The ability of prenatal cell-free DNA sequencing to incidentally detect occult maternal malignancies was first documented over a decade ago, yet coordinated follow-up of pregnant people who receive these results is still lacking in many countries. Here we provide a call to action for oncologists to become more involved in diagnosing and managing these cases..

十多年前首次记录了产前无细胞DNA测序偶然检测隐匿性母体恶性肿瘤的能力，但许多国家仍然缺乏对接受这些结果的孕妇进行协调的随访。在这里，我们呼吁肿瘤学家更多地参与诊断和管理这些病例。。

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Fig. 1: Cancers detected by prenatal cell-free DNA sequencing.

图1：通过产前无细胞DNA测序检测到的癌症。

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Download referencesAuthor informationAuthors and AffiliationsPrenatal Genomics & Therapy Section, Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD, USAAmy E. Turriff & Diana W. BianchiOffice of the Director, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD, USADiana W.

下载参考文献作者信息作者和附属机构美国国立卫生研究院国家人类基因组研究所精密健康研究中心基因组学与治疗科，美国马里兰州贝塞斯达，美国艾米·E·图里夫和黛安娜·W·比安奇美国国立卫生研究院尤妮丝·肯尼迪·施赖弗国家儿童健康与人类发展研究所所长办公室，美国马里兰州贝塞斯达，美国黛安娜·W。

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Rights and permissionsReprints and permissionsAbout this articleCite this articleTurriff, A.E., Bianchi, D.W. Oncologists must act to manage cancer detected through prenatal screening.

权利和许可打印和许可本文引用本文Turriff，A.E.，Bianchi，D.W。肿瘤学家必须采取行动来管理通过产前筛查发现的癌症。

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