نتایج جستجو برای: macrophage activating syndrome hemophagocytic lymphohistiosytosis

تعداد نتایج: 728386  

Journal: :Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2015
Corina Silvia Pop Gabriel Becheanu Dorina Calagiu Petruţa-Violeta Jantea Dragoş Mihai Rădulescu George Pariza Carmen-Iuliana Mavrodin Adriana Bold Adrian Costache Roxana Maria Nemeş

We report a case of CMV (cytomegalovirus) infection in a Crohn's disease patient, resulting in severe hemophagocytic syndrome and death. A 63-year-old man with a 10-year history of ileal and colonic Crohn's disease presented with general malaise, loss of appetite and weight loss over the last month. He was in clinical remission for two years, with maintenance therapy 5-Aminosalicylic acid (5-AS...

Journal: :American Journal of Hematology 2011

Journal: :Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 2015
Wan Fariza Wan Jamaludin Petrick Periyasamy Wan Rahiza Wan Mat S Fadilah Abdul Wahid

Infection associated hemophagocytic syndrome is increasingly recognized as a potentially fatal complication of dengue fever. It should be suspected with prolonged fever beyond seven days associated with hepatosplenomegaly, hyperferritinemia, worsening cytopenias and development of multiorgan dysfunction. Surge of similar pro-inflammatory cytokines observed in dengue associated hemophagocytic sy...

Journal: :Blood 2013
Xi Wen Zhao Roel P Gazendam Agata Drewniak Michel van Houdt Anton T J Tool John L van Hamme Iwan Kustiawan Alexander B Meijer Hans Janssen David G Russell Lisette van de Corput Kiki Tesselaar Jaap J Boelens Ingrid Kuhnle Jutte Van Der Werff Ten Bosch Taco W Kuijpers Timo K van den Berg

Familial hemophagocytic lymphohistiocytosis (FHL) is caused by genetic defects in cytotoxic granule components or their fusion machinery, leading to impaired natural killer cell and/or T lymphocyte degranulation and/or cytotoxicity. This may accumulate into a life-threatening condition known as macrophage activation syndrome. STXBP2, also known as MUNC18-2, has recently been identified as the d...

Journal: :Blood 2003
Mark D Fleming Jack L Pinkus Marcia V Fournier Sarah W Alexander Carmen Tam Massimo Loda Stephen E Sallan Kim E Nichols David F Carpentieri Geraldine S Pinkus Barrett J Rollins

It has been suggested that a switch in chemokine receptor expression underlies Langerhans cell migration from skin to lymphoid tissue. Activated cells are thought to down-regulate CCR6, whose ligand macrophage inflammatory protein-3 alpha (MIP-3 alpha)/CCL20 is expressed in skin, and up-regulate CCR7, whose ligands are in lymphoid tissues. In Langerhans cell histiocytosis (LCH), pathologic Lang...

Journal: :Reumatologia clinica 2017
Leslye F Conde Karla P Aedo Tatiana Miraval-Niño de Guzmán

Reactive hemophagocytic lymphohistiocytosis (HLH), or macrophage activation syndrome (MAS), is an unusual complication of systemic inflammatory diseases.1 Its association with juvenile idiopathic arthritis (JIA) is rare and treatment must be immediate. We report the case of a girl in whom we detected this association and treated it successfully with a drug that is not first-line therapy because...

Journal: :The Medical journal of Malaysia 2004
G G Gan G I Eow A Teh S C Ng J V Sangkar

Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs. It is usually difficult to distinguish from other hemophagocytic syndrome in the absence of family history. It rarely manifests in adults. Chemotherapy is usually indicated. Here,...

Journal: :Journal of Korean Medical Science 2003
Young Mi Kim Yoon Jin Lee Sang Ook Nam Su Eun Park Ji Yoen Kim Eun Yup Lee

A 13-yr-old female was admitted to our hospital with fever, seizure, and cervical lymphadenopathy. Laboratory data showed pancytopenia, elevation of serum transaminase, lactate dehydrogenase, triglyceride, and ferritin levels. Lymph node biopsy revealed features of Kikuchi's disease and there were signs of histiocytosis and hemophagocytic phenomenon in bone marrow. She recovered after treatment...

Journal: :Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2006
Teruchika Yamada Yuichi Handa Teppei Kamikawa Hiroyuki Machino Kenji Suzuki Kazunori Miyata

THE CASE A 44-year-old female. Developed polyarthralgia in August 2002. The patient was diagnosed with systemic lupus erythematosus (SLE) in November, due to polyarthralgia, leukopenia, anti ds-DNA antibody positive, antinuclear antibody positive, and false positive serologic test for syphilis. Hypocomplementemia continued even after the steroid treatment was conducted with insufficient control...

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