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Published on: March 14, 2017
Multisystem inflammatory syndrome in children with COVID-19 in a multitransfused patient
Swarnalata Das1, Manas Behera Ranjan1, Palash Das1
1Departments of Pediatrics, Kalinga Institute of Medical Sciences, KIIT University, Bhubaneshwar, Odisha, India.
Insights
Multi-system inflammatory syndrome in children (MIS-C) associated with COVID-19 can occur in children with transfusion-dependent thalassemia. Early MIS-C diagnosis in these complex cases is crucial for prompt treatment and recovery.
Area of Science:
- Pediatric Hematology
- Infectious Diseases
- Critical Care Medicine
Background:
- Multi-system inflammatory syndrome in children (MIS-C) is a rare but serious condition linked to COVID-19.
- Transfusion-dependent thalassemia, particularly Beta thalassemia major, requires lifelong transfusions and iron chelation therapy.
- Iron overload in thalassemia patients can elevate ferritin levels, complicating the diagnosis of inflammatory conditions.
Observation:
- A 3-year-old boy with Beta thalassemia major presented with acute respiratory distress and abdominal pain.
- The patient exhibited signs of severe anemia, elevated acute phase reactants, and a significant, unexplained rise in serum ferritin levels despite iron chelation.
- SARS-CoV-2 antibody testing was positive, raising suspicion for MIS-C.
Findings:
- The clinical presentation and laboratory findings, including the sharp increase in ferritin, were consistent with MIS-C.
- Diagnosis of MIS-C in the context of thalassemia requires high clinical suspicion due to overlapping symptoms and laboratory markers.
- The patient responded well to intravenous corticosteroid treatment.
Implications:
- This case highlights the importance of considering MIS-C in children with thalassemia who present with acute illness and elevated ferritin.
- Prompt diagnosis and management of MIS-C are essential for favorable outcomes in these vulnerable patients.
- Unexplained ferritin surges in multi-transfused patients warrant thorough investigation for concurrent inflammatory conditions like MIS-C.
Abstract:
Multi-system inflammatory syndrome in children associated with COVID19 (MIS-C) is a unique clinical syndrome characterised by fever, gastrointestinal symptoms, skin and oral rash and or neurological symptoms in the presence of raised acute phase reactants and coagulopathy. Ferritin is an acute phase reactant which is used as a marker of inflammation. Diagnosis of MIS-C in the background of transfusion dependent thalassemia with iron overload needs a strong clinical suspicion. Early diagnosis and prompt treatment are necessary to ensure a rapid uneventful recovery. A three-year-old male child born to non-consanguineously related parents reported to pediatric emergency with difficulty breathing and pain abdomen for one day. The child was a diagnosed case of Beta thalassemia major since the age of one year and was on regular transfusions and was on iron chelation for past eleven months with deferrasirox. Initial clinical examination showed a sick and irritable child with tachypnea tachycardia and hypoxia. Initial investigations showed raised acute phase reactants along with severe anemia. The child was investigated for MIS-C because of unexpected rise of serum ferritin from 1980 ng/mL (October 2020) to 6686 ng/mL (in January 2021) despite being on regular chelation. Antibody titre for SARS COVID-19 was positive. The patient was treated with intravenous corticosteroids and improved with the same. The advent of COVID19 pandemic saw most children having a mild disease with no or minimal symptoms. Some kids however presented with more serious delayed symptoms of MIS-C. To diagnose same in multi transfused patients a strong clinical suspicion and just judgement based on the clinical and laboratory findings should be done. Unexplained rise in ferritin levels, typical symptoms and high probability of exposure to COVID19 helped in clinching diagnosis.
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