نتایج جستجو برای: hemophagocytic

تعداد نتایج: 3846  

Journal: :Blood 2011
Yuuki Murata Takahiro Yasumi Ryutaro Shirakawa Kazushi Izawa Hidemasa Sakai Junya Abe Naoko Tanaka Tomoki Kawai Koichi Oshima Megumu Saito Ryuta Nishikomori Osamu Ohara Eiichi Ishii Tatsutoshi Nakahata Hisanori Horiuchi Toshio Heike

Familial hemophagocytic lymphohistiocytosis (FHL) is a potentially lethal genetic disorder of immune dysregulation that requires prompt and accurate diagnosis to initiate life-saving immunosuppressive therapy and to prepare for hematopoietic stem cell transplantation. In the present study, 85 patients with hemophagocytic lymphohistiocytosis were screened for FHL3 by Western blotting using plate...

2013
Yuji Koike Nao Aoki

Mycoplasma pneumoniae (Mp) sometimes causes immunological complications in children. We present a rare case of hemophagocytic syndrome (HPS) caused by Mp in a previously healthy 7-year-old Japanese girl. A chest radiograph obtained to evaluate the source of her fever showed infiltration in the lower right lung with mild splenomegaly. We could diagnose the patient with HPS on the basis of the he...

Journal: :Blood 2004
Nitin J Karandikar Steven H Kroft Subramanian Yegappan Beverly B Rogers Victor M Aquino Kyung-Mi Lee Vinay Kumar F Javier Guenaga Elaine S Jaffe Daniel C Douek Robert W McKenna

Familial hemophagocytic lymphohistiocytosis (FHL) is an inherited, fatal disorder of infancy. We report here a 17-day-old female infant who presented with high fever, hepatosplenomegaly, hypertriglyceridemia, hypofibrinogenemia, thrombocytopenia, and liver failure. Leukocytosis was detected with circulating "atypical" lymphoid cells. Flow cytometric studies revealed expanded subpopulations of C...

Journal: :Modern rheumatology 1994
R Onishi S Namiuchi

A 63-year-old female, who had been diagnosed with rheumatoid arthritis (RA) 3 years previously, was admitted due to progressive pancytopenia, lymphadenopathy, fever, and weight loss. The physical and laboratory findings fulfilled all of the American Rheumatism Association (ARA) revised criteria for RA. Her bone marrow aspirate revealed a decreased nuclear cell count (1.8 x 10(4) microliters) an...

2015
Jiehao Zhou Dehua Wang Mehdi Nassiri

EBV associated hemophagocytic lymphohistiocytosis and EBV-positive T cell lymphoproliferative disease of childhood share many histologic and clinical features, which sometimes makes it very difficult to render a definitive diagnosis. In this report, we present a 16-year-old male who developed symptoms clinically consistent with EBV associated hematophagocytic lymphohistiocytosis including fulfi...

Journal: :European Journal of Case Reports in Internal Medicine 2014

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