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Acute and Chronic Q Fever in a Child With Repaired Tetralogy of Fallot: A Case Report
Alaa Mohammed Al Juaid1, Faisal Almalki2, Reema E Aloteibi2
1Pediatrics, King Abdullah Specialized Children Hospital, Ministry of National Guard - Health Affairs, Jeddah, SAU.
Insights
Q fever can present as a serious illness in children, especially those with congenital heart disease. Early diagnosis and long-term antibiotic treatment are crucial for recovery.
Area of Science:
- Pediatric Infectious Diseases
- Cardiology
- Medical Case Reports
Background:
- Q fever (Coxiella burnetii infection) typically presents as acute febrile illness in children.
- Congenital heart disease (CHD) can complicate presentations and management of infections.
Observation:
- A 38-month-old girl with complex CHD (tetralogy of Fallot, pulmonary atresia, VSD) presented with fever, dyspnea, and vomiting.
- Initial treatment for pneumonia was ineffective; patient developed heart failure, hepatosplenomegaly, and pancytopenia.
Findings:
- Positive Q fever serology confirmed chronic Q fever.
- 18-month treatment with doxycycline and hydroxychloroquine led to improved liver function and normalized echocardiography within four months.
Implications:
- Highlights the importance of considering Q fever in pediatric patients with complex CHD.
- Emphasizes the need for comprehensive diagnostic workup and prolonged antibiotic therapy for chronic Q fever.
- Underscores the potential for Q fever to cause severe systemic illness in immunocompromised or complex cardiac pediatric patients.
Abstract:
In children, Q fever often presents as an acute febrile illness, sometimes with pneumonia or hepatitis. We report in this case a 38-month-old girl with complex congenital heart disease (tetralogy of Fallot, pulmonary atresia, and ventricular septal defect) who presented with a four-day history of fever, shortness of breath, and vomiting. She had prior cardiac interventions. After admission to the PICU, she was initially treated for severe pneumonia. During her stay, her condition worsened with heart failure, hepatosplenomegaly, and pancytopenia. After extensive investigations, Q fever serology was positive, indicating chronic Q fever. The patient was treated with doxycycline and hydroxychloroquine for 18 months. Her liver function improved, and echocardiography was normal after four months. This case highlights the importance of considering Q fever in pediatric patients with cardiac history, the need for comprehensive investigations, and appropriate long-term antibiotic treatment.
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