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本文引用的文献

1
Rupture of the papillary muscle of the tricuspid valve - echocardiographic diagnosis of a rare anomaly leading to critical tricuspid valve regurgitation in the newborn.三尖瓣乳头肌断裂 - 导致新生儿严重三尖瓣反流的罕见畸形的超声心动图诊断。
Eur J Pediatr. 2010 Feb;169(2):165-6. doi: 10.1007/s00431-009-0996-y. Epub 2009 May 24.
2
A case of an infant with flail tricuspid valve due to spontaneous papillary muscle rupture: was neonatal lupus the culprit?一例因自发性乳头肌破裂导致连枷样三尖瓣的婴儿病例:新生儿狼疮是罪魁祸首吗?
Pediatr Cardiol. 2008 Mar;29(2):442-5. doi: 10.1007/s00246-007-9109-8. Epub 2007 Sep 20.
3
Neonatal mitral and tricuspid valve repair for in utero papillary muscle rupture.新生儿二尖瓣和三尖瓣修复术用于治疗胎儿期乳头肌破裂。
Ann Thorac Surg. 2007 Apr;83(4):1458-62. doi: 10.1016/j.athoracsur.2006.10.077.
4
Ruptured tricuspid valve papillary muscle: a treatable cause of neonatal cyanosis.三尖瓣乳头肌破裂:新生儿青紫的一个可治疗病因。
Ann Thorac Surg. 2007 Feb;83(2):680-2. doi: 10.1016/j.athoracsur.2006.06.054.
5
Successful repair of critical tricuspid regurgitation secondary to ruptured papillary muscle in a newborn.成功修复新生儿乳头肌破裂继发的严重三尖瓣反流。
Cardiol Young. 2004 Aug;14(4):450-2. doi: 10.1017/S1047951104004172.
6
Aberrant tendinous chords with tethering of the tricuspid leaflets: a congenital anomaly causing severe tricuspid regurgitation.伴有三尖瓣小叶系索的异常腱索:一种导致严重三尖瓣反流的先天性异常。
Heart. 2004 Mar;90(3):319-23. doi: 10.1136/hrt.2002.006254.
7
De Vega tricuspid annuloplasty for systemic tricuspid regurgitation in children with univentricular physiology.De Vega三尖瓣成形术治疗单心室生理儿童的系统性三尖瓣反流
J Heart Valve Dis. 2004 Jan;13(1):86-90.
8
Intrauterine left chamber myocardial infarction of the heart and hydrops fetalis in the recipient fetus due to twin-to-twin transfusion syndrome.由于双胎输血综合征,受血胎儿发生宫内左心室心肌梗死及胎儿水肿。
Prenat Diagn. 2002 Mar;22(3):241-3. doi: 10.1002/pd.302.
9
Immunohistochemical detection of myocardial necrosis in stillbirth and neonatal death.
Pediatr Dev Pathol. 2000 Jan-Feb;3(1):40-7. doi: 10.1007/s100240050005.
10
Surgical management of isolated congenital tricuspid regurgitation.
Ann Thorac Surg. 1998 Nov;66(5):1571-4. doi: 10.1016/s0003-4975(98)00753-x.

新生儿发绀的罕见病因。

Unusual cause of neonatal cyanosis.

作者信息

Abd El Rahman M Y, Al Qurashi M M, Al Khalifeh F A

机构信息

Division of Cardiology, Department of Pediatrics, Al Yamamah Hospital - Riyadh, Saudi Arabia.

出版信息

J Saudi Heart Assoc. 2011 Jan;23(1):45-7. doi: 10.1016/j.jsha.2010.09.002. Epub 2010 Oct 14.

DOI:10.1016/j.jsha.2010.09.002
PMID:23960635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3727387/
Abstract

We present a case of a full-term female neonate who presented at 6 h of age with severe cyanosis and was partially responsive to oxygen supplementation. An echocardiogram showed an isolated congenital severe tricuspid valve insufficiency due to rupture of the papillary muscle of the anterior tricuspid valve leaflet. Magnesium sulfate was infused to lower the pulmonary resistance and thus enhancing the antegrade pulmonary blood flow. Ductal patency was secured by prostaglandin infusion thus providing an additional pulmonary blood flow through the ductus arteriosus. The above measures were adequate to stabilize the patient with no further deterioration or the need for other supportive measures such as Nitric Oxide therapy or extracorporeal membrane oxygenation (ECMO). Therefore, early diagnosis and adequate measures to improve the pulmonary blood flow are mandatory, important pre-operative measures in the management of these patients.

摘要

我们报告一例足月女新生儿,出生6小时时出现严重青紫,吸氧后有部分反应。超声心动图显示,由于三尖瓣前叶乳头肌破裂导致孤立性先天性严重三尖瓣关闭不全。输注硫酸镁以降低肺阻力,从而增加肺前向血流量。通过输注前列腺素确保动脉导管通畅,从而通过动脉导管提供额外的肺血流量。上述措施足以使患者病情稳定,未进一步恶化,也无需其他支持措施,如一氧化氮治疗或体外膜肺氧合(ECMO)。因此,早期诊断和采取适当措施改善肺血流量是这些患者治疗中至关重要的术前措施。