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.
Cutaneous manifestations in antiphospholipid syndrome / Caporuscio, Sara; Sorgi, Maria Laura; S., Nistico'; Pranteda, Guglielmo; Bottoni, Ugo; I., Carboni; E., Del Duca; Pranteda, Giulia. - In: INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY. - ISSN 0394-6320. - STAMPA. - 28:2(2015), pp. 270-273. [10.1177/0394632015582344]
Cutaneous manifestations in antiphospholipid syndrome
CAPORUSCIO, SARA;SORGI, Maria Laura;S. Nistico'
;PRANTEDA, Guglielmo;BOTTONI, Ugo;E. Del Duca;PRANTEDA, GIULIA
2015
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.File | Dimensione | Formato | |
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