Daoud Hussein, Abugroun Ashraf, Olanipekun Olalekan, Garrison Daniel
Department of Internal Medicine, Advocate Illinois Masonic Medical Center, 836 W Wellington Ave., Chicago, IL, 60657, USA.
IDCases. 2019 May 17;17:e00561. doi: 10.1016/j.idcr.2019.e00561. eCollection 2019.
is a rare cause of infective endocarditis that was first described in 1940 by Khairat et al. and is now classified under the HACEK group of bacteria ( spp. spp.. There is limited literature describing the extracardiac complications of infective endocarditis caused by this organism. We report a case of a 53-year-old male with no significant past medical history who developed acute infective endocarditis complicated by a brain abscess caused by . The patient underwent aspiration of the abscess and treated with a long course of intravenous antimicrobials. This case represents a rare complication of infective endocarditis caused by A. aphrophilus and to the best of our knowledge, is the second reported case in the literature describing such a complication in a previously healthy patient. Although neurological sequela is associated with higher mortality and may be the presenting symptom of infective endocarditis, it may also be clinically silent - only detected upon imaging.
是感染性心内膜炎的罕见病因,1940年由海拉特等人首次描述,现归类于HACEK菌群( 菌属、 菌属)。关于该病原体引起的感染性心内膜炎的心外并发症的文献有限。我们报告一例53岁男性,既往无重大病史,发生急性感染性心内膜炎,并伴有由 引起的脑脓肿。患者接受了脓肿穿刺,并接受了长期静脉抗菌治疗。该病例代表了由嗜沫嗜血杆菌引起的感染性心内膜炎的罕见并发症,据我们所知,是文献中报道的第二例描述此前健康患者出现此类并发症的病例。尽管神经后遗症与较高的死亡率相关,可能是感染性心内膜炎的首发症状,但也可能在临床上无症状——仅在影像学检查时发现。