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Giant Cell Myocarditis in Children: Elusive Giant Cells Might Not Be the Only Clue
Chrystalle Katte Carreon1, Jonathon A Hagel2,3, Kevin P Daly3,4
1Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Insights
Giant cell myocarditis (GCM) is a rare, aggressive heart condition. Initial cardiac biopsies in pediatric patients often yield inconclusive results, delaying definitive diagnosis and treatment.
Area of Science:
- Pediatric Cardiology
- Cardiac Pathology
- Rare Diseases
Background:
- Giant cell myocarditis (GCM) is a severe, rapidly progressing form of fulminant myocarditis.
- GCM has a high mortality rate, particularly in pediatric populations.
- Diagnosis can be challenging due to atypical presentations and initial biopsy findings.
Purpose of the Study:
- To present two pediatric cases of Giant Cell Myocarditis (GCM).
- To highlight similarities in clinical presentation and initial cardiac biopsy findings.
- To underscore the diagnostic challenges associated with GCM in children.
Main Methods:
- Retrospective review of two pediatric cases diagnosed with GCM over 20 years.
- Analysis of clinical presentations.
- Histopathological examination of initial cardiac biopsy samples.
Main Results:
- Only two pediatric cases of GCM were definitively diagnosed institutionally over two decades.
- Initial cardiac biopsies in both patients were histologically similar but inconclusive for GCM.
- Patients presented with similar clinical features, complicating early diagnosis.
Conclusions:
- Giant cell myocarditis is rare in children, with diagnostic delays common.
- Initial cardiac biopsies may not provide definitive GCM diagnosis, necessitating further investigation.
- Recognizing similar clinical and initial histopathological patterns is crucial for timely GCM diagnosis in pediatric patients.
Abstract:
Giant cell myocarditis (GCM) is a form of fulminant myocarditis that is rapidly progressive and frequently lethal even in children. Over the course of 20 years, a definitive histopathologic diagnosis of GCM has been made at our institution in only two pediatric patients, and in neither instance was the diagnosis of GCM rendered on initial cardiac biopsy. We present the two patients and highlight the similarities in their clinical presentation and their challenging and inconclusive- albeit histologically similar- initial cardiac biopsy findings.
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