- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Neonatal Purpura Fulminans Due to Homozygous Protein C Deficiency
-
Choi SJ, Oh CK, Moon DC, Kwon KS, Chung TA
- KMID: 2361483
- Ann Dermatol.
- 1994 Jan;6(1):63-68.
- doi: 10.5021/ad.1994.6.1.63
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... -
- CITED
-
- Close
- SHARE
-
- Close
- Purpura Fulminans
-
Jang KA, Koh GJ, Choi JH, Sung KJ, Moon KC, Koh JK
- KMID: 2359735
- Ann Dermatol.
- 1999 Apr;11(2):75-77.
- doi: 10.5021/ad.1999.11.2.75
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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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. -
- CITED
-
- Close
- SHARE
-
- Close
- 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.... -
- CITED
-
- Close
- SHARE
-
- Close
- Neonatal Purpura Fulminans Due to Homozygous Protein C Deficiency
-
Kim YG, Na BM, Lee GC, Kim MJ, Park HJ, Kim CY, Yoon TY
- KMID: 2158541
- Ann Dermatol.
- 2004 Dec;16(4):176-179.
- doi: 10.5021/ad.2004.16.4.176
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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,... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Meningococcal Infection necessitating Amputation of Both Legs in a Child
-
Shin HJ, Lee BY, Choe BK, Kim CS, Kim HS, Song KS, Kim HJ, Lee HJ
- KMID: 1528888
- Infect Chemother.
- 2007 Aug;39(4):222-225.
Meningococcal sepsis-associated purpura fulminans is a rapidly progressing condition with high morbidity and mortality. There are several reports of amputation of extremities due to gangrenous change in this condition. However,... -
- CITED
-
- Close
- SHARE
-
- Close
- 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... -
- CITED
-
- Close
- SHARE
-
- Close
- Cerebral Palsy due to Intracranial Hemorrhage Caused by Consumptive Coagulopathy in Protein C Deficiency: A Case Report
-
Cho Y, Lee YM, Park ES, Choi JY, Park C, Rha DW
- KMID: 2385213
- J Korean Child Neurol Soc.
- 2017 Mar;25(1):44-47.
- doi: 10.0000/jkcns.2017.25.1.44
Protein C (PROC) is a potent anticoagulant inactivating coagulation factors Va and VIIIa. PROC deficiency is very rare condition inherited as an autosomal dominant or recessive trait, and associated with... -
- CITED
-
- Close
- SHARE
-
- Close
- Diagnosis of Severe Protein C Deficiency Confirmed by Presence of Rare PROC Gene Mutation
-
Lim MS, Shin JE, Lee SM, Eun HS, Park MS, Park KI, Namgung R, Lee KA, Lee JS
- KMID: 2360464
- Neonatal Med.
- 2016 Nov;23(4):233-237.
- doi: 10.5385/nm.2016.23.4.233
Protein C (PROC) deficiency is caused by mutations in the PROC gene on chromosome 2q14.3. Patients with PROC deficiency typically present distinguished purpura, intracerebral and intravascular coagulopathy, and ophthalmologic complications.... -
- CITED
-
- Close
- SHARE
-
- Close
- Anesthesia for Living Related Liver Transplantation in Homozygous Protein C Deficiency
-
Cheong MA, Hwang KS, Choi KT, Choi Y, Lee EJ, Chung EJ
- KMID: 2091627
- Korean J Anesthesiol.
- 2001 May;40(5):671-676.
- doi: 10.4097/kjae.2001.40.5.671
Protein C exerts anticoagulant effects by inactivating factor Va and VIIIa and stimulating fibrinolysis. The homozygous protein C deficiency is extremely rare and often results in life threatening thrombosis and... -
- CITED
-
- Close
- SHARE
-
- Close
