Haemophagocytic lymphohistiocytosis
Hemophagocytic Lymphohistiocystosis | Johns Hopkins Medicine
Hemophagocytic lymphohistiocytosis (HLH) is a rare disease that usually occurs in infants and young children. It may also occur in adults.
Lymphohistiocytosis - StatPearls - NCBI Bookshelf
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, hyper-inflammatory disorder affecting both newborns and adults alike.
Hemophagocytic Lymphohistiocytosis: Symptoms, Causes & Outlook
Hemophagocytic Lymphohistiocytosis. Hemophagocytic lymphohistiocytosis is a rare and often life-threatening condition if left untreated. HLH ...
Hemophagocytic lymphohistiocytosis (HLH) | Immune Deficiency ...
Hemophagocytic lymphohistiocytosis (HLH) occurs when histiocytes and lymphocytes become overactive and attack the body rather than just microorganisms.
Hemophagocytic Lymphohistiocytosis (HLH) | Symptoms, Diagnosis ...
Hemophagocytic lymphohistiocytosis, also called HLH, is an immune deficiency disorder. In this type of disorder, part of the immune system is missing or ...
Lymphohistiocytosis (Hemophagocytic Lymphohistiocytosis)
Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially fatal disease of normal but overactive histiocytes and lymphocytes that ...
Hemophagocytic lymphohistiocytosis - Wikipedia
It is a life-threatening disease of severe hyperinflammation caused by uncontrolled proliferation of benign lymphocytes and macrophages that secrete high ...
Childhood Hemophagocytic Lymphohistiocytosis (HLH)
HLH is a rare but potentially fatal condition in which certain white blood cells (histiocytes and lymphocytes) build up in and damage organs.
Haemophagocytic lymphohistiocytosis: an elusive syndrome - PMC
HLH is one of the diagnostic possibilities in the undifferentiated sick adult patient who is febrile and develops cytopenias with a raised ferritin level. This ...
Hemophagocytic Lymphohistiocytosis (HLH)
Hemophagocytic lymphohistiocytosis (HLH) is a group of rare disorders of the immune system. In this disease, the immune cells grow out of control.
Clinical features and diagnosis of hemophagocytic lymphohistiocytosis
Outline · Initial presentation · Laboratory and radiographic abnormalities · - Cytopenias · - Serum ferritin levels · - Liver function and ...
Haemophagocytic lymphohistiocytosis (HLH)
Haemophagocytic lymphohistiocytosis (HLH) is a rare immune disorder where the body reacts inappropriately to a 'trigger', usually an infection.
Treatment and prognosis of hemophagocytic lymphohistiocytosis
Outline · Overview (acutely ill) · Initial HLH-specific therapy · Severe liver disease · CNS involvement · Posterior reversible encephalopathy ...
Hemophagocytic Lymphohistiocytosis - an overview | ScienceDirect ...
Hemophagocytic lymphohistiocytosis (HLH). Hemophagocytic lymphohistiocytosis (HLH) is an aggressive hyperinflammatory hematological condition often associated ...
Epidemiology, characteristics, and outcomes of adult ... - The Lancet
Haemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening syndrome characterized by an excessive inflammatory response.
Familial hemophagocytic lymphohistiocytosis - Genetics - MedlinePlus
Familial hemophagocytic lymphohistiocytosis is a disorder in which the immune system produces too many activated immune cells (lymphocytes) ...
Hemophagocytic lymphohistiocytosis: pathogenesis and treatment
HLH is a hyperinflammatory syndrome with high mortality even with appropriate treatment. This condition, which shares features with sepsis and systemic ...
Recommendations for the management of hemophagocytic ...
Hemophagocytic lymphohistiocytosis (HLH) has become more widely recognized in adults, with all ages affected. Patients often suffer from ...
Hemophagocytic Lymphohistiocytosis - Annual Reviews
Hemophagocytic lymphohistiocytosis is a life-threatening disorder characterized by unbridled activation of cytotoxic T lymphocytes, ...
Haemophagocytic lymphohistiocytosis (HLH) following allogeneic ...
Here we appraise the literature and summarise six cases of sHLH following adult HSCT over a 5-year period (2014–18), suggesting sHLH is an under-recognised ...