Hiding in Plain Sight: Radiologic and Pathologic Findings Can Identify Beckwith-Wiedemann Syndrome in Patients With Wilms Tumor.

IF 0.9 4区 医学 Q4 HEMATOLOGY Journal of Pediatric Hematology/Oncology Pub Date : 2024-11-01 Epub Date: 2024-10-14 DOI:10.1097/MPH.0000000000002951
Laura M Molina, Akhila Rao, Julia Meade, Judy H Squires, Svetlana A Yatsenko, Claudia M Salgado, Miguel Reyes-Múgica
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Abstract

Most pediatric specialists, including hematologists/oncologists, surgeons, radiologists, and pathologists, are familiar with the diagnosis and management of Wilms tumor (WT). However, it may be challenging to identify the underlying conditions causing cancer predisposition, which can change the management for the patient and potentially their entire family. In this paper, we present 3 cases of clinically suspected WT associated with Beckwith-Wiedemann syndrome (BWS). We review the radiologic and histologic findings to diagnose BWS. We also discuss the implications of a BWS diagnosis on the clinical management of WT and follow-up guidelines for BWS patients.

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隐藏在众目睽睽之下:放射学和病理学发现可识别 Wilms 肿瘤患者的 Beckwith-Wiedemann 综合征。
大多数儿科专家,包括血液/肿瘤专家、外科医生、放射科医生和病理学家,都熟悉 Wilms 肿瘤 (WT) 的诊断和治疗。然而,确定导致癌症易感性的潜在疾病可能具有挑战性,这可能会改变对患者及其整个家庭的管理。在本文中,我们介绍了 3 例临床怀疑与贝克维茨-韦德曼综合征(BWS)相关的 WT 病例。我们回顾了诊断 BWS 的放射学和组织学结果。我们还讨论了 BWS 诊断对 WT 临床治疗的影响以及 BWS 患者的随访指南。
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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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