covid - 19后晚发型纤维化1例报告

P. Modi, B. Tuppekar, G. Nair, A. Uppe
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引用次数: 0

摘要

虽然大多数COVID-19病例在2-6周内完全康复,但一些病例可能会出现包括残余肺纤维化在内的并发症。我们描述了一个有趣的迟发性covid后纤维化病例,该病例在初次感染后4个多月出现。病例:一名52岁男性,职业手术室技术人员,在2020年5月初与一名感染患者接触后,COVID-19检测呈阳性。他无症状,生命稳定,无合并症,给予一个疗程的口服羟氯喹、奥司他韦和多种维生素。患者在隔离病房无症状停留一周,各项检查正常,出院回家。第一次随访2周时HRCT胸部检查正常,患者在接下来的3个月恢复正常工作。9月中旬,患者因用力时突然出现呼吸困难,持续5天,室内空气氧饱和度为93%来到门诊。他无法进行6分钟步行测试(6MWT)。肺活量测定提示中度限制和DLCO降低。此时胸部HRCT显示双侧广泛网状影,双侧所有肺叶均有少量磨玻璃影(GGO’s),以基底部为主。这些结果提示在初次感染后4个多月后出现迟发性残留纤维化。RT-PCR检测结果为阴性,排除再次感染的可能。患者不愿入院,开始口服吡非尼酮,逐渐减少口服强的松龙剂量,并建议家庭吸氧治疗。他没有带氧回家,但口服类固醇和抗纤维化药物依从。在covid后随访的第7个月,HRCT显示与前一次扫描相比有显着改善,网状混浊物减少,GGO最小。患者症状较好,室内空气饱和度为98%,可以满意地进行6MWT。肺活量测定显示FVC轻度受限和改善。抗纤维化剂量加大,患者转介肺部康复治疗。尽管covid后后遗症的自然历史不确定,但据观察,covid后纤维化可早在初次感染后3周发生。该病例的独特之处在于在第二次随访时出现较晚,随访时间为4个月,第一次随访时影像学和临床参数正常。因此,应对所有患者进行细致的长期随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late Onset Post-COVID Fibrosis - A Case Report
Introduction: While most cases of COVID-19 recover completely within 2-6 weeks, some may develop complications including residual lung fibrosis. We describe an interesting case of late-onset post-COVID fibrosis that presented more than 4 months after the initial infection. Case: A 52-year-old male, an operating room technician by profession tested positive for COVID-19 after coming in contact with an infected patient early in May 2020. He was asymptomatic, vitally stable with no comorbidities, and was given a course of oral hydroxychloroquine, oseltamivir, and multivitamins. He remained asymptomatic for a week in the isolation ward with all investigations within normal range and was discharged home. HRCT thorax on the first follow-up at 2 weeks was normal and the patient resumed work as usual for the next 3 months. In mid-September, the patient presented to the outpatient clinic with a sudden onset of dyspnea on exertion that was progressive for 5 days with an oxygen saturation of 93% on room air. He was unable to perform a 6-minute walk test (6MWT). Spirometry was suggestive of moderate restriction and reduced DLCO. HRCT thorax at this point revealed bilateral extensive reticular opacities with few ground-glass opacities (GGO's) in all lobes bilaterally with a basal predominance. These findings were suggestive of late-onset of residual fibrosis more than 4 months after the initial infection. RT-PCR for COVID-19 was negative and ruled out re-infection. The patient was unwilling for admission and was started on oral pirfenidone, a tapering dose of oral prednisolone, and was advised home oxygen therapy. He did not take home oxygen but was compliant with oral steroids and antifibrotic. In the 7th-month of post-COVID follow-up, HRCT showed significant improvement as compared to the previous scan with reduced reticular opacities and minimal GGO's. The patient was symptomatically better with a saturation of 98% on room air and could perform 6MWT satisfactorily. Spirometry showed mild restriction and improvement in FVC. The antifibrotic dose was stepped up and the patient was referred for pulmonary rehabilitation. Discussion Despite an uncertain natural history of post-COVID sequelae, it has been observed that post-COVID fibrosis can develop as early as 3 weeks after the initial infection. This case was unique in its late presentation during the second post-COVID follow up at 4 months with normal imaging and clinical parameters during the first follow up. Hence a meticulous long-term follow-up should be done for all patients.
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