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Hemophagocytic lymphohistiocytosis - Wikipedia
In hematology, hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic lymphohistiocytosis (British spelling), and hemophagocytic or haemophagocytic syndrome, [1] is an uncommon hematologic disorder seen more often in children than in adults.
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Lymphohistiocytosis - StatPearls - NCBI Bookshelf
2023年3月27日 · Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, hyper-inflammatory disorder affecting both newborns and adults alike. The disease is characterized by dysregulated immune activity resulting in malignant inflammation and multi-organ failure.
Recommendations for the management of hemophagocytic ...
2019年6月6日 · Hemophagocytic lymphohistiocytosis (HLH) has become more widely recognized in adults, with all ages affected. Patients often suffer from recurrent fever, cytopenia, liver dysfunction, and a sepsis-like syndrome that may rapidly progress to …
Hemophagocytic LymphoHistiocytosis (HLH) - EMCrit Project
2024年6月5日 · Causes of elevation include HLH, rheumatologic diseases involving T-cell activation, or hematologic malignancies. Overall, it's dubious what this test adds to the diagnosis of HLH. Sensitivity and specificity appear to be poor in the critical care setting. (38258680) ferritin.
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UpToDate
2022年5月6日 · Hemophagocytic lymphohistiocytosis (HLH) is a rapidly progressive, life-threatening syndrome of excessive immune activation. Prompt initiation of treatment for HLH is …
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How I treat hemophagocytic lymphohistiocytosis
2011年10月13日 · Here, we review the clinical manifestations and patterns of HLH and describe our approach to the diagnosis and therapy for this elusive and potentially lethal condition. Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation characterized by clinical signs and symptoms of extreme inflammation.