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Acquired purpura fulminans

Disease definition

A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans.

ORPHA:49566

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: Unknown
  • Inheritance: Not applicable 
  • Age of onset: Infancy, Neonatal, Childhood, Adult
  • ICD-10: D65
  • ICD-11: 3B20
  • OMIM: -
  • UMLS: C4510896
  • MeSH: -
  • GARD: -
  • MedDRA: 10037556

  A summary on this disease is available in Español (2014) Français (2014) Nederlands (2014) Polski ()

Additional information

Further information on this disease

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Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.