Evans syndrome suggests disease progression in lung adenocarcinoma [PDF]
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]
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
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]
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]
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
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
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]
M. Almakadi, D. Aldhafeeri
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Surfactant protein D contributes to ocular defense against Pseudomonas aeruginosa in a murine model of dry eye disease. [PDF]
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.
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

