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由于动脉导管宫内闭塞继发腱索断裂导致的先天性三尖瓣关闭不全。

Congenital tricuspid insufficiency due to rupture of chordae tendinea secondary to intrauterine obliteration of ductus arteriosus.

作者信息

Sari Gizem, Oteyaka Emre, Kuguoglu Okan Eren, Basunlu Mehmet Turan, Karakurt Yakup, Yozgat Yilmaz, Demirel Gamze, Ugurlucan Murat, Tastekin Ayhan, Turkoglu Halil

机构信息

Istanbul Medipol University Faculty of Medicine, Department of Pediatric Cardiology, Turkey.

Istanbul Medipol University Faculty of Medicine, Department of Cardiovascular Surgery, Turkey.

出版信息

Cardiol Young. 2023 Jan;33(1):149-152. doi: 10.1017/S1047951122001482. Epub 2022 May 12.

Abstract

Congenital rupture of tricuspid chordae tendinea leading to severe tricuspid insufficiency is an extremely rare pathology associated with signs and symptoms of congestive heart failure presenting at birth. If the diagnosis and treatment of this pathology are not made early in life fetal demise may become inevitable.We herein present a neonate with central cyanosis and congestive heart failure due to rupture of an anterior leaflet chordae resulting in severe insufficiency of the tricuspid valve who was treated with appropriate surgery.

摘要

先天性三尖瓣腱索破裂导致严重三尖瓣关闭不全是一种极其罕见的病理情况,与出生时出现的充血性心力衰竭的体征和症状相关。如果在生命早期未对这种病理情况进行诊断和治疗,胎儿死亡可能不可避免。我们在此报告一名新生儿,因前叶腱索破裂导致三尖瓣严重关闭不全,出现中心性发绀和充血性心力衰竭,接受了适当的手术治疗。

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