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岩骨段颈内动脉误诊为动脉瘤:一例报告。

A misdiagnosed aneurysm of the petrous internal carotid artery: A case report.

作者信息

Alouda Nada, Alshammari Nouf H, Alomar Khalid Suwayyid, Shami Ibrahim, Alobaid Abdullah Omar

机构信息

Department of Otolaryngology-Head & Neck Surgery, King Saud University Medical City, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Department of Otolaryngology-Head & Neck Surgery, King Fahad Medical City, Riyadh, Saudi Arabia.

出版信息

Int J Surg Case Rep. 2023 Sep;110:108671. doi: 10.1016/j.ijscr.2023.108671. Epub 2023 Aug 24.

Abstract

INTRODUCTION

An aneurysm is characterized by the weakening of the arterial wall, which leads to a bulge that can be filled with blood. Aneurysms of the petrous portion of the internal carotid artery are rare and predominantly detected incidentally. This is a report of multiple misdiagnoses of an aneurysm of the petrous segment of the internal carotid artery (ICA) that highlights its imaging-based diagnosis and risk of mortality.

PRESENTATION OF CASE

A 60-year-old woman with chronic kidney disease and a history of stroke presented with left ear discharge, decreased hearing, and non-pulsatile tinnitus that had persisted for four months. Clinical examination showed wet tympanic membrane perforation, and imaging revealed an ill-defined infiltrative mass involving the left petrous apex initially misdiagnosed as glomus jugulare. Diagnostic computed tomography (CT) angiography revealed a left aneurysm in the petrous part of the ICA, which was successfully treated with interventional radiology. Follow-up was planned for infectious diseases and internal medicine, but she was lost to follow-up by the otolaryngology department.

DISCUSSION

Aneurysms in the petrous portion of the ICA are rare and usually asymptomatic. However, their clinical manifestations vary, and they have various differential diagnoses. CT and magnetic resonance imaging are essential for diagnosis, and CT angiography is the gold standard.

CONCLUSION

Diagnosing petrous ICA aneurysms requires a high level of suspicion and CT angiography. Their clinical presentations vary from asymptomatic to severe. Case-specific management and endovascular treatment yield positive neurological outcomes.

摘要

引言

动脉瘤的特征是动脉壁薄弱,导致可充满血液的膨出。颈内动脉岩骨段动脉瘤罕见,主要为偶然发现。本文报告一例颈内动脉岩骨段动脉瘤多次误诊的病例,强调其基于影像学的诊断及死亡风险。

病例介绍

一名60岁女性,有慢性肾病和中风病史,出现左耳流脓、听力下降及非搏动性耳鸣4个月。临床检查显示鼓膜穿孔伴中耳积液,影像学检查最初发现左侧岩尖有边界不清的浸润性肿块,误诊为颈静脉球瘤。诊断性计算机断层扫描(CT)血管造影显示颈内动脉岩骨段左侧动脉瘤,经介入放射学成功治疗。计划对其进行传染病及内科随访,但耳鼻喉科失去了对她的随访。

讨论

颈内动脉岩骨段动脉瘤罕见,通常无症状。然而,其临床表现各异,有多种鉴别诊断。CT和磁共振成像对诊断至关重要,CT血管造影是金标准。

结论

诊断颈内动脉岩骨段动脉瘤需要高度怀疑并采用CT血管造影。其临床表现从无症状到严重不等。针对具体病例的管理和血管内治疗可产生积极的神经学结果。

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