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.

Turk Patoloji Dergisi
|June 23, 2026
PubMed

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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