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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.
Abstract:
Multisystem inflammatory syndrome (MIS) is a new and rare complication of COVID-19 that usually occurs in children. An increasing number of cases of MIS in adults are described in the literature. The condition is associated with high mortality, and treatment is non-standardized. Clinical pictures are heterogeneous, and diagnosis is very challenging. Here we describe a case of MIS in a 60-year-old man with previous follicular lymphoma treated with obinutuzumab and recent SARS-CoV-2 infections. He complained of an unknown fever and developed pancytopenia during the hospitalization, associated with a general clinical worsening. The patient was successfully treated with intravenous immunoglobulin and steroids.
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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