Results 21 to 30 of about 38,572 (225)

Purpura with regular shape in an adolescent: Beware of dermatitis artefacta

Frontiers in Pediatrics, 2022
BackgroundPurpura is common in pediatric patients, mostly diagnosed as IgA-related vasculitis (Henoch–Schönlein purpura), idiopathic thrombocytopenic purpura (ITP), and thrombotic thrombocytopenic purpura (TTP). However, in some cases, for example, cases
Yuhao Chen, Yuhao Chen, Lin Li, Jing Lu, Jing Lu   +4 more
doaj   +1 more source

Adult Idiopathic Thrombocytopenic Purpura

Hematology, 2003
Idiopathic thrombocytopenic purpura (ITP) in adults is an autoimmune disorder characterised by persistent thrombocytopenia due to autoantibodies directed against platelet antigens. There have been major advances in our understanding of the pathophysiology of ITP and an increasing number of diagnostic tests and treatments available.
Mead, A, Newland, A, Provan, D
openaire   +3 more sources

Manajemen Anestesi pada Seksio Sesarea dengan Idiopathic Thrombocytopenic Purpura: Serial kasus

Jurnal Anestesi Obstetri Indonesia, 2021
Trombositopenia merupakan perubahan hemostasis yang umum terjadi pada wanita hamil, namun jarang ditemukan kondisi berat. Idiopathic thrombocytopenic purpura (ITP) merupakan salah satu penyebab trombositopenia pada wanita hamil.
Achmad Haryanto, Ruddi Hartono, Isngadi Isngadi   +2 more
doaj   +1 more source

Post-Partum Thrombotic Thrombocytopenic Purpura (TTP) in a Patient with known Idiopathic (Immune) Thrombocytopenic Purpura: a case report and review of the literature

Journal of Medical Case Reports, 2018
BackgroundIncidences of immune thrombocytopenic purpura occur in 1 in every 1000–10,000 pregnancies accounting for 3% of all thrombocytopenic pregnancies.
Naser Al-husban, Oqba Al-kuran
semanticscholar   +1 more source

Immune Thrombocytopenia as a Consequence of Rocky Mountain Spotted Fever

Case Reports in Oncology, 2017
Primary immune thrombocytopenia (ITP) – also called idiopathic thrombocytopenic purpura or immune thrombocytopenic purpura – is an acquired thrombocytopenia caused by autoantibodies against platelet antigens.
Cherisse Baldeo, Karan Seegobin, Lara Zuberi   +2 more
doaj   +1 more source

Changes in Follicular Helper T Cells in Idiopathic Thrombocytopenic Purpura Patients

International Journal on Biological Sciences, 2015
Background: Idiopathic thrombocytopenic purpura (ITP) is a primary autoimmune disease with a decreased platelet count caused by platelet destruction mediated mainly by platelet antibodies. T follicular helper (TFH) cells have demonstrated important roles
Jue Xie, Da-Wei Cui, Yan Liu, Jie Jin, H. Tong, Lei Wang, Guo-Xiang Ruan, Yun-Bi Lu, Huiming Yuan   +8 more
semanticscholar   +1 more source

The Effects of Helicobacter pylori Eradication Therapy for Chronic Idiopathic Thrombocytopenic Purpura

Gut and Liver, 2015
Background/Aims The aim of this study was to evaluate the ability of Helicobacter pylori eradication treatment to increase platelet counts in Korean patients with chronic idiopathic thrombocytopenic purpura (ITP).
J. Hwang, Dong-Ho Lee, H. Yoon, C. Shin, Y. S. Park, Nayoung Kim   +5 more
semanticscholar   +1 more source

Type of plasma preparation used for plasma exchange and clinical outcome of adult patients with acquired idiopathic thrombotic thrombocytopenic purpura: a French retrospective multicenter cohort study

Transfusion, 2015
Plasma exchange (PE) is the first‐line therapy of acquired thrombotic thrombocytopenic purpura (TTP). Several plasma preparations have been available; their equivalence in terms of outcome remains uncertain.
M. Toussaint-Hacquard, P. Coppo, M. Soudant, L. Chevreux, S. Mathieu-Nafissi, T. Lecompte, Sylvie Gross, F. Guillemin, T. Schneider   +8 more
semanticscholar   +1 more source

Idiopathic thrombocytopenic purpura

Japanese Journal of Thrombosis and Hemostasis, 2008
Point（1）診断は血小板減少をきたす他の疾患の除外を基本とする．（2）血小板数と出血症状の程度，背景因子やライフスタイルに基づいて治療適応を決める．（3）治療はまずステロイド療法,次いで摘脾を行う．（4）ITPと診断されればまずH. pyloriを検索し，陽性であれば除菌療法を優先する．
openaire   +3 more sources

Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura

Haematologica, 2010
Background Type G immunoglobulins against ADAMTS13 are the primary cause of acquired (idiopathic) thrombotic thrombocytopenic purpura. However, the domains of ADAMTS13 which the type G anti-ADAMT13 immunoglobulins target have not been investigated in a ...
X. Long Zheng, Haifeng M. Wu, Dezhi Shang, Erica Falls, Christopher G. Skipwith, Spero R. Cataland, Charles L. Bennett, Hau C. Kwaan   +7 more
doaj   +1 more source