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Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature
Alina Bhat1, Elvira Neculiseanu1, Eric L Tam1
1a Downstate College of Medicine, Department of Medicine, Division of Hematology-Oncology , State University of New York , Brooklyn , NY , USA.
Abstract:
Purulent pericarditis is a localized infection with a thick, fibrinous hypercellular exudate and is historically associated with a high mortality. We describe a case of purulent pericarditis due to Streptococcus agalactiae (S. agalactiae) in a 30-year-old woman with sickle cell disease who presented with fever, dyspnea, and S. agalactiae septicemia. Despite timely initiation of antibiotics, she developed a large purulent pericardial effusion requiring surgical pericardiocentesis followed by a pericardial window. At 14 months follow-up, she has remained asymptomatic without sequelae. A review of the literature contained only four patients with purulent pericarditis in sickle cell patients. We discuss the unique aspects of this case in the context of purulent pericarditis in the age of modern antibiotics and hypothesize on the pathogenesis of delayed pericardial effusion after pericarditis.
Insights
Purulent pericarditis caused by Streptococcus agalactiae is rare in sickle cell disease patients. This case highlights the need for prompt surgical intervention and surgical pericardiocentesis for effective management.
Area of Science:
- Infectious Diseases
- Cardiology
- Hematology
Background:
- Purulent pericarditis, characterized by a thick exudate, historically carries a high mortality rate.
- Streptococcus agalactiae (S. agalactiae) is an uncommon cause of purulent pericarditis, particularly in patients with underlying conditions like sickle cell disease.
Observation:
- A 30-year-old woman with sickle cell disease presented with fever, dyspnea, and S. agalactiae septicemia, indicative of a severe infection.
- Despite prompt antibiotic treatment, she developed a significant purulent pericardial effusion, necessitating surgical intervention.
Findings:
- The patient underwent surgical pericardiocentesis and a pericardial window procedure for the large purulent pericardial effusion.
- Literature review revealed only four previously reported cases of purulent pericarditis in sickle cell patients, underscoring the rarity of this presentation.
Implications:
- This case emphasizes the importance of considering purulent pericarditis in sickle cell patients presenting with sepsis and respiratory symptoms.
- The successful surgical management highlights its critical role in improving outcomes for this rare and potentially fatal condition.
- Further research into the pathogenesis of delayed pericardial effusion in purulent pericarditis is warranted.
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