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Síndrome de Evans - presentación atípica de un linfoma raro
Evans Syndrome is a rare autoimmune condition characterized by two or more cytopenias, usually autoimmune haemolytic anaemia and immune thrombocytopenic purpura. It can be primary/idiopathic or secondary to other diseases.
Catarina Teles Neto +5 more
doaj +1 more source
Evans’ syndrome in an old patient: case presentation [PDF]
Introduction. Evans’ syndrome (autoimmune hemolytic anemia combined with thrombocytopenia) is a rare hematological syndrome in the elderly. Case report. A 94-year-old patient was diagnosed with Evans’ syndrome with the secretion of monoclonal protein.
Leonid I. DVORETSKY +3 more
doaj +1 more source
The spectrum of Evans' syndrome [PDF]
Eleven patients (10 boys, one girl) with Evans' syndrome with a median follow up time of 8.0 years were evaluated retrospectively. Six patients had either persistent hepatosplenomegaly or generalised lymphadenopathy, or both. In five patients, an increase in lymph node and/or spleen size was observed during the exacerbations of cytopenias.
S, Savaşan, I, Warrier, Y, Ravindranath
openaire +2 more sources
Secondary Fisher–Evans syndrome in a child with activated PI(3)kd syndrome and lymphoma
Evans syndrome, a combination of autoimmune hemolytic anemia and immune thrombocytopenia, is a rare disease in children. In childhood, it may turn out to be one of the first manifestations of a primary immunodeficiency or an immune dysregulation syndrome.
Z. Kuzminova +7 more
semanticscholar +1 more source
Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3
Increasing evidence suggests multilineage cytopenias (also known as Evans syndrome) may be caused by inborn errors of immunity (IEI) with immune dysregulation.
W. Novak +15 more
semanticscholar +1 more source
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel +93 more
wiley +1 more source
Evans syndrome in children below 13 years of age - A nationwide population-based cohort study.
Evans syndrome is defined by autoimmune haemolytic anaemia and immune thrombocytopenia occurring in the same patient. Although known to be rare the frequency and prognosis of Evans syndrome in children is unknown, and only few registry-based studies are ...
Nikolaj Mannering +2 more
doaj +1 more source
Evans Syndrome and Hashimoto's Thyroiditis in Pregnancy: A Case Report
Evans syndrome is a combination of autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura. Evans syndrome is a rare disease encountered in medical practice. Evans syndrome can also co-occur with other autoimmune diseases, such as Hashimoto's
Marcella Adisuhanto +7 more
semanticscholar +1 more source
Challenges of providing biochemistry results in a patient with Evans syndrome
Highlights A case report of in vivo hemolysis in patient with Evans syndrome is described Hemolysis disrupts biochemistry analysis, yielding unreliable results A laboratory designed algorithm ensures results with interpretative comments Close ...
Natividad Rico Ríos +5 more
semanticscholar +1 more source
Evans Syndrome in a Jehovah’s Witness [PDF]
Evans syndrome (ES) is a rare hematologic disorder characterized by the development of autoimmune hemolytic anemia (AIHA), idiopathic thrombocytopenia, and occasionally immune-mediated neutropenia. Jehovah's Witnesses (JW) often decline blood product transfusion on the grounds of a scriptural stand based on biblical texts.
Leonhardt, Lex P +2 more
openaire +2 more sources

