نتایج جستجو برای: hemophagocytic syndrome

تعداد نتایج: 624474  

2014
Babak Tamizifar Golnaz Samadi Maryam Rismankarzadeh

Hemophagocytic syndrome (HPS) is an uncommon manifestation in systemic lupus erythematosus (SLE). Clinical features of HPS include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. HPS comprises primary and reactive forms. Herein, we describe a case of untreated SLE with HPS as one of the first manifestations of systemic Lupus.

Journal: :Acta dermatovenerologica Croatica : ADC 2004
Joanna Maj Tomasz Kolodziej Zdzislaw Wozniak

A case of a 62-year-old woman with recurrent subcutaneous nodules, fever and pancytopenia diagnosed as subcutaneous T-cell lymphoma is presented. Incision biopsy revealed lobular panniculitis with an inflammatory infiltrate of atypical T lymphocytes. She was treated with 7 courses of CHOP with transient remission, and she died after 17 months of disease from fatal hemorrhagic complications due ...

2015
Ashish Rajput Isabelle Bence-Bruckler Lothar Huebsch Peter Jessamine Baldwin Toye Ruth Padmore

Hemophagocytic lymphohistiocytosis (HLH) is a potentially life-threatening clinical syndrome caused by uncontrolled activation of lymphocytes and histiocytes resulting in high levels of cytokines. Acquired HLH occurs in autoimmune, inflammatory, infectious, and immunosuppressive disorders. Prompt identification and treatment of an underlying triggering cause improves clinical outcome.

2013
Pantelis Antonodimitrakis Cecilia Wassberg Spyridon Gerovasileiou Johan Back Roger Hällgren Björn Olsen

Hemophagocytic lymphohistiocytosis (HLH) is an aggressive inflammatory syndrome that results from inappropriate activation of the immune system. HLH has a high mortality if not treated. We describe a case of a fulminant HLH, associated with a reactivation of an EBV infection. The patient responded well to steroid treatment.

Journal: : 2021

In most cases, COVID-19 has a favorable outcome. However, the risk of developing critical forms disease, including secondary hemophagocytic lymphohistiocytosis HLH (cytokine storm syndrome), remains high. This dictates interest in studying pathogenetic mechanisms, features clinical picture, laboratory and instrumental criteria for covid-19 disease. The article analyzes causes acute respiratory ...

2014
Metin Kanıtez Mahir Kapmaz Nilufer Alpay Fatih Selcukbiricik Atahan Çağatay Reyhan Diz-Küçükkaya

Highly active antiretroviral therapy (HAART) has markedly decreased human immunodeficiency virus- (HIV-) related mortality and the incidence of opportunistic infections. The dramatic reduction in HIV-1 RNA and increase in CD4 lymphocyte count mean a recovery in immune function. This restoration in immune function may be associated with paradoxical deterioration in subclinical opportunistic infe...

Journal: :Japanese Journal of Clinical Immunology 2009

Journal: :Journal of Infection and Chemotherapy 2012

2013
Soheila Khalilzadeh Maryam Hassanzad Elaheh Heydarian Fard Atosa Dorudinia Ali Akabr Velayati

Visceral Leishmaniasis (VL), a systemic infection of the reticuloendotherlial system, is caused by a parasitic infection. The co-occurrence of VL and hemophagocytic syndrome (HPS) has been previously reported in several studies. In this report we present two cases of HPS and VL among members of the same family.

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