A Case of Meningococcal Pericarditis Uncommon Complication of Purpura Fulminans
Published On: 14 Aug, 2025 10:59 AM | Updated On: 18 Aug, 2025 12:43 AM

A Case of Meningococcal Pericarditis Uncommon Complication of Purpura Fulminans

Abstract
Meningococcal pericarditis is a rare and potentially life-threatening complication of Neisseria meningitidis infection, typically occurring in the setting of disseminated meningococcal disease. We present a case of meningococcal pericarditis in an adult with purpura fulminans, highlighting the diagnostic challenges and need for prompt management.


Introduction
Meningococcal pericarditis is classified into three clinical types:

1.      Purulent pericarditis – due to direct bacterial invasion

2.      Immunologic pericarditis – due to immune-mediated inflammation

3.      Chronic constrictive pericarditis – a late sequela

Although Neisseria meningitidis commonly presents with meningitis or septicemia, cardiac involvement is rare. Purpura fulminans, characterized by rapidly progressive cutaneous hemorrhagic necrosis, indicates severe sepsis and carries a high mortality risk.


Case Presentation
A 32-year-old previously healthy male presented with high-grade fever, malaise, and rapidly progressive purpuric rash over the extremities. He developed hypotension and altered mental status within hours of admission.

On examination:

·         BP: 80/50 mmHg, HR: 120 bpm

·         Extensive purpura over lower limbs and trunk

·         Muffled heart sounds and distended neck veins

·         Signs of septic shock

Investigations:

·         CBC: Leukocytosis with neutrophilia

·         Coagulation profile: Prolonged PT and aPTT, low fibrinogen

·         Blood cultures: Neisseria meningitidis serogroup C

·         Echocardiography: Large pericardial effusion with early tamponade features

·         Skin biopsy: Dermal vessel thrombosis with fibrin deposition (consistent with purpura fulminans)

Management:
The patient received aggressive fluid resuscitation, broad-spectrum intravenous antibiotics (ceftriaxone), vasopressor support, and fresh frozen plasma for disseminated intravascular coagulation. Pericardiocentesis drained 500 mL of purulent fluid, which also grew N. meningitidis.

Outcome:
Despite initial stabilization, the patient required prolonged ICU stay due to multi-organ dysfunction. Over the following weeks, skin necrosis over both lower limbs necessitated surgical debridement. He was discharged after 28 days with preserved cardiac function and no evidence of constrictive physiology on follow-up echocardiography.


Discussion
Meningococcal pericarditis is rare but should be considered in patients with meningococcal septicemia who develop new cardiac symptoms or hemodynamic instability. Purpura fulminans reflects severe endotoxin-mediated vascular injury and carries a poor prognosis without rapid intervention.
Early echocardiography and timely pericardial drainage are critical to prevent tamponade-related mortality. In this case, concomitant pericardial infection and severe coagulopathy posed significant management challenges.


Conclusion
Meningococcal pericarditis, though uncommon, can complicate the course of purpura fulminans and septicemia. Clinicians should maintain a high index of suspicion for cardiac involvement in severe meningococcal disease, enabling timely diagnosis and life-saving intervention.

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