Brazilian purpuric fever

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Brazilian purpuric fever
Synonyms BPF
Pronounce N/A
Specialty N/A
Symptoms Fever, purpura, septicemia, shock
Complications Septic shock, multi-organ failure
Onset Sudden
Duration Acute
Types N/A
Causes Haemophilus influenzae biogroup aegyptius
Risks Recent conjunctivitis
Diagnosis Clinical evaluation, blood culture
Differential diagnosis Meningococcemia, Rocky Mountain spotted fever, Dengue fever
Prevention Good hygiene, prompt treatment of conjunctivitis
Treatment Antibiotics, supportive care
Medication N/A
Prognosis High mortality rate if untreated
Frequency Rare
Deaths N/A


A rare and severe illness caused by Haemophilus influenzae biogroup aegyptius


Brazilian purpuric fever (BPF) is a rare and severe illness caused by the bacterium Haemophilus influenzae biogroup aegyptius. It primarily affects children and is characterized by high fever, purpura, and septicemia. The disease was first identified in Brazil in the 1980s and has since been a subject of medical research due to its rapid progression and high mortality rate.

Etiology[edit]

BPF is caused by the bacterium Haemophilus influenzae biogroup aegyptius, which is closely related to the more common Haemophilus influenzae type b. This particular biogroup is known for its ability to cause conjunctivitis, but in the case of BPF, it leads to a more systemic and severe infection.

Pathophysiology[edit]

The pathophysiology of Brazilian purpuric fever involves the invasion of the bloodstream by H. influenzae biogroup aegyptius. The bacteria can evade the host's immune system, leading to widespread infection. The characteristic purpura seen in BPF is due to the leakage of blood into the skin and mucous membranes, a result of the vascular damage caused by the bacterial toxins.

Clinical Presentation[edit]

Patients with Brazilian purpuric fever typically present with the following symptoms:

  • High fever
  • Purpura (purple spots on the skin)
  • Conjunctivitis
  • Vomiting
  • Abdominal pain
  • Rapid progression to septicemia

The disease primarily affects children, and the rapid progression can lead to shock and death if not treated promptly.

Diagnosis[edit]

Diagnosis of BPF is based on clinical presentation and laboratory tests. Blood cultures can identify the presence of H. influenzae biogroup aegyptius. Other laboratory findings may include leukocytosis and thrombocytopenia.

Treatment[edit]

Treatment of Brazilian purpuric fever involves the use of antibiotics effective against Haemophilus influenzae. Supportive care, including fluid resuscitation and management of shock, is critical. Early intervention is essential to improve outcomes.

Prevention[edit]

Preventive measures for BPF focus on controlling the spread of H. influenzae biogroup aegyptius. This includes good hygiene practices and possibly the use of prophylactic antibiotics in close contacts of affected individuals.

Epidemiology[edit]

Brazilian purpuric fever is a rare disease, with most cases reported in Brazil. The disease primarily affects children in tropical and subtropical regions. Outbreaks have been sporadic, and the overall incidence remains low.

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