壁性心内膜炎-默认

A. Patel, D. Kakooza, T. Kalk, N. Tsabedze
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引用次数: 0

摘要

我们报告一例33岁的女性患者,已知成人先天性心脏病,冠状动脉cameral瘘的形式,谁,在先前的表现,拒绝治疗,随后默认随访,但不幸的是发展了严重的和罕见的并发症。她表现出暂时性视力丧失和头痛等非特异性神经学症状。临床检查显示主动脉反流伴感染性心内膜炎的外周特征。经胸超声心动图证实了这一点,但除此之外,我们发现右心房后壁心内膜炎。最初的CT脑部扫描和眼科评估呈阴性,血液培养呈阳性,确认感染性心内膜炎,并被转至紧急心胸外科。不幸的是,她出现了进一步的并发症,颅内大出血,最终导致她死亡。这个病例说明了一个罕见的实体与灾难性的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mural endocarditis - by default
We report on a case of a 33-year-old female patient with known adult congenital heart disease in the form of a coronary cameral fistula who, on prior presentation, had refused treatment and subsequently defaulted follow-up, but unfortunately developed a serious and rare complication. She presented with non-specific neurological symptoms of transient visual loss and headaches. Clinical examination revealed aortic regurgitation with peripheral features of infective endocarditis. This was confirmed with transthoracic echocardiogram, but additionally, we found mural endocarditis of the right atrial posterior wall. An initial CT brain scan and ophthalmology assessments were negative, blood cultures were positive and confirmed infective endocarditis, and she was referred for urgent cardiothoracic surgery. Unfortunately, she had further complications with a large intracranial haemorrhage which ultimately led to her death. This case illustrates a rare entity with disastrous complications.
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