• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

先天性甲状腺功能减退症患儿的心脏畸形。

Cardiac malformations in children with congenital hypothyroidism.

机构信息

Pediatric Unit, Department of Science of Health, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Department of Human Pathology in Adult and Developmental Age "Gaetano Barresi", Unit of Emergency Pediatrics, University of Messina, "G. Martino" Policlinic, Italy.

出版信息

J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):91-97. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY.

PMID:33000607
Abstract

Congenital hypothyroidism (CH) is the most common endocrine disease in children, according to literature, infants with CH have an increased risk of associated congenital malformations (CM), especially cardiac defects (CD), compared to the general population. We retrospectively analyzed medical records of 255 patients with a positive screening result for CH in the period 1991-2016 followed at our Center. At the time of enrollment, the clinical examination included looking for the presence of heart murmurs and dysmorphic features. In all patients an echocardiography with cardiological evaluation were performed. Of all patients, 191 were included in the final analysis. Of these, 51.3% (98/191) presented an eutopic normally sized thyroid gland while 48.7% (93/191) showed a thyroid dysgenesis. Among the studied infants, 13.6% (26/191) presented CD. The most frequent cardiac anomaly was atrial septal defect (ASD) which was found in 65.4% (17/26) of patients with CD. Other defects were ventricular septal defect (VSD), patent ductus arteriosus (PDA), pulmonary valve stenosis (PvS), transposition of the great vessels (TGV), aortic valve stenosis (AvS). Six patients had multiple defects. In the analysed group, there was no significant relation with sex, type of CH, median blood-TSH (b-TSH) and serum-TSH (s-TSH) values and frequency of CD. There is a high prevalence of CD in CH, indicating the need of routine echocardiography in these patients to achieve an early diagnosis and management of CD.

摘要

先天性甲状腺功能减退症(CH)是儿童中最常见的内分泌疾病,根据文献报道,与一般人群相比,患有 CH 的婴儿发生先天性畸形(CM)的风险增加,尤其是心脏缺陷(CD)。我们回顾性分析了 1991 年至 2016 年在我们中心接受治疗的 255 例 CH 阳性筛查结果患者的病历。在入组时,临床检查包括寻找心脏杂音和畸形特征的存在。所有患者均进行了超声心动图和心脏评估。在所有患者中,有 191 例患者纳入最终分析。其中,51.3%(98/191)存在正常位置的甲状腺,而 48.7%(93/191)存在甲状腺发育不良。在所研究的婴儿中,13.6%(26/191)存在 CD。最常见的心脏异常是房间隔缺损(ASD),在 65.4%(17/26)的 CD 患者中发现。其他缺陷包括室间隔缺损(VSD)、动脉导管未闭(PDA)、肺动脉瓣狭窄(PvS)、大动脉转位(TGV)、主动脉瓣狭窄(AvS)。有 6 例患者存在多种缺陷。在分析组中,CD 与性别、CH 类型、中位血促甲状腺激素(b-TSH)和血清促甲状腺激素(s-TSH)值以及 CD 的频率均无显著相关性。CH 患者 CD 的患病率较高,表明需要对这些患者进行常规超声心动图检查,以实现 CD 的早期诊断和治疗。

相似文献

1
Cardiac malformations in children with congenital hypothyroidism.先天性甲状腺功能减退症患儿的心脏畸形。
J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):91-97. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY.
2
Evolution of congenital hypothyroidism in a cohort of preterm born children.早产儿队列中先天性甲状腺功能减退症的演变。
Pediatr Neonatol. 2020 Dec;61(6):629-636. doi: 10.1016/j.pedneo.2020.07.014. Epub 2020 Jul 23.
3
Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects.先天性甲状腺功能减退症伴发出生缺陷的墨西哥新生儿甲状腺发育不全发生率较高。
Early Hum Dev. 2012 Jan;88(1):61-4. doi: 10.1016/j.earlhumdev.2011.07.009. Epub 2011 Aug 3.
4
Survival analysis of Down syndrome with congenital heart disease: a 5-years registry at QSNICH.唐氏综合征合并先天性心脏病的生存分析:QSNICH的5年登记研究
J Med Assoc Thai. 2014 Jun;97 Suppl 6:S108-14.
5
High prevalence of associated birth defects in congenital hypothyroidism.先天性甲状腺功能减退症中相关出生缺陷的高患病率。
Int J Pediatr Endocrinol. 2010;2010:940980. doi: 10.1155/2010/940980. Epub 2010 May 4.
6
Cardiac arrest and ventricular arrhythmia in adults with Ebstein anomaly and left ventricular non-compaction.患有埃布斯坦畸形和左心室心肌致密化不全的成人发生心脏骤停和室性心律失常。
J Cardiol. 2018 May;71(5):484-487. doi: 10.1016/j.jjcc.2017.11.012. Epub 2018 Jan 2.
7
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.先天性甲状腺功能减退症由于甲状腺发育缺陷和筛查时 TSH 轻度升高:来自意大利先天性甲状腺功能减退症婴儿国家登记处的数据。
J Clin Endocrinol Metab. 2013 Apr;98(4):1403-8. doi: 10.1210/jc.2012-3273. Epub 2013 Feb 26.
8
Prevalence of minor musculoskeletal anomalies in children with congenital hypothyroidism.先天性甲状腺功能减退症患儿轻度肌肉骨骼异常的患病率。
Horm Res. 2007;68(6):272-5. doi: 10.1159/000104175. Epub 2007 Jun 20.
9
Congenital heart defects in patients with isolated microtia: evaluation using colour Doppler echocardiographic image.孤立性小耳畸形患者的先天性心脏缺陷:使用彩色多普勒超声心动图图像进行评估
Cardiol Young. 2021 Feb;31(2):260-263. doi: 10.1017/S104795112000387X. Epub 2020 Nov 17.
10
[Echocardiographic evaluation in unoperated congenital heart disease in adults].[成人未经手术治疗的先天性心脏病的超声心动图评估]
Herz. 1999 Jun;24(4):276-92. doi: 10.1007/BF03043879.

引用本文的文献

1
Primary congenital hypothyroidism: a clinical review.原发性先天性甲状腺功能减退症:临床综述
Front Endocrinol (Lausanne). 2025 Aug 5;16:1592655. doi: 10.3389/fendo.2025.1592655. eCollection 2025.
2
Growth Failure in Children with Congenital Heart Disease.先天性心脏病患儿的生长发育迟缓
Children (Basel). 2025 May 9;12(5):616. doi: 10.3390/children12050616.
3
Hypothyroidism in Patients with Down Syndrome: Prevalence and Association with Congenital Heart Defects.唐氏综合征患者的甲状腺功能减退症:患病率及其与先天性心脏病的关联。
Children (Basel). 2024 Apr 25;11(5):513. doi: 10.3390/children11050513.
4
Serological Characteristics, Etiological Analysis, and Treatment Prognosis of Children with Congenital Hypothyroidism.先天性甲状腺功能减退症患儿的血清学特征、病因分析及治疗预后
Emerg Med Int. 2022 Sep 27;2022:8005848. doi: 10.1155/2022/8005848. eCollection 2022.
5
Patent ductus arteriosus in a late preterm neonate: think congenital hypopituitarism.晚早产儿动脉导管未闭:要考虑先天性垂体功能减退症。
BMJ Case Rep. 2022 Aug 18;15(8):e248188. doi: 10.1136/bcr-2021-248188.