نتایج جستجو برای: immune mediated hemolytic anemia

تعداد نتایج: 696834  

Journal: :Indian pediatrics 2017
Ritambhra Nada Joseph L Matthews Sagar Bhattad Anju Gupta Surjit Singh

A 10-year-old child presented with prolonged fever, lymphadenopathy, weight loss, oral ulcers, alopecia and parotitis. She later developed arterial thrombosis, poly-serositis, nephritis, myocarditis, sacro-ilitis, autoimmune hemolytic anemia and refractory thrombocytopenia. Though anti-dsDNA was negative, she was diagnosed to have systemic lupus erythematosus (SLE). Terminally, she had pulmonar...

Journal: :Autoimmunity reviews 2013
Kam Newman Mohammad Bagher Owlia Ihab El-Hemaidi Mojtaba Akhtari

There are various immune cytopenias associated with systemic lupus erythematosus (SLE). The most common one is anemia; however, there are different etiologies for the anemia caused by SLE. Anemia could be due to chronic disease, secondary to renal insufficiency, blood loss, drug induced or autoimmune hemolysis. There are other very rare causes of anemia secondary to SLE which include red cell a...

Journal: :Medycyna Weterynaryjna 2021

The aim of this case report is to point out the neurological signs, long term management and MRI lesions suggestive cerebral haemorrhage in a dog with IMHA concurrent thrombocytopenia. A 3.5-year-old intact female Cocker Spaniel was examined for anorexia, weakness, exercise intolerance two collapse episodes. Based on diagnostic procedures primary immune mediated hemolytic anaemia severe thrombo...

Journal: :Journal of cardiovascular ultrasound 2016
Young Joo Park Sang Pil Kim Ho-Jin Shin Jung Hyun Choi

Microangiopathic hemolytic anemia occurs in a diverse group of disorders, including thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, and prosthetic cardiac valves. Hemolytic anemia also occurs as a rare complication after mitral valve repair. In this report, we describe a case of microangiopathic hemolytic anemia following myxoma excision and mitral valve repair, which was presen...

2015
Marielle Igala Daniela Nsame Jennie Dorothée Guelongo Okouango Ova Siham Cherkaoui Bouchra Oukkach Asmae Quessar

Sickle cell anemia results from a single amino acid substitution in the gene encoding the β-globin subunit. Polymerization of deoxygenated sickle hemoglobin leads to decreased deformability of red blood cells. Hashimoto's thyroiditis is a common thyroid disease now recognized as an auto-immune thyroid disorder, it is usually thought to be haemolytic autoimmune anemia. We report the case of a 32...

Journal: :Blood 2010
David Gómez-Almaguer Manuel Solano-Genesta Luz Tarín-Arzaga José Luis Herrera-Garza Olga Graciela Cantú-Rodríguez César Homero Gutiérrez-Aguirre José Carlos Jaime-Pérez

Treatment of autoimmune cytopenias remains unsatisfactory for patients refractory to first-line management. We evaluated the safety and efficacy of low-dose rituximab plus alemtuzumab in patients with steroid-refractory autoimmune hemolytic anemia and immune thrombocytopenic purpura. Nineteen of 21 included patients were assessable for response (11 with immune thrombocytopenic purpura, 8 with a...

Journal: :Haematologica 2011
Nathalie Aladjidi Guy Leverger Thierry Leblanc Marie Quitterie Picat Gérard Michel Yves Bertrand Brigitte Bader-Meunier Alain Robert Brigitte Nelken Virginie Gandemer Hélène Savel Jean Louis Stephan Fanny Fouyssac Julien Jeanpetit Caroline Thomas Pierre Rohrlich André Baruchel Alain Fischer Geneviève Chêne Y Perel

BACKGROUND Autoimmune hemolytic anemia is a rare condition in children. Little is known about its initial presentation and the subsequent progression of the disease. DESIGN AND METHODS Since 2004, a national observational study has been aiming to thoroughly describe cases and identify prognostic factors. Patients from all French hematologic pediatric units have been included if they had a hem...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید