Gilderman Gina S, Morsy Mahmoud, Antony Nishaal
Department of Medicine, Burrell College of Osteopathic Medicine, New Mexico, USA.
Department of Medicine, Mayo Clinic, Arizona, USA.
Cureus. 2023 Mar 10;15(3):e35977. doi: 10.7759/cureus.35977. eCollection 2023 Mar.
species are a rare cause of infective endocarditis (IE). We describe a case of native valve endocarditis caused by in a 38-year-old Hispanic male with no apparent environmental exposures or risk factors for IE. Transesophageal echocardiography revealed severe mitral regurgitation, prompting emergent replacement of the valve. were isolated from the tissue culture of the mitral valve. MRI of the brain also demonstrated innumerable micronodular intra-axial lesions throughout the brain, consistent with disseminated nocardiosis. The patient was treated with intravenous trimethoprim/sulfamethoxazole, meropenem, and amikacin for a six-week course, followed by oral trimethoprim/sulfamethoxazole and minocycline for 12 months. Follow-up after 18 months revealed no evidence of relapse. Although several cases of endocarditis due to have been reported in immunocompromised hosts, to the best of our knowledge we believe the present case is the first to describe native valve endocarditis by in an immunocompetent host with no apparent risk factors for IE.
某些菌种是感染性心内膜炎(IE)的罕见病因。我们描述了一例由[菌种名称未给出]引起的自体瓣膜心内膜炎病例,患者为一名38岁的西班牙裔男性,无明显的环境暴露因素或IE危险因素。经食管超声心动图显示严重二尖瓣反流,促使紧急进行瓣膜置换。从二尖瓣组织培养中分离出了[菌种名称未给出]。脑部MRI还显示全脑有无数微小结节性轴内病变,符合播散性诺卡菌病。患者接受了为期六周的静脉注射甲氧苄啶/磺胺甲恶唑、美罗培南和阿米卡星治疗,随后口服甲氧苄啶/磺胺甲恶唑和米诺环素治疗12个月。18个月后的随访显示无复发迹象。尽管在免疫功能低下宿主中已有数例由[菌种名称未给出]引起的心内膜炎报道,但据我们所知,我们认为本病例是首例描述在无明显IE危险因素的免疫功能正常宿主中由[菌种名称未给出]引起的自体瓣膜心内膜炎。