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Case Report: Carotid–cavernous fistula due to aneurysmal rupture in a case of aortoaortitis with bilateral giant internal carotid artery aneurysms

机译:病例报告:主动脉炎伴双侧巨大颈内动脉瘤的主动脉炎引起的颈动脉海绵窦瘘

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摘要

Takayasu aortoarteritis (TA) rarely affects the nervous system, but when it does, it usually manifests as cerebral ischemia or stroke. These strokes have mainly been attributed to stenotic extracranial vessels. Stenoses of intracranial vessels, although rare in TA, can occur due to either embolization into the vessel or because of the vasculitic process itself. Intracranial aneurysms are very rare in patients with TA. Bilateral cavernous internal carotid artery (ICA) aneurysms are rarer. They have been reported following radiation therapy and in association with fibromuscular dysplasia and juvenile Paget disease. Bilateral mycotic intracavernous aneurysms also occur. Bilateral giant cavernous ICA aneurysms with carotid-cavernous fistula (CCF) consequent to rupture into the cavernous sinus in a case of TA are extremely unusual. We report a case that fulfilled both American College of Rheumatology and European League against Rheumatology criteria for TA. The patient had bilateral cavernous sinus giant aneurysms and CCF because the right-sided aneurysm had ruptured and was leaking into the cavernous sinus.
机译:Takayasu主动脉炎(TA)很少会影响神经系统,但是当它发生时,通常表现为脑缺血或中风。这些中风主要归因于狭窄的颅外血管。颅内血管狭窄虽然在TA中不多见,但可能是由于栓塞入血管或血管本身引起的。 TA患者颅内动脉瘤非常罕见。双侧海绵状颈内动脉(ICA)动脉瘤较为罕见。据报道,它们在放射治疗后并伴有纤维肌发育不良和少年Paget病。双侧霉菌性海绵体内动脉瘤也发生。在TA病例中,双侧巨大海绵状ICA动脉瘤伴颈动脉海绵窦瘘(CCF)破裂成海绵窦非常罕见。我们报告了一个案例,该案例符合美国风湿病学院和欧洲风湿病联盟针对TA的标准。该患者患有双侧海绵窦巨大动脉瘤和CCF,因为右侧动脉瘤破裂并渗入海绵窦。

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