Results 101 to 110 of about 22,112 (212)

Hemophagocytic Lymphohistiocytosis Complicating Myelodysplasia [PDF]

open access: yes, 2014
We describe a 62-year-old patient with a 4-year history of myelodysplasia who later developed striking features that included massive splenomegaly, rapidly evolving visual loss and a sensorimotor polyneuropathy.
Belleyo-Belkasem, Carima   +4 more
core   +2 more sources

Adult cancer-related hemophagocytic lymphohistiocytosis – a challenging diagnosis: a case report

open access: yesJournal of Medical Case Reports, 2017
Background Adult hemophagocytic lymphohistiocytosis is a secondary immunopathologic phenomenon, mainly secondary to malignancy, infection, or autoimmune disorders.
Michael A. Hust   +4 more
doaj   +1 more source

Fulminant systemic capillary leak syndrome due to C1 inhibitor deficiency complicating acute dermatomyositis: a case report [PDF]

open access: yes, 2014
INTRODUCTION: Dermatomyositis is a chronic inflammatory disorder characterized by muscular and dermatologic symptoms with variable internal organ involvement.
Andreas Brunauer   +5 more
core   +1 more source

Clonal origin of Epstein-Barr virus-infected T/NK-cell subpopulations in chronic active Epstein-Barr virus infection [PDF]

open access: yes, 2010
Clonal expansion of Epstein-Barr virus (EBV) infected B-cells occasionally occurs in immunocompromized subjects. EBV-infected T/natural killer (NK)-cells proliferate in patients with chronic active EBV infection (CAEBV) that is a rare mononucleosis ...
Goichi Toshimoto   +10 more
core   +1 more source

A Case of Refractory Langerhans Cell Histiocytosis Complicated with Hemophagocytic Lymphohistiocytosis Rescued by Cord Blood Transplantation with Reduced-intensity Conditioning [PDF]

open access: yes, 2017
 We diagnosed a female infant with Langerhans cell histiocytosis (LCH) who was refractory to conventional chemotherapy. She showed refractory inflammation that was complicated with hemophagocytic lymphohistiocytosis (HLH) during LCH chemotherapy ...
Kanamitsu, Kiichiro   +4 more
core   +1 more source

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis

open access: yesHaematologica, 2010
Background Familial hemophagocytic lymphohistiocytosis is a fatal disease characterized by immune dysregulation from defective function of cytotoxic lymphocytes.
Hoi Soo Yoon   +19 more
doaj   +1 more source

Disseminated Fusarium oxysporum Infection in Hemophagocytic Lymphohistiocytosis [PDF]

open access: yes, 2018
: The portal of entry of disseminated Fusarium spp. infections is still not clearly defined. We report on a disseminated Fusarium oxysporum infection occurring during a long period of severe neutropenia in a child with hemophagocytic lymphohistiocytosis.
Albisetti, M.   +5 more
core  

Haemophagocytic lymphohistiocytosis: An uncommon clinical presentation of tuberculosis [PDF]

open access: yes, 2012
published_or_final_versio
Chan, JFW   +9 more
core  

Síndrome hemofagocítico asociado a tumor primario oculto : reporte de un caso [PDF]

open access: yes, 2016
Se comunica un caso de un hombre joven con carcinoma primario desconocido asociado a un síndrome hemofagocítico para reportar esta asociación, que para nuestro conocimiento, no ha sido publicada hasta la fecha y realizar una revisión de ambas patologías ...
Abaca, María Celeste   +5 more
core  

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