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Case report: Thrombotic microangiopathy in pediatric multisystem inflammatory syndrome associated with COVID-19: a
Hülya Nalçacıoğlu1, H Gözde Önal1, Burcu Bozkaya Yücel2
1Pediatric Nephrology Department, Ondokuz Mayis University Faculty of Medicine, Samsun, Türkiye.
Insights
Multisystem inflammatory syndrome in children (MIS-C) can trigger thrombotic microangiopathy (TMA) in pediatric COVID-19 cases. Early intervention is crucial for managing this serious complication and improving patient outcomes.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Hematology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a post-infectious complication of COVID-19.
- Thrombotic microangiopathy (TMA) is a serious condition characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ damage.
- The association between MIS-C and TMA in pediatric populations requires further investigation.
Introduction:
This report provides insight into three distinct pediatric cases exhibiting a nexus between multisystem inflammatory syndrome in children (MIS-C) and thrombotic microangiopathy (TMA) triggered by COVID-19. The aim is to underscore the range of clinical presentations and the essentiality of early interventions.
Case Presentations:
This report presents three cases aged 10 months, 7 years, and 3 years with persistent fever, diarrhea, nausea, and vomiting. The first case, a 10-month-old girl, demonstrated acute kidney injury (AKI) and microangiopathic hemolytic anemia (MAHA) following a COVID-19 infection. Despite initial negative SARS-CoV-2 RT-PCR results, her condition escalated rapidly, presenting increased levels of LDH (peaking at 4,200 U/L) and requiring renal replacement therapy (RRT) to manage deteriorating renal function. Interventions with eculizumab and anakinra led to marked improvements, with a stable follow-up of 13 months post-hospitalization. The second case involved a 7-year-old girl who developed symptoms of MIS-C, hemolytic uremic syndrome (HUS), and posterior reversible encephalopathy syndrome (PRES) post-exposure to COVID-19, evidenced by heightened LDH levels (3,522 U/L at peak). After a precarious period of deteriorating kidney function and exacerbated hypertension, she responded positively to treatments, inclusive of IVIG, steroid therapies, and eculizumab, with a favorable 6-month follow-up showcasing stable laboratory results. The third case discusses a 3-year-old boy, without any medical history, manifesting HUS symptoms and COVID-19 infection. He exhibited increased LDH levels (peaking at 3,946 U/L) alongside elevated creatinine, marking renal impairment. He responded well to hemodialysis, IVIG, and steroid therapy, showcasing substantial recovery by the 19th day of hospitalization, which marked his discharge with a tapering steroid regimen.
Conclusion:
This case series underscores that MIS-C-associated TMA is a significant complication in pediatric COVID-19. Our findings illuminate the potential for treatment success but simultaneously emphasize the need for a more comprehensive understanding of the underlying pathophysiology.
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