Differentiating Multisystem Inflammatory Syndrome in Children (MIS-C) and Its Mimics - A Single-Center Experience

S Balasubramanian1, Janani Sankar1, K Dhanalakshmi1

  • 1Department of Paediatrics, Kanchi Kamakoti CHILDS Trust Hospital, Chennai, Tamil Nadu, India.

Indian Pediatrics
|March 10, 2023
PubMed

Insights

Identifying multisystem inflammatory syndrome in children (MIS-C) requires specific clinical and laboratory markers. Older age, mucocutaneous symptoms, high C-reactive protein, and neutrophilic leukocytosis favor MIS-C diagnosis over other febrile illnesses.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Clinical Medicine

Background:

  • Multisystem inflammatory syndrome in children (MIS-C) is a rare but serious condition.
  • Accurate and timely diagnosis is crucial for effective management.
  • Distinguishing MIS-C from other febrile illnesses can be challenging, especially in tropical settings.

Purpose of the Study:

  • To identify clinical and laboratory indicators that differentiate MIS-C from other febrile diseases in a tropical hospital.
  • To aid in the early and accurate diagnosis of MIS-C.

Main Methods:

  • Retrospective review of hospital records from April 2020 to June 2021.
  • Analysis of laboratory values, SARS-CoV-2 serological status, clinical signs, and symptoms.
  • Comparison between children diagnosed with MIS-C and those with similar presentations.

Main Results:

  • 114 children met inclusion criteria; 64 were diagnosed with MIS-C, and 50 had other infections (enteric fever, scrub typhus, dengue, appendicitis).
  • Key differentiating features for MIS-C included older age, mucocutaneous symptoms, elevated C-reactive protein, neutrophilic leukocytosis, and abdominal pain.
  • Absence of hepatosplenomegaly was also noted as favoring MIS-C.

Conclusions:

  • Older age, mucocutaneous symptoms, high C-reactive protein, neutrophilic leukocytosis, and abdominal pain are strong indicators for MIS-C.
  • Absence of hepatosplenomegaly can also support a MIS-C diagnosis.
  • These findings assist in differentiating MIS-C from mimic febrile diseases in pediatric populations.
Abstract