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Quantitative Visualization of Leukocyte Infiltrate in a Murine Model of Fulminant Myocarditis by Light Sheet Microscopy
Published on: May 31, 2017
A cluster of fulminant myocarditis cases in children, Baltimore, Maryland, 1997
A W Mounts1, S Amr, R Jamshidi
1Viral Gastroenteritis Section, Respiratory and Enteric Viruses, Division of Viral and Rickettsial Diseases, National Center for Infectious Disease, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Insights
A rare cluster of pediatric myocarditis cases occurred in Baltimore in 1997. This fulminant disease in children led to a high mortality rate, with no infectious cause identified.
Area of Science:
- Pediatric Cardiology
- Epidemiology
- Pathology
Background:
- Estimating the true incidence of pediatric myocarditis is challenging due to undetected mild cases.
- Prior to 1997, the highest reported number of pediatric myocarditis deaths in a single year was three.
Observation:
- An unusual cluster of nine pediatric cases with myocarditis or similar clinical presentation and myocardial fibrosis was identified in the greater Baltimore area between May and October 1997.
- The affected children were predominantly Black and male, with no identifiable risk factors.
- The disease presented with a fulminant course, characterized by malignant arrhythmias and high mortality.
Findings:
- Seven cases of active myocarditis and two cases with myocardial fibrosis were diagnosed.
- Six patients with active myocarditis and one with fibrosis died.
- Extensive testing, including immunohistochemistry, in situ hybridization, and PCR, failed to identify an etiologic agent.
Implications:
- This outbreak highlights an unusual aggregation of severe pediatric myocarditis cases with a high fatality rate.
- The lack of an identified cause necessitates further investigation into potential environmental or novel infectious triggers.
- Understanding such outbreaks is crucial for improving the diagnosis and management of pediatric myocarditis.
Abstract:
The true incidence of myocarditis in children is difficult to estimate because many mild cases go undetected. This study describes an unusual cluster of myocarditis cases that occurred in young children living in the greater Baltimore area between May and October 1997. A search of multiple comprehensive databases and interviews with area pediatric cardiologists were conducted to identify unreported cases and determine the background rate of myocarditis in the area. Seven cases of myocarditis were found as well as two with a similar clinical picture and myocardial fibrosis on tissue examination. Six case patients with active myocarditis and one child with fibrosis died. The case children were predominantly black (eight of nine) and male (seven of nine), with no identifiable risk factors. The disease was characterized by a fulminant course with malignant arrhythmias. The greatest number of pediatric myocarditis deaths reported in 1 year prior to 1997 was three. Myocardial tissues were examined using immunohistochemistry, in situ hybridization, and polymerase chain reaction but no etiologic agent was identified. This outbreak is unusual because of both the number of cases and the fulminant course of the disease in this group of children.
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