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Page 1
Purpura fulminans: recognition, diagnosis and management.
Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, Morgan M, Mumford AD. Chalmers E, et al. Arch Dis Child. 2011 Nov;96(11):1066-71. doi: 10.1136/adc.2010.199919. Epub 2011 Jan 12. Arch Dis Child. 2011. PMID: 21233082 Review.
Purpura fulminans (PF) is a haematological emergency in which there is skin necrosis and disseminated intravascular coagulation. ...
Purpura fulminans (PF) is a haematological emergency in which there is skin necrosis and disseminated intravascular coagulatio …
Purpura Fulminans.
Perera TB, Murphy-Lavoie HM. Perera TB, et al. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 30422460 Free Books & Documents.
Purpura fulminans is an acute purpuric rash characterized by coagulation of the microvasculature, which leads to purpuric lesions and skin necrosis. ...It is rapidly progressive and is often accompanied by disseminated intravascular coagulation and circulatory colla …
Purpura fulminans is an acute purpuric rash characterized by coagulation of the microvasculature, which leads to purpuric lesi …
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
Marlar RA, Neumann A. Marlar RA, et al. Semin Thromb Hemost. 1990 Oct;16(4):299-309. doi: 10.1055/s-2007-1002683. Semin Thromb Hemost. 1990. PMID: 2149204 Review.
Homozygous protein C deficiency or homozygous protein S deficiency are rare genetic diseases with catastrophic and fatal purpura fulminans-like or thrombotic complications occurring during the neonatal period. ...It is very similar to the lesions seen in idio …
Homozygous protein C deficiency or homozygous protein S deficiency are rare genetic diseases with catastrophic and fatal purpura f …
Protein C Deficiency.
Dinarvand P, Moser KA. Dinarvand P, et al. Arch Pathol Lab Med. 2019 Oct;143(10):1281-1285. doi: 10.5858/arpa.2017-0403-RS. Epub 2019 Feb 1. Arch Pathol Lab Med. 2019. PMID: 30702334 Free article. Review.
Protein C (PC) deficiency is a heritable or acquired risk factor for thrombophilia, with presentations varying from asymptomatic to venous thromboembolism to neonatal purpura fulminans, a life-threatening disorder. Hereditary PC deficiency is caused by mutati …
Protein C (PC) deficiency is a heritable or acquired risk factor for thrombophilia, with presentations varying from asymptomatic to venous t …
Diagnosis and management of neonatal purpura fulminans.
Price VE, Ledingham DL, Krümpel A, Chan AK. Price VE, et al. Semin Fetal Neonatal Med. 2011 Dec;16(6):318-22. doi: 10.1016/j.siny.2011.07.009. Epub 2011 Aug 11. Semin Fetal Neonatal Med. 2011. PMID: 21839696 Review.
Neonatal purpura fulminans is a rare, life-threatening condition, caused by congenital or acquired deficiencies of protein C or S. ...
Neonatal purpura fulminans is a rare, life-threatening condition, caused by congenital or acquired deficiencies of prot …
Acquired Versus Congenital Neonatal Purpura Fulminans: A Case Report and Literature Review.
Findley T, Patel M, Chapman J, Brown D, Duncan AF. Findley T, et al. J Pediatr Hematol Oncol. 2018 Nov;40(8):625-627. doi: 10.1097/MPH.0000000000001150. J Pediatr Hematol Oncol. 2018. PMID: 29683961 Review.
Neonatal purpura fulminans (PF) is a life-threatening disorder caused by congenital or acquired deficiencies of protein C (PC) or S. ...This case highlights the course of PF due to acquired PC deficiency in a newborn treated with PC concentrate which i …
Neonatal purpura fulminans (PF) is a life-threatening disorder caused by congenital or acquired deficiencies of protein …
Neonatal Skin Emergencies.
Siegel M, Lee LW. Siegel M, et al. Pediatr Ann. 2019 Jan 1;48(1):e36-e42. doi: 10.3928/19382359-20181210-03. Pediatr Ann. 2019. PMID: 30653641 Review.
Although the majority of neonatal skin rashes can be safely monitored without intervention, there are a significant few that are dermatologic emergencies. ...The skin may be the first clue to certain infections such as herpes simplex virus, syphilis, varicella, cytomegalov …
Although the majority of neonatal skin rashes can be safely monitored without intervention, there are a significant few that are derm …
Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency.
Gladson CL, Groncy P, Griffin JH. Gladson CL, et al. Arch Dermatol. 1987 Dec;123(12):1701a-1706a. Arch Dermatol. 1987. PMID: 2961308 Review.
Both heterozygous PC and PS deficiency appear to be inherited in an autosomal dominant manner in some families. Homozygous PC deficiency presents as neonatal purpura fulminans and results in massive venous thrombosis of the skin and other organs within the fi …
Both heterozygous PC and PS deficiency appear to be inherited in an autosomal dominant manner in some families. Homozygous PC deficiency pre …
Neonatal purpura fulminans manifestation in early-onset group B Streptococcal infection.
Albarrak M, Al-Matary A. Albarrak M, et al. Am J Case Rep. 2013 Aug 16;14:315-7. doi: 10.12659/AJCR.889352. eCollection 2013. Am J Case Rep. 2013. PMID: 23970945 Free PMC article.
PATIENT: Male, 0 FINAL DIAGNOSIS: Purpura fulminans Symptoms: Fever letargy MEDICATION: - Clinical Procedure: - Specialty: Pediatrics and Neonatology. OBJECTIVE: Rare disease. BACKGROUND: Neonatal purpura fulminans (PF) is a rare but frequently …
PATIENT: Male, 0 FINAL DIAGNOSIS: Purpura fulminans Symptoms: Fever letargy MEDICATION: - Clinical Procedure: - Specialty: Ped …
218 results