| Literature DB >> 25875603 |
S Caporuscio1, M L Sorgi2, S Nisticò3, G Pranteda4, U Bottoni5, I Carboni6, E Del Duca5, G Pranteda4.
Abstract
Antiphospholipid syndrome (APS) is a hypercoagulable state that leads to thrombosis and recurrent pregnancy loss related to the presence of antiphospholipid antibodies (LAC, anticardiolipin, antiA2-glycoprotein). Among cutaneous manifestations, livedo reticularis is the most frequent form of APS. In the literature, there are rare cases associated with diffuse skin necrosis (widespread skin necrosis) and intravascular thrombosis in the small vessels of the dermis. We describe the case of a 44-year-old man with positive anticardiolipin antibodies and protein S deficiency that developed scattered, bullous skin lesions, haemorrhagic in appearance with signs of necrosis as first clinical manifestation of antiphospholipid syndrome.Entities:
Keywords: antiphosholipid syndrome; intravascular thrombosis; necrosis
Mesh:
Substances:
Year: 2015 PMID: 25875603 DOI: 10.1177/0394632015582344
Source DB: PubMed Journal: Int J Immunopathol Pharmacol ISSN: 0394-6320 Impact factor: 3.219