نتایج جستجو برای: hemolytic disease

تعداد نتایج: 1501795  

Journal: :The Journal of the American Board of Family Practice 1991
A C Cutlip K M Gross M J Lewis

The human parvovirus (HPV) is believed to be the causative agent of erythema infectiosum, or fifth disease. 1 Transient aplastic crisis linked to HPV infection has been described in several types of hemolytic anemias, congenital or acquired, such as sickle cell disease, thalassemia, autoimmune hemolytic anemias, and hereditary spherocytosis.2-8 In some instances, the underlying hemolytic anemia...

Journal: :iranian journal of immunology 0
roya payam khaja pasha stemcore laboratories, sprott centre for stem cell research, ottawa health research institute, ottawa, canada fazel shokri department of immunology, school of public health, tehran university of medical sciences

rhd antigen is the most immunogenic and clinically significant antigen of red blood cells after abo system. it has historically been associated with hemolytic disease of the newborn (hdn) which is now routinely prevented by the administration of polyclonal anti-d immunoglobulin. this management of hdn has proven to be one of the most successful cases of prophylactic treatment based on antibody ...

2018
Amer A. Lardhi Abdullah K. Al-Mutairi Mohammed H. Al-Qahtani Atheer K. Al-Mutairi

Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented wi...

Journal: :Haematologica 2013
Mehdi Nouraie Janet S Lee Yingze Zhang Tamir Kanias Xuejun Zhao Zeyu Xiong Timothy B Oriss Qilu Zeng Gregory J Kato J Simon R Gibbs Mariana E Hildesheim Vandana Sachdev Robyn J Barst Roberto F Machado Kathryn L Hassell Jane A Little Dean E Schraufnagel Lakshmanan Krishnamurti Enrico Novelli Reda E Girgis Claudia R Morris Erika Berman Rosenzweig David B Badesch Sophie Lanzkron Oswaldo L Castro Jonathan C Goldsmith Victor R Gordeuk Mark T Gladwin

The intensity of hemolytic anemia has been proposed as an independent risk factor for the development of certain clinical complications of sickle cell disease, such as pulmonary hypertension, hypoxemia and cutaneous leg ulceration. A composite variable derived from several individual markers of hemolysis could facilitate studies of the underlying mechanisms of hemolysis. In this study, we asses...

Journal: :Neurology India 2008
Chitela Sita Ramu Garuda Butchi Raju Kolli Satya Rao Kolichana Venkateswarlu

Neurological complications of hemolytic anemias are rather uncommon. We are reporting two cases of hemolytic anemia presenting as chorea and recurrent ischemic stroke. The first one is a case of chorea in a patient with sickle cell trait. Reviewing the literature we could find only one case report of chorea in sickle cell disease disease. The second is a case of recurrent ischemic stroke in her...

2013
Yun Hwa Jung Sang Bong Han Young Jae Park In Sook Woo Baik Kee Cho Chi Wha Han

REFERENCES 1. Mayer B, Yurek S, Kiesewetter H, Salama A. Mixed-type autoimmune hemolytic anemia: differential diagnosis and a critical review of reported cases. Transfusion 2008;48:2229-34. 2. Sudha Reddy VR, Samayam P, Ravichander B, Bai U. Autoimmune hemolytic anemia: mixed type-a case report. Indian J Hematol Blood Transfus 2011;27:107-10. 3. Hoffman PC. Immune hemolytic anemia-selected topi...

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