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Pre-Mortem Histopathologic Evidence of Endothelial Injury and Thrombotic Microangiopathy in an Infant With
Meral Uner1, Fariba Amini1, Sefika Karabulut2
1Department of Pathology, Hacettepe University Faculty of Medicine, ANKARA, TÜRKİYE.
Abstract:
Multisystem inflammatory syndrome in children (MIS-C) represents a severe postinfectious hyperinflammatory condition following SARS-CoV-2 infection. Despite extensive clinical characterization, histopathologic data-especially from pre-mortem pediatric biopsies-remain scarce. We report a 9-month-old male infant with confirmed SARS-CoV-2 infection and rapid multiorgan failure. Pre-mortem incisional biopsies from the myocardium, lung, and pleura revealed degenerative myocyte changes, endothelial swelling, and fibrin-platelet microthrombi consistent with thrombotic microangiopathy. Immunohistochemistry demonstrated mild CD3+ T-cell-predominant infiltrates and focal SARS-CoV-2 antigen positivity confined to alveolar and bronchiolar epithelium, while myocardial and pleural tissues were negative. These findings highlight early morphologic correlates of immune-mediated vascular injury in MIS-C, characterized by endothelial dysfunction, microvascular inflammation, and T-cell-driven immunopathology in the absence of direct viral cytopathy. This case provides rare pre-mortem evidence of immune-thrombotic endotheliopathy in an infant, bridging clinical and histologic manifestations of pediatric SARS-CoV-2-associated hyperinflammatory disease.
Insights
Multisystem inflammatory syndrome in children (MIS-C) involves post-SARS-CoV-2 hyperinflammation. Pre-mortem infant biopsies reveal immune-mediated vascular injury, endothelial dysfunction, and microthrombi, not direct viral damage.
Area of Science:
- Pediatric Pathology
- Immunology
- Infectious Diseases
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a severe post-SARS-CoV-2 hyperinflammatory condition.
- Histopathologic data from pre-mortem pediatric biopsies in MIS-C are limited.
- Understanding the early morphologic changes is crucial for diagnosis and treatment.
Purpose of the Study:
- To report histopathologic findings from pre-mortem biopsies in an infant with MIS-C and multiorgan failure.
- To characterize the early vascular and inflammatory changes associated with MIS-C.
- To investigate the role of viral presence versus immune-mediated injury.
Main Methods:
- Analysis of pre-mortem incisional biopsies (myocardium, lung, pleura) from a 9-month-old male infant.
- Histopathologic examination including light microscopy and immunohistochemistry.
- Detection of SARS-CoV-2 antigens via immunohistochemistry.
Main Results:
- Biopsies showed degenerative myocyte changes, endothelial swelling, and microthrombi consistent with thrombotic microangiopathy.
- Immunohistochemistry revealed mild T-cell infiltrates and focal SARS-CoV-2 antigen positivity in respiratory epithelium.
- Myocardial and pleural tissues were negative for SARS-CoV-2 antigens, suggesting limited direct viral involvement.
Conclusions:
- Findings indicate early immune-mediated vascular injury in MIS-C, characterized by endothelial dysfunction and microvascular inflammation.
- The study provides rare pre-mortem evidence of immune-thrombotic endotheliopathy in an infant with MIS-C.
- Pathology is driven by T-cell immunopathology rather than direct viral cytopathy in affected tissues.
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