Case Report: Fatal Acute Liver Failure With Giant Cell Transformation in a Pediatric Patient Associated With MIS-C

Carolina Bonilla Gonzalez1, Marcela Hincapié Echeverría2, Rocio Plazas Pachón2

  • 1Pediatric Intensive Care Unit, Department of Pediatrics, Fundación Santafe of Bogotá, Bogotá, Colombia.

Frontiers in Pediatrics
|February 7, 2022
PubMed

Insights

This study reports the first pediatric case of a 10-month-old boy with pediatric multi-system inflammatory syndrome (MIS-C) who experienced acute liver failure with giant cell transformation, leading to a fatal outcome despite treatment.

Area of Science:

  • Pediatric Gastroenterology and Hepatology
  • Infectious Diseases
  • Critical Care Medicine

Background:

  • Multi-system inflammatory syndrome in children (MIS-C) is a rare but serious condition.
  • Acute liver failure is an uncommon but severe complication of MIS-C.
  • This case highlights the potential for severe hepatic involvement in pediatric MIS-C.

Observation:

  • A 10-month-old boy presented with symptoms consistent with MIS-C.
  • The patient developed fulminant acute liver failure.
  • Diagnostic workup excluded other common causes of liver failure.

Findings:

  • The liver failure was characterized by giant cell transformation.
  • Despite standard treatment for liver failure, the patient had a fatal outcome.
  • Autopsy confirmed giant cell transformation as a key pathological finding.

Implications:

  • This case underscores the critical need for early recognition and management of MIS-C.
  • Understanding the spectrum of MIS-C complications, including severe liver injury, is crucial.
  • Further research is needed to elucidate the mechanisms of MIS-C-associated liver failure and improve patient outcomes.

Related Concept Videos