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Page 1
Evans' Syndrome: From Diagnosis to Treatment.
Audia S, Grienay N, Mounier M, Michel M, Bonnotte B. Audia S, et al. J Clin Med. 2020 Nov 27;9(12):3851. doi: 10.3390/jcm9123851. J Clin Med. 2020. PMID: 33260979 Free PMC article. Review.
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. ...
Evans' syndrome (ES) is defined as the concomitant or sequential association of warm auto-immune haemolytic anaemia (AIHA) wit …
Adult Evans' Syndrome.
Michel M. Michel M. Hematol Oncol Clin North Am. 2022 Apr;36(2):381-392. doi: 10.1016/j.hoc.2021.12.004. Epub 2022 Mar 11. Hematol Oncol Clin North Am. 2022. PMID: 35282950 Review.
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). ...
Evans syndrome (ES) is a rare immune disorder defined as the simultaneous or sequential occurrence in a single patient of immu …
Evans Syndrome.
Shaikh H, Mewawalla P. Shaikh H, et al. 2023 Jun 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Jun 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 30085557 Free Books & Documents.
The type of AIHA that presents in Evans syndrome is warm AIHA, in which IgG antibodies react with red blood cell (RBC) surface antigens at body temperature, as opposed to cold AIHA. ...Identifying Evans syndrome as secondary when associated with a dise …
The type of AIHA that presents in Evans syndrome is warm AIHA, in which IgG antibodies react with red blood cell (RBC) surface …
Paediatric-onset Evans syndrome: Breaking away from refractory immune thrombocytopenia.
Aladjidi N, Pincez T, Rieux-Laucat F, Nugent D. Aladjidi N, et al. Br J Haematol. 2023 Oct;203(1):28-35. doi: 10.1111/bjh.19073. Br J Haematol. 2023. PMID: 37735545 Review.
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. For decades, the evolution of Evans syndrome (ES) has carried a poor …
Since its first description by Evans in 1951, this syndrome has been linked to chronic immune thrombocytopenia with the concurrent or delaye …
Evans syndrome: pathology and genomic hubris.
Rao VK. Rao VK. Blood. 2022 Jan 20;139(3):312-313. doi: 10.1182/blood.2021013636. Blood. 2022. PMID: 35050333 Free PMC article. No abstract available.
Evans Syndrome.
Al Hazmi A, Winters ME. Al Hazmi A, et al. Clin Pract Cases Emerg Med. 2019 Feb 26;3(2):128-131. doi: 10.5811/cpcem.2019.1.41028. eCollection 2019 May. Clin Pract Cases Emerg Med. 2019. PMID: 31061968 Free PMC article.
He was admitted for intravenous administration of steroids, plasmapheresis, and workup of his anemia and thrombocytopenia. He was ultimately diagnosed with Evans syndrome as a presenting feature of systemic lupus erythematosus. Plasmapheresis was stopped but adminis …
He was admitted for intravenous administration of steroids, plasmapheresis, and workup of his anemia and thrombocytopenia. He was ultimately …
Naproxen-Induced Evans Syndrome.
Ahoussougbemey Mele A, Chew C, Ruiz Vega R, Mahmood R, AlRubaye R. Ahoussougbemey Mele A, et al. Cureus. 2023 Feb 13;15(2):e34910. doi: 10.7759/cureus.34910. eCollection 2023 Feb. Cureus. 2023. PMID: 36938179 Free PMC article.
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. ...This case is critical because it shines a light on one of the …
It can further be classified as primary Evans syndrome when it occurs by itself, or secondary Evans syndrome whe …
Diagnosis and management of Evans syndrome in adults: first consensus recommendations.
Fattizzo B, Marchetti M, Michel M, Cantoni S, Frederiksen H, Giordano G, Glenthøj A, González-López TJ, Murakhovskaya I, Napolitano M, Mingot ME, Arguello M, Patriarca A, Raso S, Vianelli N, Barcellini W. Fattizzo B, et al. Lancet Haematol. 2024 Aug;11(8):e617-e628. doi: 10.1016/S2352-3026(24)00144-3. Epub 2024 Jul 2. Lancet Haematol. 2024. PMID: 38968944 Review.
Evans syndrome is a rare disease marked by a severe clinical course, high relapse rate, infectious and thrombotic complications, and sometimes fatal outcome. ...These consensus-based recommendations should facilitate best practice for diagnosis and management of …
Evans syndrome is a rare disease marked by a severe clinical course, high relapse rate, infectious and thrombotic complication …
Evans Syndrome and pregnancy: A case report with literature review.
Parveen S, Mukhtar R, Shafee S, Mehmood R. Parveen S, et al. J Pak Med Assoc. 2019 Jul;69(7):1047-1048. J Pak Med Assoc. 2019. PMID: 31983745 Review.
Evans syndrome is a rare autoimmune disease in which an individual's antibodies attacks the body's own red blood cells and platelets.1 There is a coexistence of Immune thrombocytopenia (ITP) with Autoimmune haemolytic anaemia (AIHA) and both of these events may occu …
Evans syndrome is a rare autoimmune disease in which an individual's antibodies attacks the body's own red blood cells and pla …
834 results