An autopsy study of the spectrum of severe COVID-19 in children: From SARS to different phenotypes of MIS-C. (May 2021)

• Record Type: Journal Article
• Authors: Duarte-Neto, Amaro Nunes; Caldini, Elia Garcia; Gomes-Gouvêa, Michele Soares; Kanamura, Cristina Takami; de Almeida Monteiro, Renata Aparecida; Ferranti, Juliana Ferreira; Ventura, Andrea Maria Cordeiro; Regalio, Fabiane Aliotti; Fiorenzano, Daniela Matos; Gibelli, Maria Augusta Bento Cicaroni; Carvalho, Werther Brunow de; Leal, Gabriela Nunes; Pinho, João Renato Rebello; Delgado, Artur Figueiredo; Carneiro-Sampaio, Magda; Mauad, Thais; Ferraz da Silva, Luiz Fernando; Saldiva, Paulo Hilario Nascimento; Dolhnikoff, Marisa
• Is Part Of: EClinicalMedicine. Volume 35(2021)
• Publication Date: 2021-05
• Subjects: Covid-19 -- Sars-cov-2 -- Autopsy -- Pathology -- Minimally invasive autopsy -- Children -- MIS-C, multisystem inflammatory syndrome in children; Medicine -- Research -- Periodicals; Medical policy -- Periodicals; Clinical Medicine; Health Policy; Public Health; Medical policy; Medicine -- Research; Periodical; Electronic journals; Periodicals; 613
• DOI: 10.1016/j.eclinm.2021.100850
• Languages: English
• ISSNs: 2589-5370

Abstract

Abstract: Background: COVID-19 in children is usually mild or asymptomatic, but severe and fatal paediatric cases have been described. The pathology of COVID-19 in children is not known; the proposed pathogenesis for severe cases includes immune-mediated mechanisms or the direct effect of SARS-CoV-2 on tissues. We describe the autopsy findings in five cases of paediatric COVID-19 and provide mechanistic insight into the mechanisms involved in the pathogenesis of the disease. Methods: Children and adolescents who died with COVID-19 between March 18 and August 15, 2020 were autopsied with a minimally invasive method. Tissue samples from all vital organs were analysed by histology, electron microscopy (EM), reverse-transcription polymerase chain reaction (RT-PCR) and immunohistochemistry (IHC). Findings: Five patients were included, one male and four female, aged 7 months to 15 years. Two patients had severe diseases before SARS-CoV-2 infection: adrenal carcinoma and Edwards syndrome. Three patients were previously healthy and had multisystem inflammatory syndrome in children (MIS-C) with distinct clinical presentations: myocarditis, colitis, and acute encephalopathy with status epilepticus. Autopsy findings varied amongst patients and included mild to severe COVID-19 pneumonia, pulmonary microthrombosis, cerebral oedema with reactive gliosis, myocarditis, intestinal inflammation, and haemophagocytosis. SARS-CoV-2 was detected in all patients in lungs, heart and kidneys by at least one method (RT-PCR, IHC or EM), and in endothelial cells from heart and brain in two patients with MIS-C (IHC). In addition, we show for the first time the presence of SARS-CoV-2 in the brain tissue of a child with MIS-C with acute encephalopathy, and in the intestinal tissue of a child with acute colitis. Interpretation: SARS-CoV-2 can infect several cell and tissue types in paediatric patients, and the target organ for the clinical manifestation varies amongst individuals. Two major patterns of severe COVID-19 were observed: a primarily pulmonary disease, with severe acute respiratory disease and diffuse alveolar damage, or a multisystem inflammatory syndrome with the involvement of several organs. The presence of SARS-CoV-2 in several organs, associated with cellular ultrastructural changes, reinforces the hypothesis that a direct effect of SARS-CoV-2 on tissues is involved in the pathogenesis of MIS-C. Funding: Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Bill and Melinda Gates Foundation.