与2019冠状病毒病(COVID - 19)感染相关的致命性侵袭性肺曲霉病

S. Katta, M. Khoshnevis
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引用次数: 0

摘要

曲霉是一种普遍存在的真菌,可引起肺部多种临床综合征。曲霉引起的气道和实质疾病的类型和严重程度受患者免疫状况和既往肺部疾病的影响。人们越来越担心2019冠状病毒病(COVID-19)患者可能有发生侵袭性肺曲霉病合并感染的风险,特别是在免疫调节单克隆抗体的情况下。我们报告一例假膜曲菌性气管支气管炎合并COVID-19肺炎。59岁女性,既往有甲氨蝶呤所致药物性间质性肺疾病、类风湿关节炎病史,因呼吸困难和低氧性呼吸衰竭入住重症监护室。她最近被诊断患有COVID-19肺炎,接受了瑞德西韦和大剂量全身皮质类固醇治疗14天。一周后因呼吸短促再次入院,需要高流量鼻插管。体温38.2°,血压110/80 mmHg,心率90 bpm,呼吸频率30次/min。胸部听诊对弥漫性双侧吸气性粗裂有重要意义。她开始使用广谱抗生素,包括万古霉素和美罗培南。自上次入院以来,RT - PCR检测呈阳性,抗sars - cov -2 IgG抗体呈阴性。动脉血气pH为7.41,PaCO2为63 mmHg, PaO2为60 mmHg, SaO2为91%。全血细胞计数显示血红蛋白10.1 g/L,白细胞16,800个,血培养无生长。胸部初始CT显示双侧弥漫性磨玻璃影,与新冠肺炎相符。随后,因呼吸衰竭加重,患者插管并机械通气,开始经验性米卡芬。支气管镜检查显示广泛的白色渗出膜覆盖气管和双主支气管。支气管活检标本和支气管清洗液显示烟曲霉。血清半乳甘露聚糖和真菌素呈阳性。米卡芬金改为异唑康唑,两天后患者发生难治性感染性休克。尽管使用了异戊康唑和支持性护理,急性恶化后出现难治性低氧血症和少尿,导致重症监护病房住院第6天发生致命的心脏骤停。曲霉菌性气管支气管炎是一种罕见的IPA表现,占病例的10%。这种情况的诊断非常困难,因此由于其相对非特异性的表现和缺乏特异性的影像学表现而延迟。该病例表明,在接受大剂量全身类固醇和免疫调节剂治疗的伴有潜在COVID - 19肺炎的患者中,需要仔细筛查机会性感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fatal Invasive Pulmonary Aspergillosis Associated with Coronavirus Disease 2019 (COVID 19) Infection
Aspergillus is a ubiquitous fungus that causes a variety of clinical syndromes in the lung. The type and severity of airway and parenchymal disease produced by Aspergillus are influenced by the patient's immunologic status and the presence of pre-existing lung disease. There is increasing concern that patients with coronavirus disease 2019 (COVID-19) might be at risk of developing invasive pulmonary aspergillosis co-infection particularly in the context of immunomodulatory monoclonal antibodies. We present a case report of pseudomembranous aspergillus tracheobronchitis complicated by COVID-19 pneumonia. A 59-year-old female with a medical history of drug-induced interstitial lung disease from methotrexate, rheumatoid arthritis, was admitted to the intensive care unit secondary to dyspnea and hypoxemic respiratory failure. She was diagnosed recently with COVID-19 pneumonia treated with remdesevir and high dose systemic corticosteroids for 14 days. one week after she is re-admitted with shortness of breath requiring high flow nasal cannula. she had a temperature of 38.2°, blood pressure of 110/80 mmHg, heart rate of 90 bpm, and respiratory rate of 30 breaths/min. Chest auscultation was significant for diffuse bilateral inspiratory coarse crackles. She was started on broad-spectrum antibiotics with vancomycin and meropenem. RT PCR COVID test remains positive since the last admission and Anti-SARS-CoV-2 IgG Antibodies are negative. Arterial blood gas values were pH 7.41, PaCO2 63 mmHg, PaO2 60 mmHg, and SaO2 91%. The complete blood count showed hemoglobin of 10.1 g/L and 16,800 leucocytes, with no growth in blood cultures. Initial CT chest reveals bilateral diffuse ground-glass opacities consistent with COVID pneumonia. Subsequently, she was intubated and mechanically ventilated for worsening respiratory failure, empiric micafungin was started. A bronchoscopy demonstrated extensive whitish exudative membranes covering the trachea and both mainstem bronchi. The endobronchial biopsy specimens and bronchial washing fluid revealed Aspergillus fumigatus. Serum Galactomannan and fungitel came back positive. Micafungin was changed to isavuconazole, two days later the patient developed refractory septic shock. Despite using isavuconazole and supportive care, acute deterioration followed with refractory hypoxemia and oliguria, resulting in a fatal cardiac arrest on the sixth day of the intensive care unit stay. Aspergillus tracheobronchitis is an unusual manifestation of IPA accounts for <10% of cases. diagnosis of this condition is extremely difficult and hence is delayed given its relatively nonspecific presentation and the lack of specific radiographic findings. This case illustrates a need for careful screening for opportunistic infections in patients treated with high-dose systemic steroids, immunomodulators with underlying COVID pneumonia.
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