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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.
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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.
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SUBHYALOID HEMORRHAGE IN EVANS SYNDROME
RETINAL Cases & Brief Reports, 2023Purpose: Evans syndrome is a rare disorder characterized by autoimmune hemolytic anemia and immune thrombocytopenia. We report the first case of ophthalmic involvement in a pediatric patient with Evans syndrome, in which painless vision loss was the presenting symptom.
Georges I. Guillaume +3 more
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British Journal of Haematology, 2005
SummaryEvans syndrome is an uncommon condition defined by the combination (either simultaneously or sequentially) of immune thrombocytopenia (ITP) and autoimmune haemolytic anaemia (AIHA) with a positive direct antiglobulin test (DAT) in the absence of known underlying aetiology.
Alice, Norton, Irene, Roberts
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SummaryEvans syndrome is an uncommon condition defined by the combination (either simultaneously or sequentially) of immune thrombocytopenia (ITP) and autoimmune haemolytic anaemia (AIHA) with a positive direct antiglobulin test (DAT) in the absence of known underlying aetiology.
Alice, Norton, Irene, Roberts
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The Journal of Pediatrics, 1980
The combination of idiopathic thrombocytopenic purpura and autoimmune hemolytic anemia is rare in childhood. Among 164 instances of ITP and 15 instances of AHA, 11 patients were found to have this combination. Three were found to have systemic lupus erythematosus, one had aplastic anemia, and seven had Evans syndrome.
C H, Pui, J, Wilimas, W, Wang
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The combination of idiopathic thrombocytopenic purpura and autoimmune hemolytic anemia is rare in childhood. Among 164 instances of ITP and 15 instances of AHA, 11 patients were found to have this combination. Three were found to have systemic lupus erythematosus, one had aplastic anemia, and seven had Evans syndrome.
C H, Pui, J, Wilimas, W, Wang
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Pseudohypoparathyroidism Ia With Evans Syndrome
Journal of Pediatric Hematology/Oncology, 2008Pseudohypoparathyroidism Ia (Albright hereditary osteodystrophy or Albright syndrome) is a rare disease, caused by the resistance to the action of the parathyroid hormone in target tissues, such as the bone, kidney, and intestine, with consequent hypocalcemia and hyperphosphatemia and increased levels of parathyroid hormone.
PAVONE P +3 more
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Journal of Pediatric Hematology/Oncology, 1997
Our goal was to improve the management of Evans Syndrome, an uncommon and frequently refractory condition. We conducted a retrospective survey to assess the demography, presentation, clinical course, and treatment response of affected children.Information was analyzed from a detailed questionnaire completed by pediatric hematologists mainly in the U.S.
P, Mathew, G, Chen, W, Wang
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Our goal was to improve the management of Evans Syndrome, an uncommon and frequently refractory condition. We conducted a retrospective survey to assess the demography, presentation, clinical course, and treatment response of affected children.Information was analyzed from a detailed questionnaire completed by pediatric hematologists mainly in the U.S.
P, Mathew, G, Chen, W, Wang
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Pregnancy complicated by Evan’s syndrome
European Journal of Obstetrics & Gynecology and Reproductive Biology, 2001Evan's syndrome was initially diagnosed in a 26-year-old pregnant patient. Following the introduction of high dose steroid therapy, the patient developed possible disseminated gonococcal infection which was followed by preterm labor and abruptio placentae.
Z, Selçuk Tuncer +4 more
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Laparoscopic Splenectomy for Evans Syndrome
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques, 2003Evans syndrome is a rare, chronic, sometimes fatal immunologic disorder defined as Coombs' positive hemolytic anemia and immune thrombocytopenia without an underlying etiology. This syndrome has a variable clinical course, and the benefit of splenectomy is unknown. This report reviews the clinical outcome of laparoscopic splenectomy for Evans syndrome.
Terive, Duperier +2 more
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Immunoregulatory abnormalities in evans syndrome
American Journal of Hematology, 1983AbstractImmune function in six patients with Evans syndrome (Coombs‐positive hemolytic anemia and immune thrombocytopenia) was compared to that in seven with chronic ITP. The two groups differed in measurements of T‐cell subsets and immunoglobulin production.
W, Wang +4 more
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