Genetic Profile of Arteriovenous Anomalies of the Head and Neck: Implications in Progression and Therapeutic Approaches

医学 克拉斯 动静脉畸形 头颈部 回顾性队列研究 放射科 内科学 外科 癌症 结直肠癌
作者
Marta María Pampín Martínez,Lara Rodríguez‐Laguna,Elena Gómez García,José Luis Cebrián Carretero,Teresa González Otero,Juan Carlos López‐Gutiérrez
出处
期刊:Journal of Pediatric Surgery [Elsevier BV]
卷期号:58 (10): 2043-2049 被引量:1
标识
DOI:10.1016/j.jpedsurg.2023.01.047
摘要

Background Arteriovenous Malformations (AVMs) are complex vascular anomalies that are usually sporadic and can have a variable clinical course. Treatment of AVMs can lead to severe sequeale and require thorough decision-making. There is a lack of standardized treatment protocols showing a growing need for pharmacological targeted therapies, specially in the most severe cases where surgery may not be feasible. Current knowledge in molecular pathways and genetic diagnosis have shed light in the pathophysiology of AVMs, opening possibilities for personalized treatment strategies. Methods We performed a retrospective review of patients with head and neck AVMs treated in our department between 2003 and 2021 and performed a complete physical examination and imaging with ultrasound and angio-CT or MRI. Patients underwent genetic testing on AVMs’ tissue samples and/or peripheral blood samples. Patients were grouped according to the genetic variant and a correlation between phenotype and genotype was studied. Results 22 patients with head and neck AVMs were included. We found eight patients with varians in MAP2K1, four patients with pathogenic variants in KRAS, six patients with pathogenic variants in RASA1, one patient with a pathogenic variant in BRAF, one patient with a pathogenic variant in NF1, another patient with a pathogenic variant in CELSR1 and one patient with pathogenic variants in PIK3CA and GNA14. Patients with MAP2K1 variants were the biggest group, with a moderate clinical course. Patients with KRAS mutations showed the most aggressive clinical course and a high rate of recurrence and osteolysis. Patients with RASA1 variants showed a characteristic phenotype with an ipsilateral capillary malformation in the neck. Conclusion We found a correlation between genotype and phenotype in this group of patients. The genetic diagnosis of AVMs is recommended in order to stablish a personalized treatment strategy. Targeted therapies are currently being investigated with promising results and may be recommended in addition to conventional surgical or embolization procedures, specially in the most complex cases. Level of evidence Level IV.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
1秒前
2秒前
3秒前
阿云发布了新的文献求助10
4秒前
TheDing完成签到,获得积分10
4秒前
FashionBoy应助xuexue0001采纳,获得10
5秒前
5秒前
RICK完成签到,获得积分10
7秒前
JW发布了新的文献求助10
7秒前
大力的飞莲完成签到,获得积分10
7秒前
JamesPei应助剪影改采纳,获得10
7秒前
cupid_lu发布了新的文献求助10
7秒前
woods发布了新的文献求助10
8秒前
我是站长才怪给achenghn的求助进行了留言
9秒前
SSSstriker完成签到,获得积分10
11秒前
11秒前
二一而已完成签到 ,获得积分10
12秒前
科研通AI2S应助科研通管家采纳,获得10
12秒前
douKY应助科研通管家采纳,获得10
12秒前
12秒前
12秒前
小雯钱来完成签到,获得积分10
13秒前
简单沛山完成签到,获得积分10
14秒前
sunshine完成签到,获得积分10
15秒前
15秒前
Orange应助gaochanglu采纳,获得10
16秒前
剪影改发布了新的文献求助10
16秒前
18秒前
凌宇完成签到 ,获得积分10
19秒前
脑洞疼应助Estella采纳,获得50
20秒前
周周发布了新的文献求助30
20秒前
Hello应助少一点丶天分采纳,获得10
21秒前
研友_VZG7GZ应助dayueban采纳,获得30
22秒前
22秒前
23秒前
夜倾心完成签到,获得积分10
23秒前
23秒前
呆呆棵发布了新的文献求助10
23秒前
23秒前
高分求助中
Les Mantodea de Guyane Insecta, Polyneoptera 2500
Nucleophilic substitution in azasydnone-modified dinitroanisoles 500
Technologies supporting mass customization of apparel: A pilot project 450
Brain and Heart The Triumphs and Struggles of a Pediatric Neurosurgeon 400
Cybersecurity Blueprint – Transitioning to Tech 400
Mixing the elements of mass customisation 400
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3783737
求助须知:如何正确求助?哪些是违规求助? 3328914
关于积分的说明 10239295
捐赠科研通 3044388
什么是DOI,文献DOI怎么找? 1670975
邀请新用户注册赠送积分活动 799997
科研通“疑难数据库(出版商)”最低求助积分说明 759172