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真菌性颅内动脉瘤破裂在感染性心内膜炎中表现为单纯急性硬膜下血肿。2例报告并文献复习。

Mycotic intracranial aneurysms rupture presenting as pure acute subdural hematoma in infectious endocarditis. Report of 2 cases and review of the literature.

作者信息

Boukobza Monique, Duval Xavier, Laissy Jean-Pierre

机构信息

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.

出版信息

J Clin Neurosci. 2019 Apr;62:222-225. doi: 10.1016/j.jocn.2018.12.035. Epub 2019 Jan 9.

DOI:10.1016/j.jocn.2018.12.035
PMID:30638783
Abstract

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.

摘要

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。

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