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硬脑膜下脓胸——慢性中耳炎的罕见并发症:一例报告。

Subdural empyema-a rare complication of chronic otitis media: a case report.

机构信息

Barentu Military Hospital, Barentu, Eritrea.

Mendefera Zonal Referral Hospital, Mendefera, Eritrea.

出版信息

J Med Case Rep. 2024 Aug 3;18(1):351. doi: 10.1186/s13256-024-04671-4.

Abstract

BACKGROUND

Subdural empyema is an extremely rare and fatal intracranial complication of chronic otitis media. Due to its rarity and vague symptoms, it is often diagnosed late if not completely missed; specially in developing countries where the diagnostic modalities are hardly available or accessible. To the best knowledge of the authors, this is a preliminary reported case of subdural empyema as a complication of chronic otitis media in Eritrea. It aims to provide vital information on the clinical presentation, preferred diagnostic modalities, and the proper management of such cases.

CASE REPORT

An 8 years old female patient from the Rashaida ethnic group presented with fever, right ear purulent discharge, right post-auricular swelling, and altered mental status. Prior to her admission, she had history of recurrent purulent discharge from her right ear for almost 2 years, and had been diagnosed with chronic otitis media. Upon admission her GCS was 13/15 which later on deteriorated to be 3/15 on day 3. MRI was done and showed a right fronto-tempo-parietal subdural empyema with mass effect, shifting the midline to the left. She was immediately started on empirical broad-spectrum antibiotics. After the diagnosis was made, craniotomy was done, and 30 ml of pus was removed from the subdural space. Culture and sensitivity of the pus obtained intraoperatively was done but produced no yield. Hence, she was continued on the empirically started antibiotics. The patient's condition was well improved by post-operative day 4.

CONCLUSION

It is important to have a high index of suspicion of intracranial complications in patients with history of chronic otitis media or other otologic complaints, who present with neurologic manifestations. Subdural empyema still being uncommon even among the intracranial complications of COM, it is often missed. Hence, timely diagnosis with MRI, immediate surgical evacuation of the empyema along with the prolonged administration of broad-spectrum antibiotics is highly recommended.

摘要

背景

硬脑膜下脓胸是慢性中耳炎极为罕见且致命的颅内并发症。由于其罕见性和模糊的症状,如果不被完全忽视,通常会被误诊或漏诊;特别是在诊断手段难以获得或无法获得的发展中国家。据作者所知,这是厄立特里亚首例慢性中耳炎并发硬脑膜下脓胸的初步报告病例。旨在提供有关此类病例临床表现、首选诊断方式和适当治疗的重要信息。

病例报告

一名 8 岁女性患者,属于拉沙伊达族,表现为发热、右耳脓性分泌物、耳后肿胀和精神状态改变。在入院前,她的右耳反复发作脓性分泌物已有近 2 年,被诊断为慢性中耳炎。入院时,她的 GCS 评分为 13/15,第 3 天恶化至 3/15。进行 MRI 检查,显示右额颞顶硬脑膜下积脓伴占位效应,中线向左移位。立即开始经验性广谱抗生素治疗。诊断后,立即行开颅术,从硬脑膜下腔中取出 30ml 脓液。对术中获得的脓液进行了培养和药敏试验,但未得到结果。因此,继续使用经验性开始的抗生素。术后第 4 天,患者病情明显好转。

结论

对于有慢性中耳炎或其他耳科症状病史、出现神经系统表现的患者,应高度怀疑颅内并发症。即使在慢性中耳炎的颅内并发症中,硬脑膜下脓胸仍然不常见,也常常被忽视。因此,强烈建议及时进行 MRI 诊断,立即进行脓胸手术清除,并长期使用广谱抗生素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/012d/11297699/470645d0cfe0/13256_2024_4671_Fig1_HTML.jpg

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