• 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

结节性硬化症中心脏横纹肌瘤的自然消退

Spontaneous regression of cardiac rhabdomyoma in tuberous sclerosis.

作者信息

Alkalay A L, Ferry D A, Lin B, Fink B W, Pomerance J J

机构信息

Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA 90048.

出版信息

Clin Pediatr (Phila). 1987 Oct;26(10):532-5. doi: 10.1177/000992288702601008.

DOI:10.1177/000992288702601008
PMID:3308273
Abstract

Life-threatening cardiac rhabdomyoma in a newborn infant regressed spontaneously within a 5 month period. Since cardiac surgery for rhabdomyoma is dangerous in infancy, medical management should be considered if symptomatology is not severe. When a fetal arrhythmia is diagnosed, antenatal ultrasound examination for presence of cardiac tumors is warranted.

摘要

一名新生儿患有危及生命的心脏横纹肌瘤,该肿瘤在5个月内自行消退。由于婴儿期进行心脏横纹肌瘤手术具有危险性,若症状不严重,则应考虑药物治疗。当诊断出胎儿心律失常时,有必要进行产前超声检查以确定是否存在心脏肿瘤。

相似文献

1
Spontaneous regression of cardiac rhabdomyoma in tuberous sclerosis.结节性硬化症中心脏横纹肌瘤的自然消退
Clin Pediatr (Phila). 1987 Oct;26(10):532-5. doi: 10.1177/000992288702601008.
2
[Cardiac rhabdomyoma and apoptosis: are regression controlled by the body?].[心脏横纹肌瘤与细胞凋亡:其消退受机体控制吗?]
Arch Mal Coeur Vaiss. 1992 May;85(5):603-8.
3
Cardiac rhabdomyoma associated with tuberous sclerosis. An autopsy case of newborn infant died of cardiac failure.与结节性硬化症相关的心脏横纹肌瘤。一例死于心力衰竭的新生儿尸检病例。
Acta Pathol Jpn. 1987 Apr;37(4):645-53.
4
Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma.心脏横纹肌瘤患者中结节性硬化症的发病率。
Am J Med Genet. 1990 Dec;37(4):443-6. doi: 10.1002/ajmg.1320370402.
5
New-onset cardiac rhabdomyoma beyond infancy in a patient with tuberous sclerosis complex.一名患有结节性硬化症的患者在婴儿期后出现新发心脏横纹肌瘤。
Cardiol Young. 2016 Feb;26(2):396-9. doi: 10.1017/S1047951115001183. Epub 2015 Jul 14.
6
Paroxysmal supraventricular tachycardia in neonatal tuberous sclerosis complex and cardiac rhabdomyoma: report of one case.新生儿结节性硬化症合并心脏横纹肌瘤中的阵发性室上性心动过速:一例报告
Acta Paediatr Taiwan. 2003 Mar-Apr;44(2):112-5.
7
Cardiac rhabdomyoma in intrauterine life: clinical features and natural history. A case series and review of published reports.宫内生活中的心脏横纹肌瘤:临床特征与自然病史。病例系列及已发表报告综述。
Ital Heart J. 2002 Jan;3(1):48-52.
8
Cardiac rhabdomyoma in infancy.
Acta Paediatr Scand. 1974 Mar;63(2):283-6. doi: 10.1111/j.1651-2227.1974.tb04797.x.
9
Tuberous sclerosis with intracardiac rhabdomyoma in a fetus with trisomy 21: case report and review of literature.21三体胎儿合并心脏横纹肌瘤的结节性硬化症:病例报告及文献复习
Prenat Diagn. 1999 Jul;19(7):610-3. doi: 10.1002/(sici)1097-0223(199907)19:7<610::aid-pd596>3.0.co;2-q.
10
Coexistent cardiac rhabdomyoma with mitral valve anomaly in patients with tuberous sclerosis: a case report.结节性硬化症患者合并心脏横纹肌瘤与二尖瓣异常:一例报告
Thorac Cardiovasc Surg. 2007 Mar;55(2):120-1. doi: 10.1055/s-2006-924243.

引用本文的文献

1
Atypical mediastinal mass in the fetus: a review of the literature.胎儿非典型纵隔肿块:文献综述
Arch Gynecol Obstet. 2025 Feb;311(2):203-212. doi: 10.1007/s00404-024-07921-4. Epub 2025 Jan 15.
2
Regression of Cardiac Rhabdomyomas Producing a Severe Aortic Stenosis: Case Report and Discussion of the Literature.导致严重主动脉瓣狭窄的心脏横纹肌瘤消退:病例报告及文献讨论
Diagnostics (Basel). 2024 Feb 21;14(5):470. doi: 10.3390/diagnostics14050470.
3
ANTENATAL ULTRASOUND DIAGNOSIS OF CARDIAC RHABDOMYOMA IN ONE OF THE TWINS.
双胎之一心脏横纹肌瘤的产前超声诊断
Med J Armed Forces India. 2000 Oct;56(4):347-348. doi: 10.1016/S0377-1237(17)30229-0. Epub 2017 Jun 12.
4
Actin isoform expression patterns in adult extracardiac and cardiac rhabdomyomas indicate a different cell of origin.成人心脏外和心脏横纹肌瘤中肌动蛋白同工型表达模式表明其起源细胞不同。
Virchows Arch. 2017 Mar;470(3):285-290. doi: 10.1007/s00428-017-2069-3. Epub 2017 Jan 14.
5
Cardiac rhabdomyomas associated with tuberous sclerosis complex in children. From presentation to outcome.儿童结节性硬化症相关的心脏横纹肌瘤。从临床表现到预后。
Herz. 2015 Jun;40(4):675-8. doi: 10.1007/s00059-014-4078-1. Epub 2014 Mar 9.
6
Fetal arrhythmias associated with cardiac rhabdomyomas.胎儿心律失常与心脏横纹肌瘤相关。
Heart Rhythm. 2014 Apr;11(4):677-83. doi: 10.1016/j.hrthm.2013.12.018. Epub 2013 Dec 11.
7
Cardiac rhabdomyoma in familial tuberous sclerosis.家族性结节性硬化症中的心脏横纹肌瘤
J Cardiovasc Thorac Res. 2013;5(2):71-2. doi: 10.5681/jcvtr.2013.015. Epub 2013 Jun 27.
8
Sudden death as presenting symptom caused by cardiac primary multicentric left ventricle rhabdomyoma, in an 11-month-old baby. An immunohistochemical study.11 个月大婴儿以心脏原发性多中心左心室横纹肌瘤为首发表现的猝死。免疫组化研究。
Diagn Pathol. 2012 Dec 3;7:169. doi: 10.1186/1746-1596-7-169.
9
Spontaneous regression of huge cardiac rhabdomyoma in an infant.婴儿巨大心脏横纹肌瘤的自发消退
Images Paediatr Cardiol. 2000 Oct;2(4):4-10.
10
Giant right atrial cystic hamartoma: a case report and literature review.巨大右房囊性错构瘤:一例报告及文献复习
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.02.2009.1587. Epub 2009 Jun 1.