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Acute infectious purpura fulminans associated with asplenism or hyposplenism
Kimberley Morine Ward1, Julide Tok Celebi, Robyn Gmyrek
1Department of Dermatology, Columbia University, The New York Presbyterian Hospital, New York, USA.
Abstract:
Acute infectious purpura fulminans is a rapidly progressive syndrome of hemorrhagic skin necrosis associated with acute infection and disseminated intravascular coagulation. We report 5 cases of purpura fulminans and briefly review the literature. All cases were associated with encapsulated organisms (Streptococcus pneumoniae or Group A streptococcus), and 4 of the 5 patients had asplenism or functional hyposplenism.
Insights
Acute infectious purpura fulminans, a severe skin necrosis syndrome, is linked to bacterial infections and blood clotting issues. Encapsulated bacteria like Streptococcus pneumoniae were common in patients, especially those with spleen dysfunction.
Area of Science:
- Infectious Diseases
- Hematology
- Dermatology
Background:
- Purpura fulminans is a rare, life-threatening condition characterized by widespread purpura and hemorrhagic necrosis.
- It is often associated with severe bacterial infections and disseminated intravascular coagulation (DIC).
Observation:
- This report details five cases of acute infectious purpura fulminans.
- All identified cases were linked to encapsulated bacterial pathogens, specifically Streptococcus pneumoniae and Group A Streptococcus.
Findings:
- Four out of five patients presented with asplenism or functional hyposplenism.
- The syndrome involves rapid progression of skin necrosis and DIC.
Implications:
- Early recognition and prompt treatment are crucial for managing purpura fulminans.
- Understanding the association with encapsulated organisms and splenic function is vital for risk stratification and prevention strategies.
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