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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
Summary
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.
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