Table 1.

Classification of purpura fulminans

InheritedAutoimmune or postinfectious (“idiopathic”)Acute infectious
Mechanism Inherited PC or rarely PS deficiency Neutralizing antibodies against PS or rarely PC Aberrant tissue factor expression with concomitant failure of thrombomodulin-PC system 
Associations  • Varicella zoster virus
• Human herpesvirus 6 
• Neisseria meningitidis
• Haemophilus influenza
• Streptococcus pneumoniae
• Other encapsulated organisms
• Staphylococcus aureus
• Capnocytophaga canimorsus
• Rickettsial infection
• Plasmodium falciparum 
Clinical setting Neonatal Within 2 weeks after viral infection Septic shock 
Rash distribution Lower half of body > upper half Lower half of body > upper half Distal to proximal progression (worse in acral areas) or diffuse from onset 
Laboratory findings • Thrombocytopenia
• Elevated D-dimer or fibrin split products
• Hypofibrinogenemia
• Prolonged PT and/or aPTT
• Low PC, PS, and antithrombin activity 
InheritedAutoimmune or postinfectious (“idiopathic”)Acute infectious
Mechanism Inherited PC or rarely PS deficiency Neutralizing antibodies against PS or rarely PC Aberrant tissue factor expression with concomitant failure of thrombomodulin-PC system 
Associations  • Varicella zoster virus
• Human herpesvirus 6 
• Neisseria meningitidis
• Haemophilus influenza
• Streptococcus pneumoniae
• Other encapsulated organisms
• Staphylococcus aureus
• Capnocytophaga canimorsus
• Rickettsial infection
• Plasmodium falciparum 
Clinical setting Neonatal Within 2 weeks after viral infection Septic shock 
Rash distribution Lower half of body > upper half Lower half of body > upper half Distal to proximal progression (worse in acral areas) or diffuse from onset 
Laboratory findings • Thrombocytopenia
• Elevated D-dimer or fibrin split products
• Hypofibrinogenemia
• Prolonged PT and/or aPTT
• Low PC, PS, and antithrombin activity 

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