主动脉瓣和主动脉壁的巨大、侵袭性和破坏性 Abiotrophia Defectiva 心肌内膜炎。一例紧急但成功的儿童 Ross-Konno 手术病例报告

Cetera Vera, Cantinotti Massimiliano, Barberi Elisa, Pak Vitali
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摘要

缺损性阿米巴原虫(Abiotrophia defectiva)形成革兰氏阳性球菌,是正常口咽和胃肠道菌群的一部分,很少与儿童心内膜炎有关。其特殊的营养需求和亚急性临床过程可能会延误诊断和正确治疗,导致危及生命的后果。 我们报告了一例罕见的 3 岁儿童主动脉瓣和主动脉壁巨大破坏性 Abiotrophia Defectiva 感染性心内膜炎病例,该病例是先天性主动脉瓣狭窄手术瓣膜成形术后的随访病例。患儿到我院就诊时出现左侧偏瘫症状。经胸超声心动图显示,由于大面积植被延伸到主动脉壁直至主动脉弓,导致严重的主动脉瓣反流。血液培养结果显示,A. Defectiva呈阳性。患者最初接受抗生素保守治疗,但入院 10 天后,病情突然恶化,需要插管并进行紧急罗斯-康诺手术。尽管病情危重,手术风险很大,但患儿恢复良好,术后5周就出院回家了。 A. Defectiva IE 在儿童中非常罕见。自 1995 年以来,包括本病例在内,仅有 16 例儿童感染 A. Defectiva IE 的报道。与成人相比,这种病原体在儿童中的并发症发生率更高。我们的病例表明,使用抗生素的保守治疗策略很少能解决由变形杆菌引起的 IE。只要存在一个或多个手术指征,即使临床条件不允许且手术风险很高,也应考虑手术治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Huge, Invasive, and Destructive Abiotrophia Defectiva Endocarditis of the Aortic Valve and the Aortic Wall. A Case Report of an Emergency but Successful Ross-Konno Operation in a Child
Abiotrophia defectiva forms Gram-positive cocci, part of normal oropharyngeal and gastrointestinal flora and is rarely involved in endocarditis in children population. Its special nutritional requirements and subacute clinical course, may delay diagnosis and proper treatment, leading to life-threatening consequences. We report a rare case of huge and destructive Abiotrophia Defectiva infective endocarditis of the aortic valve and the aortic wall in a 3-years-old child, in follow-up after surgical valvuloplasty for congenital aortic stenosis. The child presented at our department with signs of left side hemiplegia. Transthoracic echocardiography showed severe aortic regurgitation due to large vegetation extending to the aortic wall up to the aortic arch. Blood cultures resulted positive for A. Defectiva. Initially treated conservatively with antibiotic therapy, but 10 days after admission, sudden clinical deterioration, required intubation and an emergency Ross-Konno operation. Despite the critical conditions and highly risky surgery, the child recovered well and was discharged home 5 weeks after the operation. A. Defectiva IE is rare in children. Since 1995, only sixteen cases of A. Defectiva IE have been reported in children, including our case. This pathogen has a higher rate of complications when affecting children rather than adult population. Our case demonstrates that conservative strategy with antibiotics is rarely resolutive in case of IE caused by A. Defectiva. Whenever one or more indications for surgery are present, surgical intervention should be always taken into consideration, even if clinical conditions are prohibitive and surgery is at very high risk.
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