Suppr超能文献

儿童结节性硬化症相关的肾血管平滑肌脂肪瘤。

Pediatric Renal Angiomyolipomas in Tuberous Sclerosis Complex.

机构信息

Department of Surgery, Division of Urology, University of Colorado School of Medicine, Aurora, Colorado; Department of Radiology, Division of Interventional Radiology (KLK), University of Colorado School of Medicine, Aurora, Colorado.

Department of Surgery, Division of Urology, University of Colorado School of Medicine, Aurora, Colorado; Department of Radiology, Division of Interventional Radiology (KLK), University of Colorado School of Medicine, Aurora, Colorado.

出版信息

J Urol. 2017 Feb;197(2):500-506. doi: 10.1016/j.juro.2016.09.082. Epub 2016 Sep 25.

Abstract

PURPOSE

Tuberous sclerosis complex is a genetic disorder characterized by the growth of hamartomas in multiple organs. Up to 80% of patients with tuberous sclerosis complex will have at least 1 angiomyolipoma in their lifetime. We describe the incidence and natural history of angiomyolipoma in a pediatric tuberous sclerosis complex population and analyze tumor growth to determine optimal renal imaging intervals in an effort to improve counseling, treatment and followup.

MATERIALS AND METHODS

We performed a retrospective chart review of all patients with tuberous sclerosis complex from 2004 to 2014. Patients were included if they had a clinical or genetic diagnosis of tuberous sclerosis complex and had undergone at least 1 renal imaging study.

RESULTS

A total of 145 patients were analyzed. Median age was 14 years (range 0 to 28). Overall incidence of angiomyolipoma was 50.3%. Median age at first angiomyolipoma detection was 11 years (range 2 to 26). Median yearly angiomyolipoma growth rate stratified by age at first detection was 0.0 mm for patients 0 to 6 years old, 0.9 mm for those 7 to 11 years old, 2.5 mm for those 12 to 16 years old and 1.8 mm for those 17 years old or older. Median yearly angiomyolipoma growth rate stratified by tumor size at first detection was 0.1 mm for tumors 0.6 to 0.9 cm, 1.8 mm for those 1.0 to 1.9 cm and 4.3 mm for those 2.0 to 2.9 cm. A total of 35 patients (24.1%) received mTOR (mammalian target of rapamycin) inhibitors. Eight patients underwent a total of 13 surgical interventions, of whom 2 had previously been treated with mTOR inhibitors. Median patient age at surgical intervention was 18.0 years and median angiomyolipoma size was 5.0 cm.

CONCLUSIONS

Angiomyolipoma growth in children with tuberous sclerosis complex can be rapid and unpredictable. We recommend yearly renal ultrasound in all patients with tuberous sclerosis complex, with consideration of magnetic resonance imaging in those at risk for rapid growth and future intervention (ie those older than 11 years and/or those with renal angiomyolipomas larger than 2 cm).

摘要

目的

结节性硬化症是一种遗传疾病,其特征是多种器官中出现错构瘤。多达 80%的结节性硬化症患者一生中至少会有 1 个血管平滑肌脂肪瘤。我们描述了儿科结节性硬化症人群中血管平滑肌脂肪瘤的发生率和自然病史,并分析了肿瘤的生长情况,以确定最佳的肾脏影像学检查间隔,从而改善咨询、治疗和随访。

材料和方法

我们对 2004 年至 2014 年间所有患有结节性硬化症的患者进行了回顾性图表审查。如果患者有临床或基因诊断为结节性硬化症,并至少进行了 1 次肾脏影像学研究,则将其纳入研究。

结果

共分析了 145 名患者。中位年龄为 14 岁(范围 0 至 28 岁)。血管平滑肌脂肪瘤的总发生率为 50.3%。首次发现血管平滑肌脂肪瘤的中位年龄为 11 岁(范围 2 至 26 岁)。按首次发现年龄分层的血管平滑肌脂肪瘤每年生长率的中位数为 0 至 6 岁患者为 0.0mm,7 至 11 岁患者为 0.9mm,12 至 16 岁患者为 2.5mm,17 岁或以上患者为 1.8mm。按首次发现时肿瘤大小分层的血管平滑肌脂肪瘤每年生长率的中位数为 0.6 至 0.9cm 的肿瘤为 0.1mm,1.0 至 1.9cm 的肿瘤为 1.8mm,2.0 至 2.9cm 的肿瘤为 4.3mm。共有 35 名患者(24.1%)接受了 mTOR(哺乳动物雷帕霉素靶蛋白)抑制剂治疗。8 名患者总共进行了 13 次手术干预,其中 2 名患者此前曾接受过 mTOR 抑制剂治疗。手术干预时患者的中位年龄为 18.0 岁,血管平滑肌脂肪瘤的中位大小为 5.0cm。

结论

结节性硬化症儿童的血管平滑肌脂肪瘤生长可能迅速且不可预测。我们建议对所有结节性硬化症患者每年进行肾脏超声检查,并考虑对生长迅速和有未来干预风险的患者(即年龄大于 11 岁和/或肾脏血管平滑肌脂肪瘤大于 2cm 的患者)进行磁共振成像检查。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验