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遗传性胃肠道癌风险综合征中的儿科癌症筛查:AACR 儿童癌症易感性工作组的最新进展。

Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group.

机构信息

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Clin Cancer Res. 2024 Oct 15;30(20):4566-4571. doi: 10.1158/1078-0432.CCR-24-0953.

Abstract

Gastrointestinal (GI) polyposis and cancer in pediatric patients is frequently due to an underlying hereditary cancer risk syndrome requiring ongoing cancer screening. Identification of at-risk patients through family history, clinical features of a syndrome, or symptom onset ensures appropriate cancer risk assessment and management in childhood and beyond. In this 2024 perspective, we outline updates to the hereditary GI cancer screening guidelines first published by the American Association of Cancer Research Pediatric Cancer Predisposition Workshop in 2017. These guidelines consider existing recommendations by pediatric and adult gastroenterology consortia to ensure alignment with gastroenterology practices in managing polyposis conditions. We specifically address the recommendations for pediatric screening in familial adenomatous polyposis, Peutz-Jeghers syndrome, and juvenile polyposis syndrome. Further, we emphasize the importance of multidisciplinary care and partnership with gastroenterology, as it is crucial in management of children and families with these conditions.

摘要

儿童胃肠道(GI)息肉和癌症通常是由于潜在的遗传性癌症风险综合征引起的,需要进行持续的癌症筛查。通过家族史、综合征的临床特征或症状发作来识别高危患者,可确保在儿童期及以后进行适当的癌症风险评估和管理。在 2024 年的这一展望中,我们概述了美国癌症研究协会儿科癌症易感性研讨会于 2017 年首次发布的遗传性 GI 癌症筛查指南的更新。这些指南考虑了儿科和成人胃肠病学联盟的现有建议,以确保与管理息肉病的胃肠病学实践保持一致。我们特别针对家族性腺瘤性息肉病、Peutz-Jeghers 综合征和青少年息肉病综合征的儿科筛查建议进行了讨论。此外,我们强调多学科护理和与胃肠病学合作的重要性,因为这对于管理这些疾病的儿童和家庭至关重要。

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