Adult-onset Still's disease: Evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers [PDF]
, 2016 Background: Adult-onset Still's disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes ...
Berardicurti O. +13 more
core +1 more source
Antiphospholipid syndrome: A review
Journal of Mahatma Gandhi Institute of Medical Sciences, 2014 Antiphospholipid syndrome is being increasingly recognized as a disease with a myriad of clinical manifestations ranging from recurrent thrombosis and pregnancy morbidity to valvular lesions, transverse myelitis, thrombocytopenia and hemolytic anemia. It
Varun Dhir, Benzeeta Pinto
doaj +1 more source
Direct Oral Anticoagulants for Thromboprophylaxis in Patients with Antiphospholipid Syndrome [PDF]
, 2018 The current mainstay of the treatment and secondary thromboprophylaxis of thrombotic antiphospholipid syndrome (APS) is anticoagulation with warfarin or other vitamin K antagonists (VKAs).
Cohen, H +3 more
core
Catastrophic Antiphospholipid Syndrome [PDF]
, 2020 INTRODUCTION: Catastrophic Antiphospholipid Syndrome (CAPS) is a rare and extreme manifestation of Antiphospholipid Syndrome (APS) that features widespread thrombotic disease affecting multiple small vessels in a short time frame.
Hocum, Gabriel, Youker, Jeff
core +1 more source
Catastrophic antiphospholipid antibody Syndrome [PDF]
American Journal of Hematology, 2003 Stephan, Moll +2 more
openaire +2 more sources
Plasma Exchange in the Management of Catastrophic Antiphospholipid Syndrome
Case Reports in Critical Care, 2016 Objective. Report of a case of catastrophic antiphospholipid syndrome (CAPS) with multiple organ involvement leading to a life-threatening condition despite early combination corticosteroid and heparin therapy.
Dimitri Titeca-Beauport +4 more
doaj +1 more source
Childhood-onset systemic lupus erythematosus in Croatia: demographic, clinical and laboratory features, and factors influencing time to diagnosis [PDF]
, 2013 OBJECTIVES Childhood-onset systemic lupus erythematosus (cSLE) presents with diverse clinical features and often with non-classical symptoms that may delay diagnosis and increase risk of morbidity and mortality.
Batinić, Danica +10 more
core
Significance of global versus segmental subclassification of class III and IV lupus nephritis: a single center experience [PDF]
, 2015 Introduction: Class III and IV are the most ominous among the classes of lupus nephritis (LN) and there are contradictory reports on whether LN class IV-G (global) differs from LN class IV-S (segmental), as envisaged by the International Society of ...
Baradaran, Azar. +3 more
core +1 more source
Calcifilaxia: Revisão da Literatura a Propósito de 2 Casos Clínicos [PDF]
, 2014 Calciphylaxis is a rare and devastating obliterative vasculopathy, leading to ischemia and subcutaneous necrosis. In most cases it affects patients with renal disease and is associated with high morbidity and mortality.
Ferreira, A +3 more
core