Asif Talal, Mohiuddin Amena, Hasan Badar, Masoud Amgad
Department of Internal Medicine, University of Missouri Kansas City (UMKC).
Cureus. 2017 Apr 19;9(4):e1176. doi: 10.7759/cureus.1176.
Spontaneous subarachnoid hemorrhage (SAH) as the presenting feature of infective endocarditis (IE) is rare. It has classically been described in association with the rupture of intracranial mycotic aneurysms (ICMA). Here we describe a very rare case of non-aneurysmal spontaneous SAH in a patient with IE. The patient originally presented with a headache and low-grade fever. Neuroimaging including computed tomography (CT) and magnetic resonance imaging (MRI) of the head revealed SAH. She was eventually diagnosed with streptococcus gallolyticus (formerly streptococcus bovis) IE. Through this case, we advocate consideration of the diagnosis of IE in patients with SAH so that there is timely recognition of this reversible but serious disease.
自发性蛛网膜下腔出血(SAH)作为感染性心内膜炎(IE)的首发症状较为罕见。传统上认为它与颅内真菌性动脉瘤(ICMA)破裂有关。在此,我们描述一例IE患者发生非动脉瘤性自发性SAH的极罕见病例。该患者最初表现为头痛和低热。包括头颅计算机断层扫描(CT)和磁共振成像(MRI)在内的神经影像学检查显示为SAH。她最终被诊断为解脲链球菌(以前称为牛链球菌)IE。通过这个病例,我们主张对SAH患者考虑IE的诊断,以便及时识别这种可逆但严重的疾病。