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Aspergillus tracheobronchitis: Report of 8 cases and review of the literature

机译:气管曲霉菌支气管炎8例报告并文献复习

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Aspergillus tracheobronchitis (AT) is an infrequent but severe form of invasive pulmonary aspergillosis in which the fungal infection is entirely or predominantly confined to the tracheobronchial tree. We reviewed 8 cases of AT diagnosed in our tertiary care center during an 18-year period, as well as 148 cases previously reported in the English literature from 1985 to July 2011. The demographic, clinical, imaging, bronchoscopic, and outcome characteristics of every eligible patient were excerpted, and predictors of inhospital mortality were identified by logistic regression. Solid organ transplantation (SOT) (44.2%), hematologic malignancy (21.2%), neutropenia (18.7%), and chronic obstructive pulmonary disease (15.4%) were the most common underlying conditions reported. Most cases occurred in patients receiving long-term corticosteroid treatment (71.8%) or chemotherapy (25.0%). Fever and respiratory complaints (cough, dyspnea, stridor, or wheezing) were the most frequent symptoms; one-third of patients developed acute respiratory distress at presentation, and 15.1% were asymptomatic at the time of diagnosis. Initial imaging studies were not informative in 47.4% of the cases. Aspergillus fumigatus was the predominant species (74.4%). The pseudomembranous form was the most commonly observed (31.9% of cases) and was more frequent in neutropenic patients (p = 0.007), whereas ulcerative AT (31.2%) was associated with SOT (p = 0.001). The most frequent antifungal monotherapy regimens were amphotericin B deoxycholate (23.1%) and itraconazole (18.6%), whereas combined therapy was administered in 35.9% of the cases. Overall inhospital mortality was 39.1%, with neutropenia (odds ratio [OR], 20.47; p < 0.001) and acute respiratory distress at presentation (OR, 9.54; p = 0.002) as independent prognostic factors. Our pooled analysis of the literature shows that AT remains a rare opportunistic infection with a nonspecific presentation and a variable course depending on the nature of the predisposing factor.
机译:气管支气管曲霉(AT)是一种罕见但严重的侵袭性肺曲霉病,其中真菌感染完全或主要限于气管支气管树。我们回顾了18年来在我们的三级护理中心诊断出的8例AT,以及1985年至2011年7月以前在英国文献中报道的148例。符合条件的患者摘录,并通过逻辑回归确定院内死亡率的预测因子。实体器官移植(SOT)(44.2%),血液系统恶性肿瘤(21.2%),中性粒细胞减少症(18.7%)和慢性阻塞性肺疾病(15.4%)是最常见的基础疾病。大多数病例发生在接受长期糖皮质激素治疗(71.8%)或化疗(25.0%)的患者中。发烧和呼吸系统不适(咳嗽,呼吸困难,喘鸣或喘息)是最常见的症状。三分之一的患者在就诊时出现了急性呼吸窘迫,在诊断时为无症状的15.1%。最初的影像学检查对47.4%的病例没有帮助。烟曲霉是主要种类(74.4%)。假膜形式是最常见的(占病例的31.9%),在中性粒细胞减少的患者中更为常见(p = 0.007),而溃疡性AT(31.2%)与SOT相关(p = 0.001)。最常见的抗真菌单药治疗方案是两性霉素B脱氧胆酸盐(23.1%)和伊曲康唑(18.6%),而35.9%的病例采用联合治疗。总体住院死亡率为39.1%,中性粒细胞减少(几率[OR],20.47; p <0.001)和急性呼吸窘迫(OR,9.54; p = 0.002)是独立的预后因素。我们对文献的汇总分析表明,AT仍然是一种罕见的机会感染,具有非特异性表现,并且取决于易感因素的性质,其病程也可变。

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