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一例与孤立性右心室发育不全相关的右心房血栓形成病例。

A case of right atrial thrombosis associated with isolated right ventricular hypoplasia.

作者信息

Satokawa H, Iwaya F, Igari T, Hoshino S, Yamaguchi N, Maruyama Y

机构信息

Department of Cardiovascular Surgery, Fukushima Medical College, Japan.

出版信息

Fukushima J Med Sci. 1990 Dec;36(2):91-5.

PMID:2131289
Abstract

A rare case of right atrial thrombosis was observed in a 49-year-old woman. She had cyanotic ostium secundum atrial septal defect without pulmonary hypertension. By postoperative cardiac catheterization, she was diagnosed as having isolated right ventricular hypoplasia.

摘要

在一名49岁女性中观察到一例罕见的右心房血栓形成。她患有紫绀型继发孔房间隔缺损,无肺动脉高压。通过术后心导管检查,她被诊断为孤立性右心室发育不全。

相似文献

1
A case of right atrial thrombosis associated with isolated right ventricular hypoplasia.一例与孤立性右心室发育不全相关的右心房血栓形成病例。
Fukushima J Med Sci. 1990 Dec;36(2):91-5.
2
Prolonged survival despite severe cyanosis in an adult with right ventricular hypoplasia and atrial septal defect.一名患有右心室发育不全和房间隔缺损的成年人尽管出现严重紫绀但仍长期存活。
Am Heart J. 1990 Sep;120(3):701-3. doi: 10.1016/0002-8703(90)90035-v.
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Isolated hypoplasia of right ventricle with atrial septal defect: a rare form of cyanotic heart disease.孤立性右心室发育不全合并房间隔缺损:一种罕见的青紫型心脏病。
Indian Heart J. 1999 Jul-Aug;51(4):440-3.
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[Hypoplasia of the right ventricle and cyanosis due to left-right atrial shunt within the framework of Turner's syndrome. Surgical closing of the interatrial connection after occlusion testing with balloon catheterization].[特纳综合征框架下右心室发育不全及因左右心房分流导致的发绀。经球囊导管封堵试验后手术闭合房间隔连接]
Arch Mal Coeur Vaiss. 1983 Feb;76(2):233-7.
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[Isolated right ventricular hypoplasia].[孤立性右心室发育不全]
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Paradoxical embolism in the presence of right-to-left shunt due to tricuspid occlusion.由于三尖瓣闭塞导致右向左分流时的反常栓塞。
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[Coronary sinus atrial septal defect diagnosed by cyanosis after operation of ventricular septal defect].[室间隔缺损术后因青紫诊断出冠状窦型房间隔缺损]
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引用本文的文献

1
Clinical Status and Outcome of Isolated Right Ventricular Hypoplasia: A Systematic Review and Pooled Analysis of Case Reports.孤立性右心室发育不全的临床状况与结局:病例报告的系统评价与汇总分析
Front Pediatr. 2022 Apr 21;10:794053. doi: 10.3389/fped.2022.794053. eCollection 2022.