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The successful management of stroke in Evans syndrome by anticoagulation with warfarin, intravenous immunoglobulin (IVIG), and high-dose corticosteroid

open access: yesEuropean Journal of Case Reports in Internal Medicine
Evans syndrome (ES) is a rare autoimmune disorder characterised by autoimmune haemolytic anaemia (AIHA), immune thrombocytopenia and autoimmune neutropenia.
Toshiaki Takahashi   +6 more
doaj   +2 more sources

Double Trouble: The First Reported Case of Evans Syndrome Following RSV Vaccination [PDF]

open access: yesHematology Reports
Background: Evans syndrome is a rare autoimmune disease characterized by immune thrombocytopenia (ITP), autoimmune hemolytic anemia (AIHA), and autoimmune neutropenia, typically triggered by an episode of immune dysregulation or multiple other factors ...
Mohammad Abu-Tineh   +3 more
doaj   +2 more sources

Evans syndrome: clinical perspectives, biological insights and treatment modalities

open access: yesJournal of Blood Medicine, 2018
Evans syndrome (ES) is a rare and chronic autoimmune disease characterized by autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive direct anti-human globulin test.
J. Jaime-Pérez   +3 more
semanticscholar   +2 more sources

Evans syndrome suggests disease progression in lung adenocarcinoma [PDF]

open access: yesRespiratory Medicine Case Reports
We admitted a 60-year-old male patient diagnosed with lung adenocarcinoma who had a shrinking lung cancer mass after radiotherapy and 6 cycles of chemotherapy, but developed facial inflammation 2 weeks after the end of the final chemotherapy treatment ...
Shengru Yang, Xu Li, Zhang Hui
doaj   +2 more sources

Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome

open access: yesPediatric Reports, 2011
Evans Syndrome is a rare autoimmune disease consisting of hemolytic anemia, thrombocytopenia and/or neutropenia. It may be associated with other autoimmune or lymphoproliferative diseases.
Piero Farruggia   +6 more
doaj   +3 more sources

Differential diagnosis of Guillain-Barré syndrome: steroid-responsive radiculopathy in Evans syndrome [PDF]

open access: yesNeurological Research and Practice
Guillain-Barré syndrome is the most common acute inflammatory demyelinating peripheral nerve condition. Occasionally, other autoimmune conditions can mimic Guillain-Barré syndrome but may require different diagnostic workup and treatment.
Thomas Schulten   +3 more
doaj   +2 more sources

Paediatric‐onset Evans syndrome: Breaking away from refractory immune thrombocytopenia

open access: yesBritish Journal of Haematology, 2023
Since its first description by Evans in 1951, this syndrome has been linked to chronic immune thrombocytopenia with the concurrent or delayed onset of autoimmune haemolytic anaemia or neutropenia.
N. Aladjidi   +3 more
semanticscholar   +1 more source

Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndrome

open access: yesBlood Advances, 2023
Key Points • Autoimmune cytopenias are a common manifestation of IEIs.• Although IEIs often underlie pediatric Evans syndrome, no cases of IEI were identified in this real-world study of adults with ITP and Evans syndrome.
Debbie Jiang   +6 more
semanticscholar   +1 more source

Sirolimus is effective for primary refractory/relapsed warm autoimmune haemolytic anaemia/Evans syndrome: a retrospective single-center study

open access: yesAnnals medicus, 2023
Background Some patients with warm autoimmune haemolytic anaemia (wAIHA) or Evans syndrome (ES) have no response to glucocorticoid or relapse. Recent studies found that sirolimus was effective in autoimmune cytopenia with a low relapse rate. Methods Data
Zhu-Xin Zhang   +4 more
semanticscholar   +1 more source

Successful Treatment of Chidamide and Cyclosporine for Refractory/Relapsed Angioimmunoblastic T Cell Lymphoma With Evans Syndrome: A Case Report With Long-Term Follow-Up

open access: yesFrontiers in Oncology, 2020
BackgroundRefractory/relapsed angioimmunoblastic T cell lymphoma (AITL) with Evans syndrome is a very rare condition with a poor prognosis. There is no evidence-based treatment strategy for refractory/relapsed AITL with Evans syndrome.Case PresentationA ...
Fang Zhu   +8 more
doaj   +1 more source

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