Results 1 to 10 of about 4,455,205 (312)
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
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 +3 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
Evans syndrome during pembrolizumab therapy for upper urinary tract cancer
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
Hematology/Oncology Clinics of North America, 2022 Evans syndrome (ES) is a rare immune disorder defined as the simultaneous or sequential occurrence in a single patient of immune thrombocytopenia (ITP) and warm autoimmune hemolytic anemia (wAIHA) ± autoimmune neutropenia (AIN). ES represents approximately 5% to 10% of all wAIHA and 2%-5% of all ITP cases in adults and its mortality rate is high.
M. Michel
openaire +3 more sources
Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia
Frontiers in Pediatrics, 2023 Kabuki syndrome (KS) is a rare multisystemic disease due to mutations in the KMT2D or KDM6A genes, which act as epigenetic modulators of different processes, including immune response. The syndrome is characterized by anomalies in multiple organ systems,
Luigi Tarani +2 more
exaly +2 more sources
Concurrent severe pulmonary tuberculosis with Evans syndrome: a case report with literature review
BMC Infectious Diseases, 2022 Background Tuberculosis is a bacterial infection involving multiple organs and systems. Its hematological presentation mainly includes anemia and leukocytosis.
Xiao-hong Pan +7 more
doaj +2 more sources
Evans’ Syndrome: From Diagnosis to Treatment
Journal of Clinical Medicine, 2020 Evans’ syndrome (ES) is defined as the concomitant or sequential association of warm auto-immune haemolytic anaemia (AIHA) with immune thrombocytopenia (ITP), and less frequently autoimmune neutropenia.
Bernard Bonnotte +2 more
exaly +2 more sources
Fulminant Evans syndrome and splenic infarction as initial manifestations of POEMS syndrome with monoclonal kappa light chain restriction: a diagnostic and therapeutic challenge [PDF]
European Journal of Case Reports in Internal MedicineIntroduction: Autoimmune cytopenias have been very rarely reported in conjunction with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome).
Mohamed Reda Belkhribchia +6 more
doaj +2 more sources