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Published on: July 14, 2020
A Rare Case of Pediatric Infective Endocarditis Initially Presenting as Meningitis in a Previously Healthy Child
Tuqa A Abdulsalam1, Farheen Khan2, Haytham Hussein3
1General Pediatrics, Al Jalila Children's Hospital, Sharjah, ARE.
Insights
Infective endocarditis in children can be life-threatening, even without prior heart disease. Early surgical intervention and multidisciplinary care are crucial for successful outcomes in complex pediatric cases.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Critical Care Medicine
Background:
- Infective endocarditis (IE) is a rare but severe condition in children, posing significant risks especially in those without pre-existing cardiac conditions.
- Delayed diagnosis of pediatric IE can result in severe systemic complications, increasing morbidity and mortality.
Observation:
- A previously healthy eight-year-old girl was initially misdiagnosed with bacterial meningitis.
- Despite antibiotic treatment, she developed multiple septic embolic events, including cerebral, splenic, and renal infarctions, and digital gangrene.
- Serial echocardiograms identified mitral valve vegetation and an aortic root abscess, with blood cultures confirming methicillin-sensitive Staphylococcus aureus (MSSA).
Findings:
- The patient underwent successful surgical management using a modified Ross procedure.
- A six-week course of intravenous flucloxacillin contributed to her full recovery.
- The case highlights the diagnostic challenges associated with pediatric IE in healthy children.
Implications:
- This case emphasizes the importance of considering IE in pediatric patients presenting with non-specific symptoms, even without cardiac risk factors.
- Serial imaging, prompt multidisciplinary collaboration, and timely surgical intervention are critical for managing pediatric infective endocarditis.
- Successful treatment underscores the effectiveness of combined surgical and antibiotic approaches in complex pediatric IE cases.
Abstract:
Infective endocarditis (IE) is a rare but life-threatening condition in children, particularly in those without heart disease. Delayed diagnosis can lead to serious systemic complications. We report the case of an eight-year-old previously healthy girl, initially misdiagnosed with bacterial meningitis, who developed multiple septic embolic events (cerebral infarcts, digital gangrene, and splenic and renal infarction) despite being on antibiotic therapy. Repeat echocardiograms revealed mitral valve vegetation and an aortic root abscess. Blood cultures (aerobic and anaerobic) grew methicillin-sensitive Staphylococcus aureus (MSSA). She underwent successful surgical management via a modified Ross procedure, followed by a six-week course of intravenous (IV) flucloxacillin, resulting in full recovery. This case underscores the diagnostic challenges of pediatric IE in patients without known cardiac risk factors and highlights the critical role of serial imaging, multidisciplinary care, and early surgical intervention in achieving favorable outcomes.
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