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乌尔氏畸形的成功手术修复。

Successful surgical repair of Uhl's anomaly.

作者信息

Azhari Nawal, Assaqqat Mervat, Bulbul Ziad

机构信息

Maternity & Children Hospital, Jeddah, Saudi Arabia.

出版信息

Cardiol Young. 2002 Mar;12(2):192-5. doi: 10.1017/s1047951102000410.

DOI:10.1017/s1047951102000410
PMID:12018730
Abstract

We report a case of Uhl's anomaly in a 5-month-old cyanotic infant who presented with thromboembolic stroke and acute hemiparesis. The patient underwent successfully an initial surgical repair, which included exclusion of the right ventricle by patch closure of the tricuspid valve, atrial septectomy and construction of a bidirectional Glenn shunt. This was followed by successful construction of a total cavopulmonary connection.

摘要

我们报告了一例5个月大的青紫型婴儿患乌尔异常的病例，该婴儿出现血栓栓塞性中风和急性偏瘫。患者成功接受了初次手术修复，包括用补片关闭三尖瓣以排除右心室、房间隔切除术和双向格林分流术的构建。随后成功构建了全腔静脉肺动脉连接。

相似文献

1
Successful surgical repair of Uhl's anomaly.乌尔氏畸形的成功手术修复。
Cardiol Young. 2002 Mar;12(2):192-5. doi: 10.1017/s1047951102000410.
2
Surgical Options for Uhl's Anomaly.乌尔氏畸形的手术治疗方案
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Single ventricle strategy for Uhl's anomaly of the right ventricle.右心室 Uhl 畸形的单心室策略。
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4
Long-term survival of Uhl's anomaly with total cavopulmonary conversion.全腔肺转流术后乌尔氏畸形的长期存活情况
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Biventricular repair of hypoplastic right ventricle assisted by pulsatile bidirectional cavopulmonary anastomosis.搏动性双向腔肺吻合辅助下的右心室发育不全双心室修复术。
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Uhl's Anomaly in Adulthood.成人 Uhl 氏异常。
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Repair of isolated double-chambered right ventricle.
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Uhl's anomaly: perspective of fetal echocardiography and histopathological correlation.乌尔氏畸形：胎儿超声心动图视角与组织病理学相关性
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A rare case of partial absence of the right ventricular musculature in asymptomatic adult man: partial Uhl's anomaly.无症状成年男性右心室部分肌缺失 1 例：部分 Uhl 畸形。
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引用本文的文献

1
Heart Transplantation for Uhl Anomaly in an Adult.成人Uhl畸形的心脏移植
JACC Case Rep. 2024 Apr 4;29(10):102322. doi: 10.1016/j.jaccas.2024.102322. eCollection 2024 May 15.
2
Univentricular palliation for a child with severe Uhl's anomaly.为一名患有严重乌尔氏异常的儿童进行单心室姑息治疗。
JTCVS Tech. 2022 Apr 30;14:207-211. doi: 10.1016/j.xjtc.2022.04.026. eCollection 2022 Aug.
3
Uhl's Anomaly With Left Ventricular Noncompaction: Role of Multimodality Imaging in a Rare Association.乌尔畸形合并左心室心肌致密化不全：多模态成像在罕见关联中的作用
JACC Case Rep. 2021 Sep 15;3(12):1463-1467. doi: 10.1016/j.jaccas.2021.06.042.
4
A Case of Prenatally Diagnosed Uhl's Anomaly with Absent Pulmonary Valve Leaflets and Dysplastic Tricuspid Valve.一例产前诊断为乌尔氏畸形伴肺动脉瓣叶缺如及三尖瓣发育异常的病例。
Children (Basel). 2021 Mar 3;8(3):190. doi: 10.3390/children8030190.
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Large Right Ventricle Thrombus in Uhl's Anomaly: A Rare Presentation of Extremely Rare Disease.乌尔氏畸形中的巨大右心室血栓：一种极其罕见疾病的罕见表现。
Cardiol Res. 2019 Apr;10(2):124-127. doi: 10.14740/cr758w. Epub 2019 Apr 11.
6
Uhl's anomaly detected in-utero.子宫内检测到乌尔氏异常。
Australas J Ultrasound Med. 2014 Nov;17(4):150-152. doi: 10.1002/j.2205-0140.2014.tb00237.x. Epub 2015 Dec 31.
7
Uhl's anomaly: Absence of the right ventricular myocardium.乌尔氏异常：右心室心肌缺如。
Ann Pediatr Cardiol. 2015 Jan-Apr;8(1):71-3. doi: 10.4103/0974-2069.149529.