Purpura fulminans-like lesions in antiphospholipid syndrome with endothelial C3 deposition

Jorge Magdaleno-Tapial; Cristian Valenzuela-Oñate; Javier Pitarch-Fabregat; María Marín-Jiménez; Clara Molina Almela; Johana Isidora Gutiérrez-Salcedo; Javier Calvo-Catalá; José Luis Sánchez-Carazo; V Alegre-de Miquel

doi:10.1016/j.jdcr.2018.09.006

Purpura fulminans-like lesions in antiphospholipid syndrome with endothelial C3 deposition

JAAD Case Rep. 2018 Oct 12;4(9):956-958. doi: 10.1016/j.jdcr.2018.09.006. eCollection 2018 Oct.

Authors

Jorge Magdaleno-Tapial¹, Cristian Valenzuela-Oñate¹, Javier Pitarch-Fabregat², María Marín-Jiménez³, Clara Molina Almela², Johana Isidora Gutiérrez-Salcedo⁴, Javier Calvo-Catalá², José Luis Sánchez-Carazo¹, V Alegre-de Miquel¹

Affiliations

¹ Department of Dermatology, Hospital General Universitario de Valencia, Valencia, Spain.
² Department of Rheumatology, Hospital General Universitario de Valencia, Valencia, Spain.
³ Department of Hematology, Hospital General Universitario de Valencia, Valencia, Spain.
⁴ Department of Infectious Diseases, Hospital General Universitario de Valencia, Valencia, Spain.

No abstract available

Keywords: ACL, anticardiolipin antibody; APS, antiphospholipid syndrome; DIF, direct immunofluorescent; LA, lupus anticoagulant; aPL, antiphospholipid antibodies; anti-β2GPI, anti–β2-glycoprotein antibody; anticoagulation; antiphospholipid syndrome; complement C3; purpura fulminans.

Publication types

Case Reports