covid后组织肺炎

D. Ford, R. Holladay, T. Sartawi, P. Charoenpong, J. D. Packer, K. K. Goddard
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引用次数: 2

摘要

新型SARS冠状病毒2 (SARS- cov -2)感染的无数急性临床病理效应正在被描述。在这里,我们提出了一个病例报告,说明活检证实了Covid-19疾病的明显慢性并发症,折磨了一些幸存者:Covid-19后组织性肺炎(PCOP)。一名30岁的非洲裔美国女性,已知感染人类免疫缺陷病毒(HIV),接受抗逆转录病毒治疗(ART),最近诊断为结节性边缘区淋巴瘤,接受化疗,于2020年8月初感染了SARS-Cov-2。患者表现为发热、咳嗽加重和呼吸急促,两周后病情加重。在急诊室,她体温102华氏度,心率110,室内空气氧饱和度88%。白细胞增多17.62 k/uL,近期绝对CD4 590/mm3。SARSCoV-2聚合酶链反应(PCR)阳性。入院胸片显示双侧基底混浊,符合Covid-19肺炎。我们的病人入院并接受地塞米松和一个疗程的经验性抗生素治疗社区获得性肺炎。患者以短暂口服强的松减量治疗出院,家用吸氧2L/min;然而,在接下来的8周内,她又因类似的咳嗽、反复发热和呼吸困难并在一系列胸部影像学上出现新的局灶性混浊而再次入院两次(图1)。尽管使用了广泛的经验抗生素包括抗真菌治疗,但她的症状仍然存在。继发性感染和自身免疫性疾病的大量实验室检查未显示。最后进行支气管镜检查和经支气管低温活检(TBC),发现急性和慢性炎症伴间质纤维化。支气管肺泡灌洗(BAL)培养阴性。正如系列影像所证明的(图1),我们的患者使用经验性类固醇治疗组织性肺炎持续改善。她的临床发现再次出现,甚至在SARS-CoV-2 PCR最初呈阳性的5个月后,她也试图减少类固醇的使用。本病例说明了Covid-19后组织性肺炎(PCOP)。这是一种临床病理综合征,其特点是使用皮质类固醇可迅速缓解,但当逐渐减少或停止治疗时,复发频繁它还说明了照顾急性SARS-CoV-2感染患者的几个突出问题:1)与慢性免疫抑制相关的延迟病毒清除,2)延迟支气管镜检查以减轻护理提供者的感染风险,3)持续治疗对后续延迟病理发现的影响,3 iv)与疾病晚期识别和我们在组织性肺炎背景下逐渐减少慢性类固醇治疗相关的发病率增加,以及5)早期活检的可能性,诊断和不间断的治疗可以预防肺纤维化。
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Post-Covid Organizing Pneumonia
A myriad of acute clinicopathological effects of novel SARS Coronavirus 2 (SARS-Cov-2) infection are being described. Here, we present a case report which illustrates a biopsy proven distinct chronic complication of Covid-19 disease which afflicts some survivors: Post Covid-19 Organizing Pneumonia (PCOP). A 30 year old African-American female with known Human Immunodeficiency Virus (HIV) infection on anti-retroviral therapy (ART) and recently diagnosed nodular marginal zone lymphoma, on chemotherapy, became infected with SARS-Cov-2 in early August, 2020. She presented with fever, increased cough, and shortness of breath worsening over two weeks. In the emergency room, she had temperature 102o F, heart rate of 110 with oxygen saturation 88% on room air. Lab work was significant for Leukocytosis of 17.62 k/uL and recent absolute CD4 of 590/mm3. SARSCoV-2 Polymerase Chain Reaction (PCR) test was positive. Admission Chest Roentgenogram (X-ray) revealed bilateral basal opacities consistent with Covid-19 Pneumonia. Our patient was admitted and received Dexamethasone and a course of empiric antibiotics for community acquired pneumonia. She was discharged on brief oral prednisone taper with home oxygen 2L/min;However, she would be readmitted to hospital twice more over the next eight weeks with similar complaints of cough, recurrent fever, and dyspnea with new focal opacities on serial chest imaging (Figure 1). Her symptoms persisted despite broadened empiric antibiotics including antifungal therapy. Extensive lab work-up for secondary infection and autoimmune disease was unrevealing. Bronchoscopy was finally done with Transbronchial Cryobiopsy (TBC) revealing acute and chronic inflammation with interstitial fibrosis. Bronchoalveolar lavage (BAL) cultures were negative. As evidenced by serial imaging (Figure 1), our patient consistently improved with empiric steroids for organizing pneumonia. Her clinical findings recurred with attempts to taper steroids even at five months post initial positive SARS-CoV-2 PCR. This case illustrates Post Covid-19 Organizing Pneumonia (PCOP). It is a Clinicopathologic syndrome characterized by rapid resolution with corticosteroids, but frequent relapses when treatment is tapered or stopped.1 It also illustrates several salient issues in caring for patients who survive acute SARS-CoV-2 infection: i) Delayed viral clearance related to chronic immunosuppression,2 ii) Delayed Bronchoscopy in an effort to mitigate infection risk to care providers, iii) The impact of ongoing therapy on consequent delayed pathology findings,3 iv) Increased morbidity associated with both late disease recognition and our attempts to taper chronic steroid therapy in the setting of an Organizing Pneumonia4 and v) The possibility that earlier biopsy, diagnosis and uninterrupted therapy may prevent pulmonary fibrosis.
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