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Evans Syndrome: A Case Report [PDF]
Journal of Nepal Medical Association, 2022 Evans syndrome is defined as the concomitant or sequential association of warm autoimmune hemolytic anaemia with immune thrombocytopenia, and less frequently autoimmune neutropenia.
Sanam Dhakal +4 more
doaj +4 more sources
Clinical Practice and Cases in Emergency Medicine, 2019 A 22-year-old man presented to the emergency department with facial swelling, rash, and fatigue. He had a past medical history of pericarditis and pericardial effusion. His evaluation showed anemia and thrombocytopenia.
Ahmed Al Hazmi, Michael E. Winters
doaj +4 more sources
The Pan African Medical Journal, 2021 This manuscript concerns the case of a patient hospitalized and diagnosed with Evans syndrome. She was hospitalized with signs of thrombocytopenia induced purpura, petechiae, ecchymosis and anemia.
Andreas Angelopoulos +3 more
doaj +4 more sources
Case Report: Native aortic valve Listeria monocytogenes endocarditis in an adult with Evans syndrome [PDF]
Frontiers in ImmunologyBackgroundListeria monocytogenes is an uncommon cause of infective endocarditis but is associated with a high morbidity and mortality rate in immunocompromised hosts.
Chen-Yu Wei +10 more
doaj +2 more sources
Anti-CD19 chimeric antigen receptor T cells in Evans syndrome of systemic lupus erythematosus [PDF]
Annals of HematologyEvans syndrome, characterized by autoimmune hemolytic anemia and immune thrombocytopenia, is rare and often refractory to conventional therapies. In Chinese patients with systemic lupus erythematosus (SLE), its incidence is approximately 0.47%. We report
Min Lang +6 more
doaj +2 more sources
Naproxen-Induced Evans Syndrome. [PDF]
Cureus, 2023 Evans syndrome is an autoimmune disorder characterized by the simultaneous occurrence of autoimmune hemolytic anemia and immune thrombocytopenic purpura. It can further be classified as primary Evans syndrome when it occurs by itself, or secondary Evans syndrome when it is associated with other autoimmune and lymphoproliferative disorders ...
Ahoussougbemey Mele A +4 more
europepmc +3 more sources
Severe relapse of Evans syndrome in an adult patient with treatment resistance and fatal outcome: A case report [PDF]
Journal of International Medical ResearchEvans syndrome is an uncommon autoimmune disorder characterized by autoimmune hemolytic anemia and immune thrombocytopenia. It can follow a relapsing course in adults and may be challenging to treat.
Amr R Saleh +3 more
doaj +2 more sources
Evans syndrome during pembrolizumab therapy for upper urinary tract cancer [PDF]
IJU Case Reports, 2023 Introduction Immune checkpoint inhibitors are available for the treatment of advanced urothelial carcinoma; however, serious adverse events occasionally occur.
Shota Kakita +8 more
doaj +2 more sources
La Pediatria Medica e Chirurgica, 2014 We describe a case of a 14-years old caucasian female affected by autoimmune hemolytic anemia and thrombocytopenia successfully treated with intravenous immunoglobulin and steroids. Nevertheless, neutropenia occurred during follow-up period.
F. Porcaro +9 more
doaj +5 more sources
Evans syndrome as a presentation in systemic lupus erythematous, coexisting with Hashimoto’s thyroiditis and pernicious anemia: a case report [PDF]
Journal of Medical Case ReportsBackground Evans syndrome is a rare disorder characterized by the simultaneous or sequential combination of autoimmune hemolytic anemia and immunological thrombocytopenia, together with a positive direct antiglobulin test.
Maryam Mansour +4 more
doaj +2 more sources