Results 201 to 210 of about 22,345 (254)
Post-streptococcal Hemophagocytic Lymphohistiocytosis in an Immunocompetent Adult. [PDF]
CureusKeramane HZ +4 more
europepmc +1 more source
Refractory Autoimmune Hemophagocytic Lymphohistiocytosis in Adults: Multi-therapy Failure and the Limits of Salvage Transplantation. [PDF]
CureusAlmaalouli B +4 more
europepmc +1 more source
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HLH Associated with Disseminated Tuberculosis
New England Journal of Medicine, 2020HLH Associated with Disseminated Tuberculosis A 63-year-old man presented with fever, dyspnea, and weight loss. Bone marrow biopsy revealed hemophagocytosis and noncaseating granulomas.
Michael, Kessler, Erica, Reinig
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Inpatient recognition and management of HLH
Hematology, 2023Abstract Hemophagocytic lymphohistiocytosis (HLH) is one of the life-threatening emergencies that a hematologist may be called upon to diagnose and manage. It is a hyperinflammatory process that develops in patients with genetic abnormalities, hematologic malignancies, chronic inflammatory states, or infections.
Adi, Zoref-Lorenz +2 more
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SAE Technical Paper Series, 1979
<div class="htmlview paragraph">Design, fabrication, and test of large high powered helicopter components in the U.S. Army Heavy Lift Helicopter Advanced Technology Component development program demonstrated the feasibility of efficient, large helicopter components and reduced the risk and cost of future heavy lift helicopter development.
Gordon H. Fries, John J. Schneider
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<div class="htmlview paragraph">Design, fabrication, and test of large high powered helicopter components in the U.S. Army Heavy Lift Helicopter Advanced Technology Component development program demonstrated the feasibility of efficient, large helicopter components and reduced the risk and cost of future heavy lift helicopter development.
Gordon H. Fries, John J. Schneider
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Blood, 2023
Introduction Hemophagocytic lymphohistiocytosis (HLH) is a pathological condition characterized by excessive inflammation and tissue damage resulting from an aberrant immune system response. HLH can be classified into two distinct categories: primary HLH and secondary HLH. Secondary hemophagocytic lymphohistiocytosis (HLH)
Krunal Trivedi +3 more
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Introduction Hemophagocytic lymphohistiocytosis (HLH) is a pathological condition characterized by excessive inflammation and tissue damage resulting from an aberrant immune system response. HLH can be classified into two distinct categories: primary HLH and secondary HLH. Secondary hemophagocytic lymphohistiocytosis (HLH)
Krunal Trivedi +3 more
openaire +1 more source
Hemophagocytic lymphohistiocytosis (HLH) can be categorized as either primary (familial, generally occurring in infants) or secondary (sHLH, occurring at any age in association with a variety of conditions) and is mainly triggered by infections, autoimmune diseases, and malignant conditions.
Lubna, Ghani +2 more
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Lubna, Ghani +2 more
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2017
Hemophagocytic lymphohistiocytosis (HLH) in adolescent and adult patients (aHLH) is getting increasing attention due to an assumed rising incidence, a better pathophysiologic understanding, and a growing arsenal of therapeutic ammunition. For many years HLH used to be a domain of pediatrics and was almost totally neglected in adults.
Paul La Rosée, Rafal Machowicz
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Hemophagocytic lymphohistiocytosis (HLH) in adolescent and adult patients (aHLH) is getting increasing attention due to an assumed rising incidence, a better pathophysiologic understanding, and a growing arsenal of therapeutic ammunition. For many years HLH used to be a domain of pediatrics and was almost totally neglected in adults.
Paul La Rosée, Rafal Machowicz
openaire +1 more source
Journal of Pediatric Hematology/Oncology, 2013
Hemophagocytic lymphohistiocytosis (HLH) associated with visceral leishmaniasis (VL) is a very rare phenomenon. We report the first known North American case in a 21 month old boy. He was initially diagnosed with Epstein Barr virus (EBV) triggered HLH and treated with the international treatment protocol, HLH-2004.
Gurpreet, Singh +6 more
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Hemophagocytic lymphohistiocytosis (HLH) associated with visceral leishmaniasis (VL) is a very rare phenomenon. We report the first known North American case in a 21 month old boy. He was initially diagnosed with Epstein Barr virus (EBV) triggered HLH and treated with the international treatment protocol, HLH-2004.
Gurpreet, Singh +6 more
openaire +2 more sources