COVID-19感染背景下罕见的潜伏性结核再激活病例

G. Lee, J. Stoll, I. El Husseini
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引用次数: 5

摘要

几十年来,结核病(TB)仍然是全球由单一感染源导致死亡的主要原因。2020年,2019年冠状病毒病(COVID-19)大流行造成的死亡率超过了结核病的年死亡率。活动性COVID-19和结核病合并感染的影响尚不清楚。我们提出了在美国COVID-19感染背景下首次记录的活动性结核病病例之一。病例报告一名49岁男性,既往有纵隔灰色区淋巴瘤和高血压病史,并有腹泻和便血4天病史。病人于1995年从越南移民过来。ct示乙状结肠壁增厚,双侧肺磨玻璃影,符合新型冠状病毒肺炎,经聚合酶链反应(PCR)证实。由于最近的化疗,他也出现了嗜中性粒细胞减少。入院时,他开始出现缺氧加剧和劳累,并开始使用瑞德西韦和地塞米松治疗COVID-19感染。连续胸片显示双基底动脉混浊恶化。他继续有较高的氧气需求,高流量鼻插管和无呼吸机达到最大,氧饱和度为88-90%,需要转至重症监护病房。此时进行了一次完整的感染性检查。巨细胞病毒PCR在1486IU呈阳性,开始使用更昔洛韦。进行了支气管镜检查,但所有测试均为阴性,包括抗酸杆菌(AFB)涂片。患者持续出现越来越严重的缺氧、酸中毒和脓毒性,最终接受了气管切开术。支气管镜检查后20天,支气管肺泡液培养结核分枝杆菌(MTB)阳性。送新痰样本,发现涂片阳性(2+ AFB)和MTB PCR阳性。患者开始使用利福平、异烟肼、吡嗪酰胺和乙胺丁醇治疗。不幸的是,患者继续失代偿,无法脱离呼吸机。家属开始了舒适护理,患者于住院第68天去世。患者有潜伏性结核再激活的几个危险因素,包括恶性肿瘤、长期使用皮质类固醇和COVID-19感染。早期研究表明,与未患结核病的患者相比,患有既往结核病或活动性结核病的患者感染COVID-19的死亡风险和恢复时间可能更高。在COVID-19重症肺炎患者和多种免疫抑制危险因素中,除继发性重复感染外,还应考虑潜伏性结核再激活。
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A Rare Case of Latent Tuberculosis Reactivation in the Setting of COVID-19 Infection
Introduction For decades, tuberculosis (TB) remained the leading cause of mortality due to a single infectious agent globally. In 2020, mortality due to the coronavirus disease 2019 (COVID-19) pandemic exceeded annual rates of death from TB. The impact of active COVID-19 and TB co-infection remain unclear. We present one of the first documented cases of active TB in the setting of COVID-19 infection in the United States. Case Report A 49-year-old man with a past medical history of mediastinal gray zone lymphoma and hypertension presented to the emergency room with a four-day history of diarrhea and hematochezia. The patient immigrated from Vietnam in 1995. Computed tomography imaging revealed thickening of the sigmoid wall, and bilateral pulmonary ground glass opacities consistent with COVID-19 pneumonia, which was confirmed by polymerase chain reaction (PCR). He was also neutropenic from recent chemotherapy. On admission, he began experiencing worsening hypoxia with exertion, and was started on remdesivir and dexamethasone for COVID-19 infection. Serial chest radiographs revealed worsening bibasilar opacities. He continued to have higher oxygen requirements and maxed out on high-flow nasal cannula and non-rebreather with 88-90% oxygen saturation, requiring transfer to the intensive care unit. A complete infectious workup was performed at this point. Cytomegalovirus PCR was positive at 1486IU and was started on ganciclovir. A bronchoscopy was performed but all testing was negative, including that for acid-fast bacilli (AFB) smear. The patient continued to become increasingly hypoxic, acidotic, and septic, and eventually underwent tracheostomy. Twenty days post-bronchoscopy, cultures from the bronchoalveolar fluid came back positive for Mycobacterium tuberculosis (MTB). A new sputum sample was sent and was found to be smear positive (2+ AFB) and MTB PCR positive. The patient was initiated on rifampin, isoniazid, pyrazinamide, and ethambutol therapy. Unfortunately, the patient continued to decompensate and was unable to be weaned off the ventilator. Comfort care was initiated by the family and the patient passed away on hospital day 68. Discussion The patient had several risk factors for latent TB reactivation, including malignancy, long-term corticosteroid use, and COVID-19 infection. Early research has shown that risk of death and recovery time with COVID-19 may be higher in patients with previous or active TB compared to those without. In patients with severe COVID-19 pneumonia and multiple risk factors for immunosuppression, latent TB reactivation should be considered in addition to secondary superinfection.
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