Middle Ear Cholesteatoma Complicated By Lemierre's Syndrome: A Case Report and Literature Review.

Xiaoyu Zhu, Hua Deng, Ming Yu, Shasha Yang, Qingxin Cao, Chengyan Zhao, Ying Wang, Jiexi Jiang, Yusui Zhang
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Abstract

Septic thrombophlebitis of the internal jugular vein (IJV), known as Lemierre's syndrome, is a rare complication secondary to infections in the head and neck. Cholesteatoma of the middle ear complicated with Lemierre's syndrome is rarely observed in clinical practice. Currently, the treatment controversy centers on whether anticoagulation therapy is necessary for IJV and distant metastatic emboli induced by Lemierre's syndrome. A 46-year-old female patient with middle ear cholesteatoma underwent modified radical mastoidectomy and tympanoplasty surgery and complicated with Lemierre's syndrome, presenting with intermittent high fever, chills, headache, and left lateral neck pain. Computed tomography (CT) revealed thrombosis and internal gas in the left IJV, while blood culture and blood pathogenic microorganism metagenomic detection were negative. We administered sodium ceftriaxone (1 g every 12 hours) for 3 days. According to the secretion culture results showing 90% Actinomyces europaeus and 10% Corynebacterium without mycolic acid, penicillin (2.4 million IU) was added intravenously every 6 hours. The patient's infection worsened on the first day after surgery. We adjusted to upgrade anti-infection vancomycin 1 g every 12 hours, combined with meropenem (1 g every 8 hours) and metronidazole (0.5 g) every 8 hours for 4 weeks, and subcutaneous injection of enoxaparin 0.4 mL every 12 hours for 1 week, then adjusted to rivaroxaban tablets (15 mg bid). Amoxicillin-clavulanate for 2 weeks and rivaroxaban 10 mg were administered orally for 3 months after discharge. A follow-up neck CT scan with intravenous contrast suggested that the gas in the left IJV had disappeared, but the thrombus persisted. During the 3 month follow-up, the patient's vital signs, blood routine, and D-dimer levels were within the normal range. The surgical area healed well, and the patient reported no discomfort. Lemierre's syndrome represents a potentially-fatal complication that results in considerable mortality and must be identified early and aggressively treated.

中耳胆脂瘤合并By Lemierre综合征1例报告并文献复习。
颈内静脉化脓性血栓性静脉炎(IJV),又称Lemierre综合征,是一种罕见的头颈部感染继发并发症。中耳胆脂瘤合并Lemierre综合征在临床上是罕见的。目前,治疗争议主要集中在Lemierre综合征引起的IJV和远处转移性栓塞是否需要抗凝治疗。46岁女性中耳胆脂瘤患者行改良根治性乳突切除术和鼓室成形术,并发Lemierre综合征,表现为间歇性高热、寒战、头痛和左颈外侧疼痛。CT示左侧IJV血栓形成及内部气体形成,血培养及血液病原微生物宏基因组检测均为阴性。给药头孢曲松钠(每12小时1 g),连续3天。根据分泌物培养结果显示90%的europaeus放线菌和10%的棒状杆菌不含霉菌酸,每6小时静脉滴注青霉素240万IU。术后第一天患者感染加重。我们调整抗感染万古霉素每12小时升级1 g,联合美罗培南(每8小时1 g)、甲硝唑(每8小时0.5 g),持续4周,依诺肝素每12小时皮下注射0.4 mL,持续1周,然后调整为利伐沙班片(bid 15mg)。出院后口服阿莫西林-克拉维酸2周,利伐沙班10 mg,持续3个月。随后的颈部CT扫描和静脉造影剂显示左侧IJV的气体已经消失,但血栓仍然存在。随访3个月,患者生命体征、血常规、d -二聚体水平均在正常范围内。手术区域愈合良好,患者报告无不适。Lemierre综合征是一种潜在的致命并发症,可导致相当大的死亡率,必须及早发现并积极治疗。
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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