Acute kidney injury in critical care: complications of hemophagocytic lymphohistiocytosis
M Zhao, Y Guan, J Lin, Y Qiu, S Zhao… - Frontiers in …, 2024 - frontiersin.org
Hemophagocytic lymphohistiocytosis (HLH) is an immune dysfunction characterized by an
exaggerated and pathological inflammatory response, potentially leading to systemic …
exaggerated and pathological inflammatory response, potentially leading to systemic …
Tuberculosis-associated hemophagocytic lymphohistiocytosis: diagnostic challenges and determinants of outcome
L Kurver, T Seers, S van Dorp… - Open Forum …, 2024 - academic.oup.com
Background Tuberculosis (TB) can induce secondary hemophagocytic lymphohistiocytosis
(HLH), a severe inflammatory syndrome with high mortality. We integrated all published …
(HLH), a severe inflammatory syndrome with high mortality. We integrated all published …
Idiopathic multicentric Castleman disease-TAFRO results in high levels of mTOR activator SVEP1, tissue factor, and endotheliopathy
C Lossos, J Brown, S Sheikhbahaei… - Blood Vessels …, 2024 - ashpublications.org
Idiopathic multicentric Castleman disease (iMCD) is an inflammatory disease associated
with a cytokine storm, activation of the PI3K/AKT/mTOR pathway, coagulopathy, and …
with a cytokine storm, activation of the PI3K/AKT/mTOR pathway, coagulopathy, and …
[引用][C] Secondary haemophagocytic lymphohistiocytosis: time for a united approach to diagnosis and cytokine blockade
L Flower, JJ Manson - Anaesthesia Reports, 2024 - Wiley Online Library