Results 21 to 30 of about 625 (114)
Extreme Hyperferritinemia: Causes and Prognosis
The significance of extreme hyperferritinemia and its association with certain diagnoses and prognoses are not well characterized. We performed a retrospective analysis of adult patients with at least one total serum ferritin (TSF) measurement ≥ 5000 µg/L over 2 years, in three university hospitals.
Fauter, Maxime +8 more
openaire +3 more sources
Ferritin in Adult-Onset Still’s Disease: Just a Useful Innocent Bystander?
Background. Adult-Onset Still’s Disease (AOSD) is an immune-mediated systemic disease with quotidian-spiking fever, rash, and inflammatory arthritis. Hyperferritinemia is a prominent feature, often used for screening. Methods.
Bella Mehta, Petros Efthimiou
doaj +1 more source
Kumachev, Alexander, Frost, David W.
openaire +4 more sources
Background Mucormycosis is a serious fungal infection associated with uncontrolled diabetes and immunocompromised patients. This angioinvasive infection emerged as a post‐covid complication worldwide especially in developing countries.
Ayesha Irfan +3 more
doaj +1 more source
Extreme Hyperferritinemia [PDF]
Hyperferritinemia can be a result of inflammation, infection, chronic iron overload, or other uncommon pathologies including hemophagocytic lymphohistiocytosis (HLH). There is a historical association between extreme hyperferritinemia and HLH, but in reality HLH is associated with a minority of hyperferritinemic states.We identified conditions most ...
Katie, Sackett +4 more
openaire +2 more sources
Ferritin as a biomarker of infection in COVID-19 non-hospitalized patients [PDF]
Background: Serum ferritin is an iron storage protein with a primary role of regulating cellular oxygen metabolism, Ferritin has emerged as a key in the immune system, and its role as an acute phase reactant, recent studies have focused on the role of ...
Ahmed Yameny
doaj +1 more source
A child with hyperferritinemia: Case report [PDF]
Abstract Hereditary hyperferritinemia cataract syndrome (HHCS) is a rare condition caused by mutations in the gene coding for the light chain of ferritin; it does not lead to iron overload, but it is associated with the risk of developing a bilateral nuclear cataract also in childhood.
M. Serra +4 more
openaire +3 more sources
Clinical case of hemophagocytic lymphohistiocytosis: rare or undiagnosed syndrome?
Hemophagocytic lymphohistiocytosis (hemophagocytic syndrome, HLH) is a life-threatening hyperinflammatory condition associated with a high mortality rate; it is characterized by hyperstimulation of histiocytes and cytotoxic T-cells, which leads to ...
O. B. Yaremenko +2 more
doaj +1 more source
Adult-Onset Still's Disease: A Rare Cause of Pyrexia of Unknown Origin (Case Report with Literature Review) [PDF]
Adult-onset Still’s disease (AOSD) is a remarkably rare illness. One well-known pathogenic process that results in systemic manifestations is auto-inflammatory disease.
Bushra Ali +5 more
doaj +1 more source
Hyperferritinemia and COVID-19?
Poznato je da je povećana koncentracija feritina u serumu ili hiperferitinemija povezana s COVID-19, posebno u težim oblicima ove bolesti. Feritin je molekula čija se koncentracija određuje kao biljeg koji odražava opskrbu organizma sa željezom, te manje značajno kao biljeg upale infektivnog i neinfektivnog podrijetla. Ekspresija ove molekule neophodne
Čepelak, Ivana +2 more
openaire +6 more sources

