Suppr超能文献

神经脂肪瘤病伴或不伴神经区域过度生长中 PIK3CA 突变。

PIK3CA mutations in lipomatosis of nerve with or without nerve territory overgrowth.

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Department of Neurosurgery, Mayo Clinic, Rochester, MN, USA.

出版信息

Mod Pathol. 2020 Mar;33(3):420-430. doi: 10.1038/s41379-019-0354-1. Epub 2019 Sep 3.

Abstract

Lipomatosis of nerve is a rare malformation characterized by a fibrolipomatous proliferation within peripheral nerve. Lipomatosis of nerve most frequently involves the median nerve, and manifests clinically as a compressive neuropathy. However, 30-60% of cases are associated with tissue overgrowth within the affected nerve's territory (e.g., macrodactyly for lipomatosis of nerve in the distal median nerve). Somatic activating PIK3CA mutations have been identified in peripheral nerve from patients with lipomatosis of nerve with type I macrodactyly, which is now classified as a PIK3CA-related overgrowth spectrum disorder. However, the PIK3CA mutation status of histologically confirmed lipomatosis of nerve, including cases involving proximal nerves, and cases without territory overgrowth, has not been determined. Fourteen histologically confirmed cases of lipomatosis of nerve involving the median (N = 6), brachial plexus (N = 1), ulnar (N = 3), plantar (N = 2), sciatic and superficial peroneal nerves (N = 1 each) were included. Ten cases had nerve territory overgrowth, ranging from macrodactyly to hemihypertrophy; and four cases had no territory overgrowth. Exome sequencing revealed "hotspot" activating PIK3CA missense mutations in 6/7 cases. Droplet digital polymerase chain reaction for the five most common PIK3CA mutations (p.H1047R, p.H1047L, p.E545K, p.E542K, and p.C420R) confirmed the exome results and identified an additional six cases with mutations (12/14 total). PIK3CA mutations were found in 8/10 cases with territory overgrowth (N = 7 p.H1047R and N = 1 p.E545K), including two proximal nerve cases with extremity overgrowth, and 4/4 cases without territory overgrowth (p.H1047R and p.H1047L, N = 2 each). The variant allele frequency of PIK3CA mutations (6-32%) did not correlate with the overgrowth phenotype. Three intraneural lipomas had no detected PIK3CA mutations. As PIK3CA mutations are frequent events in lipomatosis of nerve, irrespective of anatomic site or territory overgrowth, we propose that all phenotypic variants of this entity be classified within the PIK3CA-related overgrowth spectrum and termed "PIK3CA-related lipomatosis of nerve".

摘要

神经脂肪瘤病是一种罕见的畸形,其特征是周围神经内出现纤维脂肪瘤增生。神经脂肪瘤病最常累及正中神经,临床上表现为压迫性神经病。然而,30-60%的病例与受累神经区域内的组织过度生长有关(例如,远端正中神经的神经脂肪瘤病引起的巨指症)。在具有 I 型巨指症的神经脂肪瘤病患者的周围神经中,已经发现了体细胞激活的 PIK3CA 突变,现在将其归类为 PIK3CA 相关过度生长谱障碍。然而,组织学证实的神经脂肪瘤病(包括涉及近端神经的病例和无区域过度生长的病例)的 PIK3CA 突变状态尚未确定。本研究纳入了 14 例组织学证实的正中神经(N=6)、臂丛(N=1)、尺神经(N=3)、足底(N=2)、坐骨和腓浅神经(N=1 例)受累的神经脂肪瘤病。10 例有神经区域过度生长,范围从巨指症到半侧肥大;4 例无区域过度生长。外显子组测序在 6/7 例中发现了“热点”激活 PIK3CA 错义突变。用于五种最常见的 PIK3CA 突变(p.H1047R、p.H1047L、p.E545K、p.E542K 和 p.C420R)的数字聚合酶链反应(droplet digital polymerase chain reaction)确认了外显子组的结果,并发现了另外 6 例突变(共 14 例)。在有区域过度生长的 10 例中(N=7 p.H1047R 和 N=1 p.E545K),8 例(N=10)发现了 PIK3CA 突变,包括 2 例有肢体过度生长的近端神经病例和 4 例无区域过度生长的病例(p.H1047R 和 p.H1047L,N=2 例)。PIK3CA 突变的等位基因变异频率(6-32%)与过度生长表型无关。3 例神经内脂肪瘤未检测到 PIK3CA 突变。由于 PIK3CA 突变是神经脂肪瘤病中常见的事件,与解剖部位或区域过度生长无关,我们建议将该实体的所有表型变异归类为 PIK3CA 相关过度生长谱,并命名为“PIK3CA 相关神经脂肪瘤病”。

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