نتایج جستجو برای: autoimmune thrombocytopenia

تعداد نتایج: 84689  

Journal: :Blood 1998
N Ajzenberg M Dreyfus C Kaplan J Yvart B Weill G Tchernia

Thrombocytopenia detected during pregnancy addresses the issue of its mechanism and of the possible occurrence of neonatal thrombocytopenia. To further investigate these issues, 50 women referred to us because of thrombocytopenia detected during pregnancy (platelet count, <150 x 10(9)/L), were extensively studied, as well as their offspring. Among these thrombocytopenic women, we used the thres...

Journal: :International journal of medical science and clinical research studies 2022

Splenectomy can treat conditions characterized by hemolysis or thrombocytopenia caused autoantibodies splenic reticuloendothelial function, as well disorders massive splenomegaly and hypersplenism with cytopenias, such hereditary spherocytosis, transfusion-dependent thalassemia, immune thrombocytopenia, autoimmune hemolytic anemia, marginal zone lymph is no longer used for Hodgkin disease stagi...

Journal: :Annals of the rheumatic diseases 1990
E M Hay M Makris J Winfield D A Winfield

Autoimmune haematological complications in dermatomyositis are very uncommon. This case report describes autoimmune haemolytic anaemia and thrombocytopenia in a patient with dermatomyositis and pulmonary fibrosis.

2017
Juárez Salcedo Luis Miguel Gil-Fernández Juan José

Autoimmune cytopenias (AICs) are frequently associated with chronic lymphocytic leukemia (CLL). The most common of these AICs is autoimmune hemolytic anemia (AIHA); the second most is immune thrombocytopenia (ITP). Here, we report on a patient with CLL-associated ITP, with thrombocytopenia refractory to corticosteroids and intravenous immunoglobulins, in which continuous oral treatment with Elt...

2010
Henedina Antunes Ruben Rocha Nicole Silva Teresa Pontes Ana Antunes Sofia Martins

We report a case of a 15-year-old boy with autoimmune hepatitis lacking common serologic markers and normal gammaglobulinemia associated with immune thrombocytopenia and family history of psoriasis. He presented to our department with a 4-year history of a cervical posterior lymphadenopathy and recent petechiae. Previous laboratory results 6 months before already showed hepatocellular injury. A...

Journal: :Haematologica 2016
Lamiae Grimaldi-Bensouda Clémentine Nordon Marc Michel Jean-François Viallard Daniel Adoue Nadine Magy-Bertrand Jean-Marc Durand Philippe Quittet Olivier Fain Bernard Bonnotte Anne-Sophie Morin Nathalie Morel Nathalie Costedoat-Chalumeau Brigitte Pan-Petesch Mehdi Khellaf Antoinette Perlat Karim Sacre François Lefrere Lucien Abenhaim Bertrand Godeau

This prospective observational cohort study aimed to explore the clinical features of incident immune thrombocytopenia in adults and predictors of outcome, while determining if a family history of autoimmune disorder is a risk factor for immune thrombocytopenia. All adults, 18 years of age or older, recently diagnosed with immune thrombocytopenia were consecutively recruited across 21 hospital ...

2008
Chih-Hsiung Yang Chia-Yu Chu Sung-Jan Lin

The pathogenesis of vitiligo has been proposed as a destruction of melanocytes by autoimmune processes. Evans syndrome is the combination of autoimmune hemolytic anemia and immune-mediated thrombocytopenia. The antiphospholipid syndrome is characterized by arterial/venous thrombosis, recurrent pregnancy loss, or thrombocytopenia in the presence of antiphospholipid antibodies. We present a case ...

Journal: :Transfusion medicine 2006
N Ahrens C Pagenkopf H Kiesewetter A Salama

CD47 deficiency results in lethal autoimmune haemolytic anaemia (AIHA) and mild spontaneous thrombocytopenia in non-obese diabetic mice. It is unknown whether CD47 has an impact on AIHA of the warm type or autoimmune thrombocytopenia (ITP) in humans. Healthy blood donors (n= 11), patients with AIHA (n= 13), patients with ITP (n= 18) and one patient with Rh(null) phenotype were investigated. CD4...

2011
Hye Jin Oh Myung Jae Yun Seong Tae Lee Seung June Lee So Yeon Oh In Sohn

We report a case of a 51-year-old woman with Evans syndrome (autoimmune hemolytic anemia and primary immune thrombocytopenia) and hypothyroidism. She was previously diagnosed with Hashimoto's thyroiditis in 1994 (age, 35) and autoimmune hemolytic anemia (AIHA) 3 years ago. She was treated with oral prednisolone. After a period, in which the anemia waxed and waned, there was an abrupt developmen...

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