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一名患有顽固性持续胎儿循环的新生儿的三尖瓣乳头肌破裂

Ruptured Tricuspid Valve Papillary Muscle in a Neonate with Intractable Persistent Fetal Circulation.

作者信息

Yoon Ja Kyoung, Kim Hye Rim, Kwon Hye Won, Kwon Bo Sang, Kim Gi Beom, Bae Eun Jung, Noh Chung Il, Kim Woong Han

机构信息

Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.

Department of Thoracic & Cardiovascular Surgery, Seoul National University Children's Hospital, Seoul, Korea.

出版信息

Korean Circ J. 2015 Jul;45(4):340-3. doi: 10.4070/kcj.2015.45.4.340. Epub 2015 Jun 5.

Abstract

Unguarded tricuspid regurgitation (TR) due to a flail tricuspid leaflet is a rare condition of newborn cyanosis. A high perinatal mortality has been associated with this fatal condition. But, there are feasible surgical repairs to improve survival. We report the case of a male full-term neonate with intractable hypoxia. He had profound tricuspid insufficiency and leaflet prolapse caused by a ruptured papillary muscle supporting the anterior leaflet of the tricuspid valve. He presented with severe cyanosis and respiratory distress immediately after birth. Despite medical management, the pulmonary vascular resistance was not decreased and a low cardiac output persisted. Initial stabilization was accomplished with nitric oxide and extracorporeal membrane oxygenation. The tricuspid valve repair surgery was successfully performed subsequently. TR resulting from papillary muscle rupture is a potentially lethal condition. Timely diagnosis and proper surgical treatment can be lifesaving.

摘要

因三尖瓣叶连枷样病变导致的非器质性三尖瓣反流(TR)是新生儿发绀的一种罕见病症。这种致命病症与围产期高死亡率相关。但是,有可行的外科修复方法可提高生存率。我们报告一例患有顽固性低氧血症的足月男婴病例。他因支撑三尖瓣前叶的乳头肌破裂而出现严重的三尖瓣关闭不全和瓣叶脱垂。出生后他立即出现严重发绀和呼吸窘迫。尽管进行了药物治疗,但肺血管阻力并未降低,心输出量持续较低。最初通过一氧化氮和体外膜肺氧合实现了病情稳定。随后成功进行了三尖瓣修复手术。乳头肌破裂导致的TR是一种潜在的致命病症。及时诊断和恰当的外科治疗可挽救生命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b9/4521114/48f9211dd68a/kcj-45-340-g001.jpg

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