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Relapse of COVID-19 and Viral Evolution in a Patient With Good Syndrome: A Case Report.
Iwasaki, Mika; Hashimoto, Masao; Takeuchi, Junko S; Kusaba, Yusaku; Kimura, Moto; Terada-Hirashima, Junko; Sugiura, Wataru; Hojo, Masayuki.
Afiliação
  • Iwasaki M; Department of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, JPN.
  • Hashimoto M; Department of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, JPN.
  • Takeuchi JS; Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, JPN.
  • Kusaba Y; Department of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, JPN.
  • Kimura M; Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, JPN.
  • Terada-Hirashima J; Department of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, JPN.
  • Sugiura W; Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, JPN.
  • Hojo M; Department of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, JPN.
Cureus ; 16(1): e52592, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38371040
ABSTRACT
Delays in clearance and rapid evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been reported in immunocompromised patients. We encountered a case of recurrent, multi-mutational SARS-CoV-2 infection in a 40-year-old man with severe immunodeficiency due to Good syndrome. The patient had not received the SARS-CoV-2 vaccination. In August 2021, he was first admitted to the hospital owing to coronavirus disease 2019 (COVID-19) pneumonia and was administered dexamethasone, remdesivir, and baricitinib. Although his fever and respiratory condition improved once, chest computed tomography (CT) revealed extensive diffuse consolidation and ground-glass opacities (GGOs), and both methylprednisolone pulse therapy and tocilizumab yielded a limited effect. After a third course of remdesivir without immunosuppressants or steroids, the patient recovered, and he tested negative for SARS-CoV-2. On day 272 since the clinical onset, he was readmitted with dyspnea and mild fever due to a COVID-19 recurrence. He was infected with the Delta variant (AY.29), despite the Omicron (BA.2) variant being predominant at that time. During this admission, additional remdesivir and casirivimab/imdevimab yielded marked effects, and the SARS-CoV-2 quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) tests rapidly returned negative. Phylogenetic analysis demonstrated the accumulation of mutations, including those yielding remdesivir resistance, throughout the SARS-CoV-2 genome. Appropriate use of antivirals and monoclonal antibodies may aid in the recovery of patients with COVID-19 and immunodeficiency and in preventing the emergence of multi-mutational SARS-CoV-2 variants.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos