Chen Tingrui, Wu Xiaoxiao, Wang Yiping
Department of ICU, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Front Cardiovasc Med. 2024 Jul 25;11:1391775. doi: 10.3389/fcvm.2024.1391775. eCollection 2024.
A 33-year-old patient presented with a chief complaint of patent ductus arteriosus (PDA) persisting for over 30 years. Physical examination revealed bilateral facial angiofibromas, multiple nail fibromas, intraoral fibromas, and a 'shagreen patch' on the left lumbar region. Genetic testing was performed using a peripheral venous blood sample, which confirmed the diagnosis of Tuberous Sclerosis Type 2 (TSC2). Subsequently, the patient underwent cardiac color Doppler ultrasound and chest computed tomography angiography, which confirmed the presence of PDA. Tuberous sclerosis complex (TSC) is associated with cardiovascular diseases. The initial clinical manifestation of TSC is usually cardiac rhabdomyoma in children, and it is rarely reported in adults with PDA. In this case, the patient was diagnosed with PDA when he was young, and the genetic test showed heterozygous variation of TSC2 gene. The purpose of this article is to explore the correlation between TSC and PDA at the gene level through literature review.
一名33岁患者,主诉动脉导管未闭(PDA)持续存在30余年。体格检查发现双侧面部血管纤维瘤、多发甲周纤维瘤、口腔内纤维瘤以及左侧腰部的“鲨革斑”。采用外周静脉血样本进行基因检测,确诊为2型结节性硬化症(TSC2)。随后,患者接受了心脏彩色多普勒超声和胸部计算机断层扫描血管造影,证实存在PDA。结节性硬化症复合体(TSC)与心血管疾病相关。TSC的初始临床表现通常在儿童中为心脏横纹肌瘤,而在患有PDA的成人中很少报道。在本病例中,患者年轻时被诊断为PDA,基因检测显示TSC2基因杂合变异。本文旨在通过文献综述探讨TSC与PDA在基因水平上的相关性。