Multisystem Inflammatory Syndrome: A Case in an Adult With Controlled Lymphoma and a Persistent SARS-CoV-2 Infection

Luca Pipitò1,2, Alice Medaglia1, Irene Russotto1,2

  • 1Department of Infectious and Tropical Diseases, Azienda Ospedaliera Universitaria Policlinico (AOUP) Paolo Giaccone, Palermo, ITA.

Cureus
|July 24, 2023
PubMed

Insights

Multisystem inflammatory syndrome (MIS) is a rare COVID-19 complication. This case highlights successful treatment of MIS in an adult with lymphoma using immunoglobulin and steroids.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Oncology

Background:

  • Multisystem inflammatory syndrome (MIS) is a rare but serious complication of SARS-CoV-2 infection, primarily reported in children.
  • While less common, MIS in adults is increasingly recognized, presenting diagnostic challenges and high mortality rates.
  • Standardized treatment protocols for MIS are still lacking, necessitating case-based evidence.

Observation:

  • A 60-year-old male with a history of follicular lymphoma, treated with obinutuzumab, presented with unexplained fever following SARS-CoV-2 infection.
  • During hospitalization, the patient developed pancytopenia and general clinical deterioration, indicative of a severe systemic inflammatory process.
  • The clinical presentation was complex due to the patient's underlying malignancy and prior treatment.

Findings:

  • The patient was diagnosed with MIS, a condition characterized by widespread inflammation affecting multiple organ systems.
  • Prompt administration of intravenous immunoglobulin and corticosteroids led to a significant clinical improvement.
  • This case demonstrates the successful management of MIS in an immunocompromised adult patient.

Implications:

  • This case underscores the importance of considering MIS in adults, particularly those with underlying conditions or recent infections.
  • The successful treatment highlights the potential efficacy of immunoglobulin and steroid therapy in managing severe MIS cases.
  • Further research is needed to elucidate the pathophysiology of MIS in adults and optimize treatment strategies.

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