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Surgical Treatment Guideline of Meningococal Induced Purpura Fulminans

Kim ES, Kim JM, Yoo SI, Noh BK, Hwang JH, Kim KS, Lee SY

  • KMID: 2203298
  • J Korean Soc Plast Reconstr Surg.
  • 2007 Jan;34(1):77-80.
PURPOSE: Purpura fulminans is a rare but rapidly progressive, serious, often life-threatening disorder in childhood, which is complicated with septic shock or disseminated intravascular coagulopathy during acute infection. It occurs...
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A case of overwhelming postsplenectomy infection with purpura fulminans by Streptococcus pneumoniae

Yoo JY, Song HG, Lee JH, Kim KS, Lee SS, Kim HJ, Chung DR

  • KMID: 2305983
  • Korean J Med.
  • 2006 Jun;70(6):725-728.
The most serious problem after splenectomy is the increased risk of life-threatening infections caused by encapsulated bacteria such as Streptococcus pneumoniae, Haemophilus influenzae, and Neisseria meningitidis. Purpura fulminans, which is...
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A Case of Streptococcal Toxic Shock Syndrome Clinically Presenting with Purpura Fulminans

Kwon HJ, Kim MY, Park YM, Kim HO, Kim YR, Kang MW

  • KMID: 1639593
  • Korean J Dermatol.
  • 2006 Mar;44(3):315-317.
Purpura fulminans is a term that describes an acute, often lethal, syndrome of hemorrhagic necrosis of the skin, due to dermal vascular thrombosis associated with vascular collapse and disseminated intravascular...
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Neonatal Purpura Fulminans Due to Homozygous Protein C Deficiency

Kim YG, Na BM, Lee GC, Kim MJ, Park HJ, Kim CY, Yoon TY

No abstract available.
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A Case of Acute Infectious Purpura Fulminans

Lee SW, Kim YC, Park HJ, Cinn YW, Yoon SC

  • KMID: 2086758
  • Korean J Dermatol.
  • 2003 Nov;41(11):1550-1553.
Purpura fulminans(PF) is a devastating disorder characterized by rapidly progressing hemorrhagic necrosis of the skin, circulatory collapse, and disseminated intravascular coagulation. Histopathologically skin lesions show thrombi within the dermal vessels,...
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A Case of Neonatal Purpura Fulminans Due to a Homozygous Protein C Deficiency

Jo JH, Oh CK, Kim MB, Jang HS, Kwon KS

  • KMID: 2146438
  • Korean J Dermatol.
  • 2002 Jan;40(1):38-43.
Homozygous protein C deficiency is a rare hereditary coagulation disorder that occurs most often in childhood and is characterized by widespread thrombosis of capillaries and venules, abrupt onset of ecchymoses...
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A Case of Purpura fulminans Caused by Streptococcus pneumoniae

Kim JS, Lee CK, Suh IB, Lee HA, Kim YK, Lee KN

  • KMID: 1892800
  • Korean J Clin Microbiol.
  • 1999 Sep;2(2):216-219.
Purpura fulminans is a potentially disabling and life-threatening disorder characterized by acute onset of progressive cutaneous hemorrhage and necrosis on distal extremities, and disseminated intravascular coagulopathy. We experienced a case...
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Purpura Fulminans

Jang KA, Koh GJ, Choi JH, Sung KJ, Moon KC, Koh JK

Purpura fulminans may be seen in three different clinical settings: (1) in the neonatal period from protein C and S deficiencies, (2) during severe bacterial infections such as “sepsis-associated” purpura...
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A Case of Neonatal Purpura Fulminans Due to Homozygous Protein C Deficiency

Choi SJ, Oh CK, Moon DC, Kwon KS, Chung TA

Homozygous Protein C deficiency is a rare genetic disease with catastrophic and fatal purpura fulminans like or thrombotic complication occurring during the neonatal period. Purpura fulminans is characterized by microvascular...
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Three cases of purpura fulminans

Suh SH, Kim HM, Yang JS, Lim BK

  • KMID: 1945953
  • J Korean Pediatr Soc.
  • 1993 May;36(5):725-732.
Purpura fulminans is one of rare consumptive coagulopathy in children. The most common predisposing conditions of purpura fulminans are infectious disease like streptococcal infection and chickenpox. This disease is characterized...
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Neonatal purpura fulminans due to homozygous protein C deficiency

Park JH, Sim SS, Kim SY, Jeon HJ, Kim CY, Oh HK, Jeong JY

  • KMID: 1691297
  • J Korean Pediatr Soc.
  • 1992 May;35(5):696-703.
No abstract available.
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A Case of Purpura Fulminans Associated with Meningococcemia

Han HK, Byun JH, Kook HI

  • KMID: 1678228
  • Korean J Dermatol.
  • 1981 Apr;19(2):239-243.
Purpura fulminans (gangrenosa) is a rare clinical syndrome characterized by sudden appearance of rapidly progressive symmetrical subcutaneous ecchymosis durimg the convalescent stage of various infectious disease. A 4 year-old. boy...
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Purpura Fulminans: Report of A Case

Chyung EJ, Cho BK, Kim JW, Houh W, Park SH, Pyun HW

  • KMID: 1678004
  • Korean J Dermatol.
  • 1980 Apr;18(2):155-159.
Purpura fuIminans is a rare form of nonthrombocytapenic purpura characterized by sudden onset, fever, prostration, anemia and symmetrical massive ecchymoses, usually of the lower extremities, and hypotension associated with disseminated...
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A case of Purpura Fulminans

Lim RK, Chung YJ, Kim CK

  • KMID: 1663473
  • J Korean Pediatr Soc.
  • 1978 Feb;21(2):156-159.
We experienced with a death by the reason of sudden development of purpura fulminans during the illness of measles in 28 months old boy, inspite of the treatment with heparin....
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