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心内膜心肌纤维化:三尖瓣缺失及类Fontan循环。

Endomyocardial fibrosis: missing tricuspid valve and Fontan-like circulation.

作者信息

Shiraishi Yasuyuki, Kohno Takashi, Fujii-Nishimura Yoko, Shimoda Masayuki, Ikeda Yoshihiko, Nakajima Kazuaki, Nishiyama Takahiko, Nishiyama Nobuhiro, Murata Mitsushige, Maekawa Yuichiro, Sano Motoaki, Fukuda Keiichi

机构信息

Division of Cardiology, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

Department of Pathology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Heart Vessels. 2016 Sep;31(9):1579-82. doi: 10.1007/s00380-015-0792-8. Epub 2016 Jan 8.

Abstract

Endomyocardial fibrosis (EMF) is a progressive type of obliterative/restrictive cardiomyopathy characterized by fibrosis of the apical endomyocardium of the ventricles. Although the prognosis of EMF patients is poor in tropical regions, the exact clinical course and pathogenesis of patients with EMF are not known. Here, we report the rare case with EMF in the seventh decade, who showed the disappearance of papillary muscles, chordae tendineae, and part of the tricuspid valves due to massive right ventricular thrombus. Because of those unusual findings of the isolated RV involvement, we observed continuous forward pulmonary artery flow, as occurring in a Fontan circulation.

摘要

心内膜心肌纤维化(EMF)是一种进行性闭塞性/限制性心肌病,其特征是心室心尖部心内膜纤维化。尽管在热带地区EMF患者的预后较差,但EMF患者的确切临床病程和发病机制尚不清楚。在此,我们报告了一例罕见的70岁EMF病例,该患者因大量右心室血栓导致乳头肌、腱索和部分三尖瓣消失。由于孤立性右心室受累的这些异常表现,我们观察到持续的肺动脉前向血流,如同在Fontan循环中出现的那样。

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