Results 71 to 80 of about 22,042 (204)

Complete Recovery of Ischemic Cardiomyopathy from Thrombotic Thrombocytopenic purpura

Clinical Medicine Insights: Cardiology, 2011
A 50 year old male HIV patient on antiretroviral therapy was admitted for chest pain. Upon admission, the patient was found to have elevated cardiac enzymes, acute thrombocytopenia, hemolytic anemia, acute pancreatitis and acute renal failure.
Sainath Gaddam, Lata Pablani, Vinod Chainani, Ravi Raj Kavuda, Tarun Nagrani, Georges Abou Rjaili, Meekoo Dhar, James C Lafferty   +7 more
doaj   +1 more source

Thrombocytopeniak. [PDF]

, 2014
Thrombocytopenia means low platelet count. This is the most frequent cause of bleeding abnormalities. Petechias, purpuras, mucosal bleeding are typical clinical findings.
Domján, Gyula, Gadó, Klára
core   +1 more source

Severe Acral Necrosis Complicating Thrombotic Microangiopathy in Two Toddlers

Case Reports in Pediatrics, 2020
Acral ischemia/necrosis is one of the rarest but most dreadful complications of thrombotic microangiopathy in pediatric patients. It is more reported with thrombotic thrombocytopenic purpura than with hemolytic and uremic syndrome.
H. Nassih, Z. Lazrak, S. Younous
doaj   +1 more source

Редкое клиническое наблюдение тромботической тромбоцитопенической пурпуры у больной 16 лет [PDF]

, 2016
Описание случая диагностики и течения тромботической тромбоцитопенической пурпуры у девочки 16 ...
Бадосова, Т. В., Романова, Т. А., Чернявская, Е. К.   +2 more
core   +1 more source

Pulmonary Tuberculosis Complicated by Thrombotic Thrombocytopenic Purpura: A Case Report and Literature Review

Infection and Drug Resistance
Jun Zheng,1 Xiaohong Pan,2 Yiyun Jiang3 1Department of Rehabilitation, Nanxing Health Service Center, Shangcheng, Hangzhou, Zhejiang, 310000, People’s Republic of China; 2Tuberculosis Care Unit, Hospital of Integrated Traditional Chinese and Western ...
Zheng J, Pan X, Jiang Y
doaj  

Idiopathic combined, autoantibody-mediated ADAMTS-13/factor H deficiency in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome in a 17-year-old woman: a case report

Journal of Medical Case Reports, 2011
Introduction Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome is a life-threatening condition with various etiopathogeneses. Without therapy approximately 90% of all patients die from the disease. Case presentation We report the case of a 17-
Patschan Daniel, Korsten Peter, Behlau Arne, Vasko Radovan, Heeg Malte, Sweiss Nadera, Müller Gerhard A, Koziolek Michael   +7 more
doaj   +1 more source

Available evidence and outcome of off-label use of rituximab in clinical practice [PDF]

, 2013
Purpose: To analyze the therapeutic indications for off-label use of rituximab, the available evidence for its use, the outcomes, and the cost. Methods: This was a retrospective analysis of patients treated with rituximab for off-label indications from ...
A. Agustí, A. Ferrer, A. López, A. Vallano, AS Bomback, B Coiffier, B Terrier, BD Cheson, BH Rovin, C Díaz-Lagares, C Melander, C. Alerany, DM Arnold, EM Allen Van, F Zaja, GJ Weiner, H Schulz, HC Kluin-Nelemans, I. Danés, J Narváez, J. A. Bosch, J. Cortés-Hernández, J. Martínez, JT Merrill, JZ Gillis, L Lightstone, M Pfreundschuh, M Ramos-Casals, M Ramos-Casals, M Trachana, MC Conde García, P Feugier, SJ Butterly, T Hampton, T Robak   +34 more
core   +2 more sources

The effect of single nucleotide polymorphisms and mutations on congenital thrombotic thrombocytopenic purpura phenotype [PDF]

, 2017
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease with a reported incidence of 6 cases per million per year in the UK. It is characterised by episodes of microangiopathic haemolytic anaemia and thrombocytopenia, with the ...
Tate, H., Tate, H.
core  

Thrombotic Thrombocytopenic Purpura [PDF]

Proceedings of the Royal Society of Medicine, 1959
J, LORBER, J L, EMERY
openaire   +2 more sources

Effect of blood groups on acquired and congenital thrombotic thrombocytopenic purpura and clinical correlation: Multi-center Turkish cohort study

Hematology, Transfusion and Cell Therapy
Background: Thrombotic thrombocytopenic purpura (TTP) is a microangiopathic hemolytic anemia associated with ADAMTS-13 deficiency, a cleaving protease of von Willebrand factor (vWF).
Cevat İlteriş Kıkılı, Damla Ortaboz, Melek Yanaşık, Muhlis Cem Ar, Sevgi Kalayoğlu Beşışık   +4 more
doaj   +1 more source