagnostics contains leading reviews on current and emerging topics relating to molecular diagnostics, subject to a rigorous peer review process; editorials discussing contentious issues in the field; diagnostic profiles featuring independent, expert evaluations of diagnostic tests; meeting reports of recent molecular diagnostics conferences and key paper evaluations featuring assessments of significant, recently published articles from specialists in molecular diagnostic therapy. Expert Review of Molecular Diagnostics provides the forum for reporting the critical advances being made in this ever-expanding field, as well as the major challenges ahead in their clinical implementation. The journal delivers this information in concise, at-a-glance article formats: invaluable to a time-constrained community.
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