Department of Internal Medicine, New York Medical College, Metropolitan Hospital Center, New York City, NY, USA.
Division of Cardio-Nephrology, Cardiac Renal & Vascular Associates, Jackson, USA.
Am J Case Rep. 2023 Mar 16;24:e938359. doi: 10.12659/AJCR.938359.
BACKGROUND The management of (Coronavirus disease 2019) COVID-19 pneumonia is ever-evolving. Tocilizumab, a monoclonal antibody against interleukin-6 (IL-6) receptor, have known mortality benefit in severe COVID-19 pneumonia, but data are limited regarding safety. Attributable to the immunomodulatory nature of this medication, patients may be at risk for opportunistic infections, including chronic cavitary pulmonary aspergillosis (CPPA), a slowly progressive disease characterized pulmonary infiltrates and often a newly-formed cavity. However, current guidelines do not emphasize post-treatment surveillance of patients for opportunistic infections, including CPPA. CASE REPORT We present a particular case of a 64-year-old man treated for COVID-19 pneumonia with Tocilizumab and dexamethasone who developed cavitary pulmonary aspergillosis. He presented to the emergency department with hemoptysis, associated with worsening productive cough, shortness of breath, and weight loss. Computed tomography (CT) of the chest showed areas of focal consolidation and a cavitary lung lesion within the left upper lobe. Sputum culture was positive for Aspergillus niger. The patient received a long course of oral triazole therapy for CPPA, with clinical improvement. CT scan of the chest at 9 months showed that the Itraconazole therapy was effective in resolving the extensive airspace disease and decreasing the size of the upper-lobe cavity and fungal ball. CONCLUSIONS This article illustrates the possibility of a serious infection such as CCPA as an adverse effect of Tocilizumab treatment, especially with concurrent immunosuppressive therapy. Furthermore, this case highlights the importance of regular monitoring of patients who have received Tocilizumab therapy to ensure that early signs of opportunistic infections such as CPPA are detected and treated promptly to prevent permanent lung damage.
(2019 年冠状病毒病)COVID-19 肺炎的治疗方法在不断发展。托珠单抗是一种针对白细胞介素-6(IL-6)受体的单克隆抗体,在严重 COVID-19 肺炎中已被证实具有降低死亡率的作用,但关于其安全性的数据有限。由于这种药物具有免疫调节作用,患者可能有机会发生感染的风险,包括慢性空洞性肺曲霉病(CPPA),这是一种进展缓慢的疾病,其特征是肺部浸润,通常伴有新形成的空洞。然而,目前的指南并没有强调对接受托珠单抗和地塞米松治疗的 COVID-19 肺炎患者进行机会性感染(包括 CPPA)的治疗后监测。
我们报告了一例特殊的病例,一名 64 岁男性因 COVID-19 肺炎接受托珠单抗和地塞米松治疗后发生空洞性肺曲霉病。他因咯血、伴有进行性加重的咳痰、呼吸急促和体重减轻而到急诊就诊。胸部 CT 显示左肺上叶局灶性实变和空洞性肺病变。痰培养阳性为黑曲霉。患者接受了长期口服三唑类药物治疗 CPPA,临床症状得到改善。胸部 CT 扫描显示 9 个月时伊曲康唑治疗有效地解决了广泛的气腔疾病,缩小了上叶空洞和真菌球的大小。
本文说明了在接受托珠单抗治疗时,特别是同时接受免疫抑制治疗时,可能会发生严重感染,如 CPPA。此外,该病例强调了对接受托珠单抗治疗的患者进行定期监测的重要性,以确保及时发现 CPPA 等机会性感染的早期迹象,并进行治疗,以防止永久性肺损伤。