نتایج جستجو برای: hemophagocytic

تعداد نتایج: 3846  

MOJTABA TABARESTANI,

Hemophagocytic syndrome is a non-malignant process that is characterized clinically by fever, hepatomegaly, splenomegaly, pancytopenia in peripheral blood, and reactive histiocytes in the bone marrow. Bacterial infectious diseases like typhoid fever and brucellosis and viral infections including CMV, herpes viruses, and Epstein-Barr virus are diagnosed as the cause of this syndrome. In thi...

Journal: :archives of pediatric infectious diseases 0
roxana m. ghanaie 1 pediatric infections research center, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) reza shiari department of pediatrics, division of pediatric rheumatology, mofid children hospital, shahid beheshti university of medical sciences, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) abdollah karimi 1 pediatric infections research center, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) shahnaz armin 1 pediatric infections research center, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) alireza fahimzad 1 pediatric infections research center, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) faride shiva 1 pediatric infections research center, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

hemophagocytic lymphohistiocytosis (hlh) is an aggressive and potentially life-threatening disease and has to be considered in the differential diagnosis of many conditions. hlh comprises two different conditions that are difficult to differentiate; familial hemophagocytic lymphohistiocytosis (fhlh) or familial erythrophagocytic lymphohistiocytosis (fel), and secondary hemophagocytic syndromes ...

Journal: :The AIDS reader 2007
Liron Pantanowitz Bruce J Dezube

Sanchez and colleagues1 report a case of histoplasmosis-associated reactive hemophagocytic syndrome in a 61-year-old HIV-infected man. The association of hemophagocytic syndrome with HIV infection is important for several reasons: (1) Many of the features of the hemophagocytic syndrome are not specific in this setting, and, hence, may be easily overlooked or misdiagnosed. (2) The hemophagocytic...

Journal: :medical journal of islamic republic of iran 0
mojtaba tabarestani from tile department of clinical pathology, imam reza hospital, mashhad university of medical sciences, mashhad, islamic republic of iran.

hemophagocytic syndrome is a non-malignant process that is characterized clinically by fever, hepatomegaly, splenomegaly, pancytopenia in peripheral blood, and reactive histiocytes in the bone marrow. bacterial infectious diseases like typhoid fever and brucellosis and viral infections including cmv, herpes viruses, and epstein-barr virus are diagnosed as the cause of this syndrome. in this pap...

2017
Zakaria Hindi Abdallah A Khaled Ashraf Abushahin

Introduction Hemophagocytic syndrome or hemophagocytic lymphohistiocytosis is a rare condition characterized by excessive inflammation that is thought to be caused by the absence of normal downregulation of activated macrophages and lymphocytes. The treatment of hemophagocytic lymphohistiocytosis can depend on whether it is primary or secondary. In secondary hemophagocytic lymphohistiocytosis, ...

Journal: :Haematologica 2015
Sebastian Fn Bode Sandra Ammann Waleed Al-Herz Mihaela Bataneant Christopher C Dvorak Stephan Gehring Andrew Gennery Kimberly C Gilmour Luis I Gonzalez-Granado Ute Groß-Wieltsch Marianne Ifversen Jenny Lingman-Framme Susanne Matthes-Martin Rolf Mesters Isabelle Meyts Joris M van Montfrans Jana Pachlopnik Schmid Sung-Yun Pai Pere Soler-Palacin Uta Schuermann Volker Schuster Markus G Seidel Carsten Speckmann Polina Stepensky Karl-Walter Sykora Bianca Tesi Thomas Vraetz Catherine Waruiru Yenan T Bryceson Despina Moshous Kai Lehmberg Michael B Jordan Stephan Ehl

Hemophagocytic lymphohistiocytosis is a hyperinflammatory syndrome defined by clinical and laboratory criteria. Current criteria were created to identify patients with familial hemophagocytic lmyphohistiocytosis in immediate need of immunosuppressive therapy. However, these criteria also identify patients with infection-associated hemophagocytic inflammatory states lacking genetic defects typic...

برجیان, دکتر لیلا, نظمیه, حسین,

Expression of Hemophagocytic Lymphohistiocytosis with Hepatic Dysfunction in a 50 days Old Infant L. Borjian MD , H. Nazmieh MSc Received: 27/03/07 Sent for Revision: 13/06/07 Received Revised Manuscript: 08/07/07 Accepted: 26/07/07 Background and Objective: The Hemophagocytic Lymphohistiocytosis (HLH) is a rare disease with the pathologic hallmark of having aggressive proliferation o...

Journal: :Arthritis & rheumatology 2014
Laurence Fardet Lionel Galicier Olivier Lambotte Christophe Marzac Cedric Aumont Doumit Chahwan Paul Coppo Gilles Hejblum

OBJECTIVE Because it has no unique clinical, biologic, or histologic features, reactive hemophagocytic syndrome may be difficult to distinguish from other diseases such as severe sepsis or hematologic malignancies. This study was undertaken to develop and validate a diagnostic score for reactive hemophagocytic syndrome. METHODS A multicenter retrospective cohort of 312 patients who were judge...

2016
El Mehdi Mahtat Maryem Zine Mohamed Allaoui Malika Kerbout Nezha Messaoudi Kamal Doghmi Mohamed Mikdame

BACKGROUND Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. CASE PRESENTATION We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated wit...

2016
Satoru Teshigawara Yoshinori Katada Yuichi Maeda Maiko Yoshimura Eriko Kudo-Tanaka Soichiro Tsuji Yoshinori Harada Masato Matsushita Shiro Ohshima Kotaro Watanabe Takahiro Kumode Yoshihiko Hoshida Yukihiko Saeki

BACKGROUND Hemophagocytic lymphohistiocytosis associated with autoimmune diseases is seen in patients with systemic juvenile idiopathic arthritis, adult-onset Still's disease, and systemic lupus erythematosus, whereas it is rarely seen in patients with dermatomyositis. In addition, central nervous system involvement with dermatomyositis is rare. To the best of our knowledge, this is the first c...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید