一名植入人工耳蜗的先天性耳聋患者因苏萨克综合征而死亡。

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
John E Richter, Katelyn S Rourk, Michael W Stewart, Mallory J Raymond
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引用次数: 0

摘要

目的报告一例致命的苏萨克综合征病例,患者先天性耳聋,植入人工耳蜗,有偏头痛病史:患者:33 岁男性,患有先天性听力损失、人工耳蜗植入术和慢性偏头痛,曾出现轻度亚急性听觉障碍和头痛,后发展为严重脑病:干预措施:植入非磁共振成像(MRI)兼容的人工耳蜗,然后进行磁共振成像、眼底镜检查,并服用免疫抑制药物:通过磁共振成像的特征性外观和半视网膜动脉闭塞的存在来确诊:经过数周的免疫抑制治疗后,患者死于原因不明的全脑缺血事件:对于已有感音神经性听力损失并植入人工耳蜗的患者来说,苏萨克综合征是一个诊断难题。在没有人工耳蜗植入失败的情况下出现听觉障碍,应进一步评估视觉障碍和脑病。应进行核磁共振成像和眼底镜检查,以发现该病的其他特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fatal Presentation of Susac Syndrome in a Congenitally Deaf Patient With a Cochlear Implant.

Objective: To report a fatal case of Susac syndrome in a congenitally deaf patient with a cochlear implant and a history of migraines, emphasizing the diagnostic challenges in patients with preexisting conditions.

Patient: A 33-year-old male with congenital hearing loss, a cochlear implant, and chronic migraines who presented with mild subacute auditory disturbance and headaches that later progressed to severe encephalopathy.

Intervention: Explantation of a non-magnetic resonance imaging (MRI) compatible cochlear implant followed by MRI, fundoscopy, and the administration of immunosuppressive medications.

Main outcome measures: Diagnosis was confirmed by characteristic MRI appearance and the presence of a hemi-retinal artery occlusion.

Results: After weeks of immunosuppressive treatment, the patient died of a global cerebral ischemic event of unknown origin.

Conclusions: For patients with preexisting sensorineural hearing loss and cochlear implants, Susac syndrome poses a diagnostic challenge. Auditory disturbances in the absence of cochlear implant failure should prompt further evaluation for visual disturbances and encephalopathy. MRI and fundoscopy should be performed to detect other features of the disease.

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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
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