经皮腔内血管成形术及支架置入术治疗侵袭性蝶窦曲霉病继发的进行性颅内颈动脉狭窄1例。

Eisaku Terada, Takeo Nishida, Yuya Fujita, Yohei Maeda, Masaki Hayama, Masatoshi Takagaki, Hajime Nakamura, Satoru Oshino, Youichi Saitoh, Haruhiko Kishima
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引用次数: 0

摘要

我们报告一例侵袭性蝶窦曲霉病伴进行性颈内动脉(ICA)狭窄和对侧颈动脉闭塞,经皮腔内血管成形术和支架置入术(PTAS)成功治疗。一位70岁男性,表现为右侧视力障碍,上睑下垂和左偏瘫。头部磁共振成像显示蝶窦内占位性病变伴双侧海绵窦浸润,右侧ICA闭塞,累及右脑半球多发分水岭性脑梗死。根据经鼻活检结果诊断为侵袭性鼻窦曲霉病。尽管使用伏立康唑进行了强化抗真菌治疗,但快速进展的曲霉病导致左侧ICA出现新的狭窄病变,增加了双侧脑灌注不足的风险。我们成功地实施了PTAS来预防严重的缺血事件。经伏立康唑治疗,曲霉病得到控制,出院。他表现出良好的结果,在3年的随访中观察到一个专利左ICA。PTAS在ICA狭窄和侵袭性鼻窦曲霉病患者中是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Percutaneous Transluminal Angioplasty and Stenting for Progressive Intracranial Carotid Artery Stenosis Secondary to Invasive Sphenoid Sinus Aspergillosis: A Case Report.

Percutaneous Transluminal Angioplasty and Stenting for Progressive Intracranial Carotid Artery Stenosis Secondary to Invasive Sphenoid Sinus Aspergillosis: A Case Report.

Percutaneous Transluminal Angioplasty and Stenting for Progressive Intracranial Carotid Artery Stenosis Secondary to Invasive Sphenoid Sinus Aspergillosis: A Case Report.

Percutaneous Transluminal Angioplasty and Stenting for Progressive Intracranial Carotid Artery Stenosis Secondary to Invasive Sphenoid Sinus Aspergillosis: A Case Report.

We report a case of invasive sphenoid sinus aspergillosis with progressive internal carotid artery (ICA) stenosis and contralateral carotid occlusion that was successfully treated with percutaneous transluminal angioplasty and stenting (PTAS). A 70-year-old man presented with right-sided visual disturbance, ptosis, and left hemiparesis. Magnetic resonance imaging of the head revealed a space-occupying lesion within the sphenoid sinus with infiltration of the bilateral cavernous sinuses, right ICA occlusion, and multiple watershed cerebral infarcts involving the right cerebral hemisphere. The patient was diagnosed with invasive sinus aspergillosis based on transnasal biopsy findings. Despite intensive antifungal therapy using voriconazole, rapidly progressive aspergillosis led to a new stenotic lesion in the left ICA, which increased the risk of bilateral cerebral hypoperfusion. We performed successful PTAS to prevent critical ischemic events. Finally, aspergillosis was controlled with voriconazole treatment, and the patient was discharged. He showed a favorable outcome, with a patent left ICA observed at a 3-year follow-up. PTAS may be feasible in patients with ICA stenosis and invasive sinus aspergillosis.

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