Management of Massive Iatrogenic Temporal Lobe Meningoencephalocele and Bacterial Meningitis Following Pediatric Cochlear Implant Surgery.

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Otology & Neurotology Pub Date : 2025-01-01 Epub Date: 2024-11-06 DOI:10.1097/MAO.0000000000004358
Samantha M Shave, Camelia N Saber, Abel P David, Daniel J Lee
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Abstract

Objective: To review the management of meningitis, large lateral skull base defect, and meningoencephalocele following pediatric cochlear implant (CI) surgery.

Study design: Case report.

Methods: Patient demographics, medical and surgical history, computed tomography (CT).

Results: An 8-year-old male with congenital severe to profound sensorineural hearing loss underwent uncomplicated right CI surgery at 18 months of age. He returned to his home country and received a bilateral sequential left ear CI at age 2. Five years following his second CI surgery, he presented to his local emergency room with worsening fever, headache, back pain, and vomiting. Lumbar puncture confirmed bacterial meningitis, and he was managed with intravenous antibiotics. The hospital course was complicated by a right-sided facial nerve paresis, prompting a temporal bone CT. Imaging demonstrated a tegmen defect measuring 15 mm × 10 mm with soft tissue opacification involving the entire mastoid and CI harness. He was then referred by family back to our institution. Intraoperatively, we identified a massive temporal lobe meningoencephalocele involving the entire mastoid cavity and engulfing the entire proximal electrode harness. Following middle cranial fossa craniotomy and revision mastoidectomy, proximal and distal array were separated, encephalocele transected, and remaining temporal lobe reduced. The lateral skull base was reconstructed with calvarial bone, temporalis fascia, and bovine collagen graft. The remnant electrode array was removed, a new CI receiver stimulator was fixed postero-superiorly to the cranial defect, and a new multichannel array inserted. A titanium cranioplasty completed the repair. A lumbar drain was placed for 3 days. Recovery and CI activation occurred uneventfully.

Conclusion: Risk of encephalocele and meningitis underscores the importance of early identification, adequate repair, and long-term radiologic follow-up of iatrogenic tegmen defects during pediatric CI surgery.

小儿人工耳蜗手术后大面积颞叶脑膜脑炎和细菌性脑膜炎的处理。
研究目的回顾小儿人工耳蜗(CI)手术后脑膜炎、大侧颅底缺损和脑膜脑炎的处理方法:研究设计:病例报告:研究设计:病例报告。方法:患者人口统计学、病史和手术史、计算机断层扫描(CT):一名患有先天性重度至极重度感音神经性听力损失的 8 岁男童在 18 个月大时接受了右侧人工耳蜗手术,手术过程并不复杂。他回到祖国后,在 2 岁时接受了双侧顺序左耳 CI。第二次 CI 手术后五年,他因发烧、头痛、背痛和呕吐症状加重而到当地急诊室就诊。腰椎穿刺证实他患有细菌性脑膜炎,并接受了静脉抗生素治疗。右侧面神经瘫痪使住院过程变得复杂,促使他接受了颞骨 CT 检查。造影显示他的颞骨有一个 15 毫米 × 10 毫米的缺损,整个乳突和 CI 线束软组织不透明。随后,患者家属将其转诊至我院。术中,我们发现了一个巨大的颞叶脑膜脑瘤,涉及整个乳突腔,并吞噬了整个近端电极束。在进行中颅窝开颅手术和改良乳突切除术后,分离了近端和远端阵列,横断了脑瘤,缩小了剩余的颞叶。用犊骨、颞筋膜和牛胶原移植重建了侧颅底。移除残余电极阵列,在颅骨缺损后上方固定一个新的 CI 接收刺激器,并插入一个新的多通道阵列。钛合金颅骨成形术完成了修复。腰部引流管放置了 3 天。术后恢复和 CI 激活都很顺利:结论:脑疝和脑膜炎的风险凸显了在小儿 CI 手术中早期识别、充分修复和长期放射学随访先天性颅骨缺损的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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