Results 11 to 20 of about 303,442 (283)

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

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

Experience with Evans syndrome in an academic referral center

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2015
OBJECTIVE: To document the experience of one referral service with patients diagnosed with Evans syndrome, the treatment and response and to briefly review current treatment strategies and results.METHODS: Patients enrolled in this study fulfilled ...
José Carlos Jaime-Pérez   +4 more
doaj   +3 more sources

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

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

Evans’ syndrome in an old patient: case presentation [PDF]

open access: yesArchives of the Balkan Medical Union, 2019
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

Síndrome de Evans - presentación atípica de un linfoma raro

open access: yesGalicia Clínica, 2022
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

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

PB2293: HARNESSING ACCELERATED SEQUENTIAL EVANS SYNDROME [PDF]

open access: yesHemaSphere, 2022
M. Almakadi, D. Aldhafeeri
doaj   +2 more sources

Surfactant protein D contributes to ocular defense against Pseudomonas aeruginosa in a murine model of dry eye disease. [PDF]

open access: yes, 2013
Dry eye disease can cause ocular surface inflammation that disrupts the corneal epithelial barrier. While dry eye patients are known to have an increased risk of corneal infection, it is not known whether there is a direct causal relationship between ...
Evans, David   +4 more
core   +6 more sources

Evans syndrome in children below 13 years of age - A nationwide population-based cohort study.

open access: yesPLoS ONE, 2020
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

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