نتایج جستجو برای: immune thrombocytopenic purpura

تعداد نتایج: 272547  

2014
Hanjun Kim Sang Sun Hwang Young Uh Juwon Kim Kap Jun Yoon Ji-Yong Lee

A 46-year-old female presented to the emergency room due to the chief complaint of left-sided weakness. By imaging study, she was diagnosed with cerebral infarction. Thrombolytic and antiplatelet agents were not considered due to the "golden hour" for treatment having passed and a low platelet count. The peripheral blood smear, bone marrow biopsy, and aspirate findings were consistent with immu...

Esfahani H, Eshghi P, Madani F, Malek F,

Treatment of severe Immune Thrombocytopenic purpura (ITP) accompanied by life-threatening bleeding events is challenging and a combination of treatment measures should be undertaken to rapidly increase the platelet count. Herein, we report a case of severe ITP in a seven-year-old boy who suffered from massive bleeding which was totally unresponsive to conventional therapeutic interventions. Sin...

2004

Individual reprints of this article are not available. Address correspondence to Roberto Stasi, MD, Department of Medical Sciences, “Regina Apostolorum” Hospital, Via S. Francesco, 50, 00041 Albano Laziale, Italy (e-mail: [email protected]). ITP = immune thrombocytopenic purpura; IVIg = intravenous immunoglobulin Primary immune thrombocytopenic purpura (ITP), also referred to as idiopathi...

Journal: :Le infezioni in medicina : rivista periodica di eziologia, epidemiologia, diagnostica, clinica e terapia delle patologie infettive 2013
Mehmet Sinan Dal Tuba Dal Recep Tekin Erdal Bodakçi Yakup Düzköprü Mehmet Orhan Ayyildiz

Tuberculosis is still one of the most prevalent and fatal infectious diseases in spite of considerable improvements in medical science. Splenic tuberculosis is a rare form of extrapulmonary tuberculosis. There are limited numbers of cases in which immune thrombocytopenia is associated with splenic tuberculosis. We report a case of immune thrombocytopenic purpura due to splenic tuberculosis. Our...

Journal: :Blood 1984
G M Shaw J Axelson J G Maglott A F LoBuglio

In this report we describe the use of an 125I-Staphylococcal protein A (SPA) assay to measure platelet-bound IgG in the evaluation of 62 thrombocytopenic patients. Platelets from 150 normal subjects were found to bind 146 +/- 112 molecules of SPA per platelet (mean +/- 2 SD). Nineteen of 20 patients with untreated immune thrombocytopenia had platelet IgG values above this range, with 15 of 20 h...

2016
N. D. B. Ehelepola M. B. K. Gunawardhana T. N. Sudusinghe S. K. D. Sooriyaarachchi S. P. Manchanayake K. L. R. Kalupahana

BACKGROUND Dengue is the most prevalent and fast spreading arboviral infection affecting people. No specific drug is available to treat dengue. Thrombocytopenia with potential of serious hemorrhages is one of the hall mark features of dengue. Immune thrombocytopenic purpura is an autoimmune disease causing thrombocytopenia. If a patient with that gets dengue, we expect severe thrombocytopenia w...

Journal: :Indian Journal of Pharmaceutical Sciences 2022

A systematic review of the efficacy and safety Jianpi Yiqi combined with glucocorticoids in treatment immune thrombocytopenic purpura. Randomized controlled trial therapy glucocorticoid for purpura was retrieved without any restrictions on blindness language. that met inclusion criteria were screened, Revman5.3 software used meta-analysis. total 27 articles included 1716 cases. The results meta...

Journal: :Journal of clinical pathology 1976
D J Jeffries A H Johnson J F Mowbray

Two cases of rubella are described which caused initial problems in laboratory diagnosis due to abnormal features in the immune response. One patient presented with thrombocytopenic purpura and associated circulating immune complexes. The other patient, who was in early pregnancy, had an unusually prolonged rash and a delayed humoral immune response. The possible reasons for the difficulties in...

2010
Sebastián Ben Fabián Rodríguez Carlos Severo Natalia Debat

We will describe the clinical case of a pregnant patient with chronic Immune Thrombocytopenic Purpura who develops preeclampsia syndrome with HELLP syndrome. These concomitant and independent conditions become complex, resulting in thrombocytopenia which creates diagnostic, prognostic and therapeutic inconveniences.

Journal: :Turkish journal of haematology : official journal of Turkish Society of Haematology 2011
Ümmügül Üyetürk Şerife Hülya Arslan Meltem Kurt Yüksel Fevzi Altuntaş

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