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结节性硬化症的肾脏表现。

Renal manifestation of tuberous sclerosis complex.

机构信息

Department of Pediatrics, University of Tennessee Health Science Center and Le Bonheur Children's Hospital, Memphis, TN.

St. Jude Children's Research Hospital, Memphis, TN.

出版信息

Am J Med Genet C Semin Med Genet. 2018 Sep;178(3):338-347. doi: 10.1002/ajmg.c.31654. Epub 2018 Oct 11.

Abstract

Tuberous sclerosis complex (TSC) is a tumor predisposition syndrome with significant renal cystic and solid tumor disease. It commonly causes several types of cystic disease and benign tumors (angiomyolipomata) in the kidneys that can both lead to significant premature loss of glomerular filtration rate. The main risks of angiomyolipomata, severe bleeding, loss of renal function, and pulmonary lymphangioleiomyomatosis, can be ameliorated by active surveillance and preemptive therapy with mTOR inhibitors. The cystogenic mechanism may involve primary cilia, but also appears to also involve a majority of normal tubular cells and may be driven by a minority of cells with mutations inactivating both their TSC1 or TSC2 genes. Malignant tumors are rare.

摘要

结节性硬化症(TSC)是一种肿瘤易感性综合征,伴有显著的肾脏囊性和实体肿瘤疾病。它通常会导致肾脏的几种囊性疾病和良性肿瘤(血管平滑肌脂肪瘤),这两者都可能导致肾小球滤过率过早显著丧失。血管平滑肌脂肪瘤的主要风险,包括严重出血、肾功能丧失和肺淋巴管平滑肌瘤病,可以通过积极的监测和使用 mTOR 抑制剂进行预防性治疗来缓解。囊性病变的发生机制可能涉及初级纤毛,但似乎也涉及大多数正常管状细胞,并且可能由少数具有 TSC1 或 TSC2 基因突变失活的细胞驱动。恶性肿瘤很少见。

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