نتایج جستجو برای: thrombocytopenic purpura

تعداد نتایج: 13583  

Journal: :The Journal of the Association of Physicians of India 2012
A K Khobragade A R Chogle R P Ram Joanne Mascarenhas Sweta Kothari Sneha Kawadkar S S Deshpande Dipti Nair Jhoomar Makhija

Thrombotic thrombocytopenic purpura (TTP) is a multisystem disorder characterized by a pentad consisting of thrombocytopenic, microangiopathic hemolytic anemia, renal dysfunction, neurological signs and fever. Coexistence of thrombotic thrombocytopenic purpura and Adult Onset Still's Disease (AOSD) is extremely rare. We report a case of 18 year old girl with AOSD who developed TTP. Neuroimaging...

2017
Marie Scully Christopher Hibbard Bruce Ewenstein

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2001
R H Kok M J Wolfhagen G Klosters

This is the first report of a patient with a syndrome resembling thrombotic thrombocytopenic purpura associated with a recent human parvovirus B19 infection.

Journal: :Journal of nuclear medicine technology 2000
J K MacDonald R A Wilke W E Jacobs

This case report presents a highly unusual finding of ectopic splenic tissue in both the thoracic and abdominal cavities in a patient with recurrent idiopathic thrombocytopenic purpura (ITP).

Journal: :Acta haematologica 1973
S Weitzman A Dvilansky I Yanai

A man with apparently quiescent Hodgkin's disease presented with acute severe isolated thrombocytopenic purpura. Splenectomy revealed macroscopic involvement with Hodgkin's tissue and cured the thrombocytopenia.

Journal: :Blood 1982
J G Kelton P J Powers C J Carter

The measurement of platelet-associated IgG (PAIgG) is a potentially useful diagnostic test for idiopathic thrombocytopenia purpura (ITP). However, the restricted application of PAIgG measurements to thrombocytopenic populations primarily comprised of ITP patients will artificially enhance its diagnosis specificity. For this reason, we performed a prospective study in which the results of a sens...

Journal: :Paediatrica Indonesiana 2023

Henoch-Schonlein Purpura (HSP) is an acute immunoglobulin A (IgA)–mediated disorder characterized by generalized vasculitis. HSP commonly occurs in children. The annual worldwide incidence 13-20 per 100,000 children under 17 years of age.1–3 It non-thrombocytopenic palpable purpura mostly located on the dependent parts like lower extremities and buttocks, arthralgia/arthritis, bowel angina, hem...

2003
Hajime Mizutani Robert W. Engelman

Male (NZW X BXSB)F1 (W/BF,) mice develop systemic autoimmunity involving autoantibodies, progressive thrombocytopenia, lupus nephritis, and degenerative coronary vascular disease with myocardial infarction. Plateletassociated IgG (PAIgG) on the platelet surface mediates platelet destruction by the reticuloendothelial system in the autoimmune thrombocytopenic purpura (ATP) of W/ BF1 mice. Becaus...

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