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揭示罕见病例:勒米尔综合征的非典型表现

Unmasking Rarity: An Atypical Presentation of Lemierre's Syndrome.

作者信息

Abdela Hayatu Awel, Woyimo Tamirat Godebo, Muktar Kumel Nur, Geremew Nahom Bitew, Abdulmalik Germen Temam, Weyeyso Feven Tadiwos, Lamessa Adugna

机构信息

Department of Internal Medicine Wolkite University Wolkite Ethiopia.

Department of Radiology Wolkite University Wolkite Ethiopia.

出版信息

Clin Case Rep. 2025 Sep 3;13(9):e70844. doi: 10.1002/ccr3.70844. eCollection 2025 Sep.

Abstract

Lemierre's syndrome (LS), otherwise known as postanginal sepsis, is a frequently overlooked condition characterized by septic thrombophlebitis of the internal jugular vein (IJV), usually caused by oropharyngeal infection. However, ear space (otogenic) infections are one of the atypical causes of LS and have been rarely reported. We present a case of a male in his 20s with a history of recurrent acute otitis media (RAOM) who presented with purulent ear discharge, fever, neck pain, and swelling for a week. Blood tests showed a raised white blood cell count with a left shift and increased inflammatory markers. Ear discharge and blood cultures were negative. A contrast-enhanced computed tomography (CT) scan of the head and neck revealed thrombosis of the IJV and opacification of the mastoid air space. The patient was diagnosed with otogenic LS and recurrent acute otitis media and responded well to empiric broad-spectrum antibiotics and supportive care. Anticoagulation therapy was not considered due to the lack of consensus on its effectiveness. After three months of follow-up, symptoms resolved, and venous Doppler ultrasound showed IJV recanalization. This case highlights a rare association and emphasizes the need for timely diagnosis and intervention. Therefore, due to the rare occurrence of the disease, heightened clinical vigilance is needed to avoid the adverse consequences of delayed diagnosis.

摘要

勒米尔综合征(LS),又称咽后败血症,是一种常被忽视的病症,其特征为颈内静脉(IJV)发生脓毒性血栓性静脉炎,通常由口咽感染引起。然而,耳部间隙(耳源性)感染是LS的非典型病因之一,且鲜有报道。我们报告一例20多岁男性病例,有复发性急性中耳炎(RAOM)病史,出现脓性耳漏、发热、颈部疼痛和肿胀一周。血液检查显示白细胞计数升高伴核左移,炎症标志物增加。耳漏和血培养均为阴性。头颈部增强计算机断层扫描(CT)显示颈内静脉血栓形成及乳突气房混浊。该患者被诊断为耳源性LS和复发性急性中耳炎,经验性使用广谱抗生素和支持治疗后反应良好。由于对其有效性缺乏共识,未考虑抗凝治疗。经过三个月的随访,症状缓解,静脉多普勒超声显示颈内静脉再通。本病例突出了一种罕见的关联,并强调了及时诊断和干预的必要性。因此,由于该疾病罕见,需要提高临床警惕性以避免延迟诊断的不良后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12be/12408373/315f01445ace/CCR3-13-e70844-g002.jpg

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