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Information Journal Paper

Title

NEONATAL PURPURA FULMINANS (CASE REPORT)

Pages

  34-37

Abstract

 Neonatal purpura fulminans is a rare and life threatening disease that can be inherited or acquired in etiology. It manifests as DIC and extensive subcutaneous thrombosis. The condition is often fatal unless there is prompt diagnosis, and judicious therapy. The most important causes of this condition are infections and congenital deficiency of anticoagulant proteins C and S.In the case of PC (PROTEIN C) deficiency, the management includes an acute phase of replacement therapy with fresh frozen plasma (FFP) or PROTEIN C concentrate and a maintenance therapy that includes anticoagulation with Warfarin or low molecular weight heparin. Here we report a case of neonatal purpura fulminans due to suspected PROTEIN C deficiency.

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    • Cite

    APA: Copy

    SAEIDI, REZA, GHARAEE, REZA, & NOBAKHT, ZOHREH. (2014). NEONATAL PURPURA FULMINANS (CASE REPORT). IRANIAN JOURNAL OF NEONATOLOGY, 5(1), 34-37. SID. https://sid.ir/paper/648910/en

    Vancouver: Copy

    SAEIDI REZA, GHARAEE REZA, NOBAKHT ZOHREH. NEONATAL PURPURA FULMINANS (CASE REPORT). IRANIAN JOURNAL OF NEONATOLOGY[Internet]. 2014;5(1):34-37. Available from: https://sid.ir/paper/648910/en

    IEEE: Copy

    REZA SAEIDI, REZA GHARAEE, and ZOHREH NOBAKHT, “NEONATAL PURPURA FULMINANS (CASE REPORT),” IRANIAN JOURNAL OF NEONATOLOGY, vol. 5, no. 1, pp. 34–37, 2014, [Online]. Available: https://sid.ir/paper/648910/en

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