| Literature DB >> 15118384 |
Alexandre Campanelli1, Gürkan Kaya, Ayse Hulya Ozsahin, Giorgio La Scala, Cédric Jacquier, Mélanie Stauffer, Françoise Boehlen, Philippe de Moerloose, Jean-Hilaire Saurat.
Abstract
Purpura fulminans is a thrombotic disease that can occur during infections, disseminated intravascular coagulation or in the context of an acquired or congenital protein C or S deficiency. Here we report the case of a 4-year-old child who developed, 5 days after a chickenpox infection, large painful ecchymotic, necrotizing and retiform plaques on the lower extremities. Laboratory analyses revealed very low protein S levels as well as anticardiolipin antibodies. Aggressive treatment by low-molecular-weight heparin, steroids, intravenous immunoglobulins and fresh frozen plasma was able to prevent the extension of the lesions and to correct the coagulation abnormalities. No lesions required skin grafting. As in our patient, an acquired protein S deficiency is probably responsible for most cases of purpura fulminans occurring after varicella, but the concomitant presence of antiphospholipid antibodies may also play a role. Copyright 2004 S. Karger AG, BaselEntities:
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Year: 2004 PMID: 15118384 DOI: 10.1159/000077315
Source DB: PubMed Journal: Dermatology ISSN: 1018-8665 Impact factor: 5.366