[壁内主动脉血肿致奥尔特纳综合征：一例报告]

[Ortner's syndrome caused by intramural aortic hematoma: a case report].

作者信息

Jin Yingyu, Sun Xiaohui, Liu Yang, Wang Yanfang, Xu Yinwei, Jia Jianping

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Jan 5;35(1):74-76. doi: 10.13201/j.issn.2096-7993.2021.01.019.

DOI:10.13201/j.issn.2096-7993.2021.01.019

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10128530/

Abstract

The clinical manifestations were hoarseness, and no sore throat, fever, dyspnea and dysphagia were found. The patient was in good health and had no history of cardiovascular disease, throat disease, diabetes, asthma, tumor, etc. The left vocal cord paralysis was seen by electronic laryngoscope, and aortic intramural hematoma was found by chest CT examination. In addition, we combined MIMICS digital 3D reconstruction technology to further clarify the lesion. After a series of physical examinations and related examinations, the patient was finally diagnosed as Ortner's syndrome caused by a rare cause of aortic intramural hematoma.

摘要

临床表现为声音嘶哑，未发现咽痛、发热、呼吸困难及吞咽困难。患者身体健康，无心血管疾病、咽喉疾病、糖尿病、哮喘、肿瘤等病史。电子喉镜检查可见左侧声带麻痹，胸部CT检查发现主动脉壁内血肿。此外，我们结合MIMICS数字3D重建技术进一步明确病变情况。经过一系列体格检查及相关检查，患者最终被诊断为由罕见病因主动脉壁内血肿引起的奥纳综合征。

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本文引用的文献

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A fatal case of Ortner's syndrome and dysphagia aortica secondary to rapidly expanding mycotic thoracic aortic aneurysm in a chronic kidney disease patient.一名慢性肾病患者因快速扩张的霉菌性胸主动脉瘤继发奥尔特纳综合征和主动脉性吞咽困难的致死病例。

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