Imaging of Multisystem Inflammatory Disease in Children (MIS-C) Associated With COVID-19

Figen Palabiyik1, Nihal Akcay2, Esra Sevketoglu2

  • 1University of Health Sciences, Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Department of Pediatric Radiology, Istanbul, Turkey.

Academic Radiology
|July 21, 2021
PubMed

Insights

Imaging in pediatric multisystem inflammatory disease (MIS-C) associated with COVID-19 shows varied findings across systems. While not diagnostic, these radiological signs aid in evaluating affected organs and guiding treatment for MIS-C.

Area of Science:

  • Pediatric Radiology
  • Infectious Diseases
  • Inflammatory Diseases

Background:

  • Multisystem inflammatory disease in children (MIS-C) is a serious condition linked to COVID-19.
  • Understanding the spectrum of imaging findings in MIS-C is crucial for diagnosis and management.

Purpose of the Study:

  • To retrospectively evaluate and characterize the imaging findings in pediatric patients diagnosed with MIS-C.
  • To correlate radiological findings with affected organ systems in MIS-C.

Main Methods:

  • Retrospective analysis of imaging studies in 45 pediatric patients diagnosed with MIS-C.
  • Evaluated chest X-ray, echocardiography, abdominal radiographs, CT, MRI, and MRCP.
  • Findings were categorized by affected organ system.

Main Results:

  • Common chest X-ray findings included perihilar opacity and peribronchial thickening; pleural effusion was frequent on thorax CT.
  • Echocardiography revealed myocarditis in 31% of cases.
  • Abdominal findings included hepatosplenomegaly, gallbladder wall and periportal edema, mesenteric lymphadenopathy, and bowel wall thickening. Neurological findings included reversible splenial lesion syndrome (RESLES) and ADEM-like lesions.

Conclusions:

  • Radiological findings in pediatric MIS-C are diverse and system-dependent.
  • No single imaging finding is specific for MIS-C.
  • Imaging plays a supportive role in assessing organ involvement and guiding treatment strategies.
Abstract

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