نتایج جستجو برای: hemophagocytic lymphohistocytosis

تعداد نتایج: 3849  

Journal: :The journal of the Japanese Society of Lymphoreticular Tissue research 1997

Journal: :The American Journal of Tropical Medicine and Hygiene 2018

Journal: :Journal of Blood Disorders & Transfusion 2016

Journal: :Blood 2012
Omar S Aljitawi Jamie M Boone

A 34-year-old male with a history of T cell–rich B-cell lymphoma relapsed 1 year after high-dose therapy with recurrent fevers, abdominal pain, and jaundice. He was cachetic with hepatosplenomegaly and ascites. Laboratory findings showed a white blood cell count of 2.7 109/L, hemoglobin 8.7 g/dL, platelets of 21 109/L, hyperbilirubinemia, and no evidence of hemolysis including a negative Coombs...

Journal: :Journal of vector borne diseases 2013
Gajanand Singh Tanwar Anil Lahoti Priya Tanwar Renu Agrawal Punam Chand Khatri Dhanpat Kumar Kochar

order of the mononuclear phagocytic system, characterized by benign, generalized histiocytic proliferation, with marked hemophagocytosis in bone marrow1. Generally, HPS has been related with hematologic diseases, autoimmune diseases, or with various infections1. There are plenty of reports on hemophagocytic syndrome associated with Plasmodium falciparum monoinfetion2–9, but reports on the assoc...

2015
Nicole Beffermann Javier Pilcante Mauricio Sarmiento

INTRODUCTION We present the case of a patient with acquired hemophagocytic syndrome secondary to parainfluenza virus infection, a complication that has not, to the best of our knowledge, been previously reported. CASE PRESENTATION A 33-year-old Chilean man with fever secondary to parainfluenza 2 virus infection developed progressive cholestasis, hepatosplenomegaly, cytopenia and an increased ...

2016
Ramona Vesna Untanu Syed Akbar Stephen Graziano Neerja Vajpayee

Hemophagocytic lymphohistiocytosis (HLH) is an aggressive and life-threating immune dysregulation syndrome characterized by persistent activation of the mononuclear phagocytic system leading to uncontrolled systemic hyperinflammatory response. The proliferation and activation of histiocytes and lymphocytes lead to production of large amounts of cytokines, also called cytokine storm. Hematopoiet...

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...

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