PIK3CA-Related Overgrowth Spectrum

K. Keppler-Noreuil
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引用次数: 20

Abstract

Postzygotic mutations of the PIK3CA gene are associated with a series of clinical phenotypes characterized by segmental overgrowth and recently grouped under the term PIK3CA-related overgrowth spectrum (PROS). This chapter provides an overview of the clinical features shared by the phenotypes in PROS, including both the conditions with isolated features and the ones with syndromal presentation. The somatic overgrowth in cases with PROS is asymmetric, progressive, and “ballooning” in appearance and tends to involve predominantly the limbs, including fingers and toes, although the trunk and face are often affected as well. The tissues affected in the overgrowth can include all or some of these types: fibrous, adipose, vascular, nervous, and skeletal. Somatic gain-of-function mutations of PIK3CA cause activation of the PI3K-AKT pathway, leading to excessive cell growth and proliferation. Timing of PIK3CA mutations, tissue specificity, and type of mutation may play a role in the phenotypic variability of PROS.
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与pik3ca相关的过度生长谱
PIK3CA基因的合子后突变与一系列以片段过度生长为特征的临床表型相关,最近被归类为PIK3CA相关过度生长谱(PROS)。本章概述了pro中表型共有的临床特征,包括具有孤立特征的条件和具有综合征表现的条件。PROS病例的躯体过度生长是不对称的,进行性的,外观呈“气球状”,通常主要累及四肢,包括手指和脚趾,尽管躯干和面部也经常受到影响。在过度生长中受影响的组织可以包括所有或某些类型:纤维,脂肪,血管,神经和骨骼。PIK3CA的体细胞功能获得突变会激活PI3K-AKT通路,导致细胞过度生长和增殖。PIK3CA突变的时间、组织特异性和突变类型可能在PROS的表型变异性中发挥作用。
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