Boukobza Monique, Duval Xavier, Laissy Jean-Pierre
Department of Radiology, Assistance Publique-Hôpitaux de Paris, Bichat University Hospital, 46 rue Henri Huchard, 75018 Paris, France.
Department of Infectious Diseases, Assistance Publique-Hôpitaux de Paris, Bichat University Hospital, Paris, France; INSERM Clinical Investigation Center 007, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, France.
J Clin Neurosci. 2019 Apr;62:222-225. doi: 10.1016/j.jocn.2018.12.035. Epub 2019 Jan 9.
Acute subdural hematoma (ASDH) revealing mycotic aneurysm (MA) is an exceptional occurrence. We report 2 cases of MA-related pure ASDH in the course of infective endocarditis (IE) without history of head trauma, hypertension or coagulopathy. Case 1: A 54-year-old man presented with a 10-day history of headache, fever. At admission neurologic examination and Brain-CT were normal. Blood cultures showed Streptococcus bovis. MRI 5 days later revealed ischemic spots and minime ASDH over the right convexity. Cerebral angiography, revealed a 3 mm saccular aneurysm at the bifurcation of a distal branch of the right posterior cerebral artery (PCA). Case 2: A 42-year-old man presented with a 8-day history of fever, and worsening headache. Mitral regurgitation was evidenced. A methicillin-sensitive staphylococcus aureus left-sided IE was diagnosed. Pre- and post-contrast Brain-CT were normal. He presented 15 days later a secondarily generalized status epilepticus. Brain CT showed an ASDH over the convexity with falco-tentorial extension, midline shift and temporal herniation. It was removed in emergency. Cerebral angiography revealed a MA of a peripheral branch of the left PCA. The 2 patients were successfully treated by endovascular glue embolization and recovered without complications. Even rare, ruptured MA should be considered as a cause of pure ASDH of unknown origin. As MA can be missed on CT- and MR-Angiography because of mass effect, cerebral angiography may be mandatory.
急性硬膜下血肿(ASDH)合并霉菌性动脉瘤(MA)极为罕见。我们报告2例在感染性心内膜炎(IE)病程中出现的与MA相关的单纯ASDH病例,患者无头部外伤、高血压或凝血功能障碍病史。病例1:一名54岁男性,有10天头痛、发热病史。入院时神经系统检查和脑部CT均正常。血培养显示牛链球菌。5天后的MRI显示右侧脑凸面有缺血灶和微小ASDH。脑血管造影显示右大脑后动脉(PCA)远端分支分叉处有一个3毫米的囊状动脉瘤。病例2:一名42岁男性,有8天发热及头痛加重病史。证实有二尖瓣反流。诊断为左侧甲氧西林敏感金黄色葡萄球菌性IE。增强前后脑部CT均正常。15天后他出现继发性全身性癫痫持续状态。脑部CT显示脑凸面有ASDH,延伸至小脑幕,中线移位和颞叶疝。急诊行血肿清除术。脑血管造影显示左PCA外周分支有一个MA。2例患者均通过血管内胶水栓塞成功治疗,康复且无并发症。即使MA破裂罕见,但仍应考虑其为不明原因单纯ASDH的病因之一。由于占位效应,MA在CT血管造影和MR血管造影上可能漏诊,因此脑血管造影可能是必要的。