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Protein‐losing enteropathy in an adult with non‐ischaemic cardiomyopathy: complete reversal by heart transplantation

机译:成人非缺血性心肌病的蛋白质丢失性肠病:通过心脏移植完全逆转

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摘要

Protein‐losing enteropathy (PLE) due to leakage of lymph into the gut sometimes occurs in young patients after Fontan palliation but is very rarely reported with other aetiologies of chronic heart failure (HF). PLE leads to severe hypoalbuminemia and immunodeficiency and is associated with poor prognosis. The mechanisms and the predispositions to PLE are poorly understood. Here, we report an adult patient with advanced HF due to non‐ischaemic non‐dilated hypocontractile cardiomyopathy who developed severe PLE, probably owing to increased ventricular stiffness and constraint by atypically placed epicardial electrode encircling both ventricles. Importantly, both PLE and immunodeficiency completely resolved after heart transplantation.
机译:在年轻患者中,Fontan缓解后,有时会因淋巴漏入肠道而导致蛋白质丢失性肠病(PLE),但很少有慢性心力衰竭(HF)的其他病因报道。 PLE导致严重的低白蛋白血症和免疫缺陷,并与不良预后相关。人们对PLE的机制和易感性知之甚少。在这里,我们报道了由于非缺血性非扩张性低收缩性心肌病而发展为重度PLE的一名成年患者,其发展为严重的PLE,这可能是由于心室僵硬度增加以及非典型心外膜电极包围两个心室所致。重要的是,心脏移植后,PLE和免疫缺陷均得到完全解决。

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