Results 161 to 170 of about 6,796 (202)
Hemophagocytosis Associated With Hepatitis A and E Coinfection in a Young Child
Indian Journal of Hematology and Blood Transfusion, 2011 We report and discuss a unique case of hemophagocytosis associated with hepatitis A and E coinfection in a young child which has never been reported earlier in children.
Ketan Kulkarni +2 more
exaly +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Hemophagocytosis of Sickle Cells
New England Journal of Medicine, 2020Hemophagocytosis of Sickle Cells A 60-year-old man with sickle cell disease presented with fatigue and shortness of breath.
Felix, Mensah, Monica, Pilichowska
openaire +2 more sources
Rickettsial infection with hemophagocytosis
Tropical Doctor, 2010A five-year-old girl admitted with scrub typhus developed multiple organ dysfunction associated with hyperferritinaemia, hypofibrinogenaemia and hyperlipidaemia. Bone marrow aspiration studies confirmed haemophagocytic lymphohistiocytosis (HLH). HLH is a syndrome characterized by the uncontrolled activation and proliferation of macrophages and T-cells
M P, Jayakrishnan, John, Veny, M, Feroze
openaire +2 more sources
Value of Hemophagocytosis in the Diagnosis of Hemophagocytic Lymphohistiocytosis in Critically Ill Patients [PDF]
European Journal of HaematologyBackground: Ferritin is an established biomarker in the diagnosis of secondary hemophagocytic lymphohistiocytosis (HLH), which is diagnosed by the HLH-2004 criteria.
Jana Ihlow +2 more
exaly +2 more sources
Sensorimotor neuropathy in hemophagocytosis syndrome
Acta Neurologica Scandinavica, 1991Hemophagocytosis syndromes are uncommon disorders marked by generalized proliferation of benign histiocytes and multiple organ failure. A 24-year-old woman presented with a fulminant illness consisting of fever, hepatic insufficiency and anemia, followed by respiratory compromise, cardiomyopathy, and uremia. She developed a sensorimotor polyneuropathy,
L S, Honig +3 more
openaire +2 more sources
HEMOPHAGOCYTOSIS COMPLICATING KAWASAKI DISEASE
Pediatric Hematology and Oncology, 2000A 6-year-old boy developed hemophagocytic syndrome during the recurrent course of Kawasaki disease. Despite the appropriate treatment modalities for Kawasaki disease, he developed pancytopenia, marked hepatosplenomegaly, high-grade fever, hyperferritinemia, hypertriglyceremia, and evidence of hemophagocytosis in the liver biopsy.
W, al-Eid +3 more
openaire +2 more sources
Hemophagocytosis and Acute Monoblastic Leukemia
Pediatric Hematology and Oncology, 1989A 16-month-old girl presented with hepatosplenomegaly and pancytopenia. Bone marrow aspiration showed a florid increase in macrophages with marked hemophagocytosis. She subsequently improved spontaneously with no therapeutic intervention, but 2 months later presented with frank acute monoblastic leukemia.
L, Russell, N J, Shaw, O B, Eden
openaire +2 more sources
Pancytopenia resulting from hemophagocytosis in malaria
The Pediatric Infectious Disease Journal, 2002Pancytopenia in an acutely ill child is commonly a result of bone marrow suppression. Rarely pancytopenia is a manifestation of inappropriate macrophage activation associated with hemophagocytosis. Viral infections account for most cases of secondary hemophagocytosis.
Alex, Zvulunov +2 more
openaire +2 more sources
Interstitial hemophagocytosis in hemophagocytic lymphohistiocytosis
Kidney International, 2023Miroslav, Sekulic +3 more
openaire +2 more sources