...Soo Min Ahn; Eun-Ji Choi; Ji Seon Oh; Yong-Gil Kim; Chang-Keun Lee; Bin Yoo; Seokchan Hong Introduction: We aimed to identify the clinical characteristics and risk factors for chronic immune thrombocytopenia (ITP) in patients with systemic lupus erythematosus (SLE). Methods: We retrospectively...

...Adi Sherban; Ragda Hussen; Anat Gafter-Gvili; Alla Atamna; Jihad Bishara; Pia Raanani; Kim Ben Tikva Kagan; Tomer Avni Introduction: Influenza virus causes significant global annual morbidity and mortality. Thrombocytopenia is recognized as a poor prognostic factor in sepsis and is associated...

... or acute myeloid leukemia and grade 4 thrombocytopenia (<25 × 10 9 platelets/L). Approximately 30–65% of patients in this open-label extension phase experienced clinically relevant thrombocytopenic events; no conclusions could be made regarding long-term efficacy (non-randomized design, no placebo...

...Marcel Kemper; Georg Lenz; Rolf Michael Mesters Vaccine-induced immune thrombotic thrombocytopenia (VITT) has already been described after vaccination with ChAdOx2 nCov-19 (AstraZeneca) and Ad26.COV2.S (Johnson & Johnson/Janssen). However, less knowledge so far has been gained about optimal...

... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Thrombocytopenia Anemia Leukopenia Thrombosis Thrombotic microangiopathy Rheumatic...

...Bora Son; Hee sue Park; Hye Sook Han; Hee Kyung Kim; Seung Woo Baek; Yaewon Yang; Ki Hyeong Lee; Jihyun Kwon Acquired amegakaryocytic thrombocytopenia (AAMT) is a rare disease that causes severe bleeding. The pathogenesis and treatment of AAMT have not yet been defined. We report the case of a 60...

... ALC, and platelet counts. Cox regression was used to analyze the risk factor for survival. Results: Patients with a higher eNLR (≥3), lymphopenia (< 1,000/μL), and thrombocytopenia (< 150 K/μL) had an inferior progression-free survival (PFS) and overall survival (OS) compared...

...; Kazuya Sato; Iekuni Oh; Ken Ohmine; Kazuo Muroi; Kentaro Ashizawa; Yu Yamamoto; Hisashi Oshiro; Yoshinobu Kanda TAFRO syndrome, a rare systemic inflammatory disease, can lead to multiorgan failure without appropriate treatment. Although thrombocytopenia is frequently seen in patients with TAFRO syndrome...

... Thrombocytopenia Platelet refractoriness Multitransfusion is a well-documented risk factor for the development of refractoriness to platelet transfusions [ 1 ]. Refractoriness to platelet transfusions has been reported to occur in 15-25% of hemato-oncological patients [ 1,2,3,4,5,6 ]. Poor response...

...Abdul Shlebak; Anthony Poles; Richard Manning; Shaikha Almuhareb; Josu De La Funte; Mike Mitchell; Geoff Lucas Background: Bernard-Soulier syndrome (BSS) is a congenital bleeding disorder characterised by thrombocytopenia, giant platelets and decreased platelet adhesion resulting from genetic...

... pseudothrombocytopenia in a consecutive outpatient population referred for isolated thrombocytopenia. Vox Sang 1995;68:35-39. 6. Lau LG, Chng WJ, Liu TC: Transfusion medicine illustrated. Unnecessary transfusions due to pseudothrombocytopenia. Transfusion 2004;44:801. 7. Zhou X, Wu X, Deng W, Li J, Luo W...

... (moderate bleeding including mucosal, not requiring intervention), 4 (severe bleeding including internal hemorrhage, requiring intervention), and 5 (life-threatening or fatal bleeding) [ 12 ]. To assess the bleeding risk, we analyzed a cohort of 300 patients with severe iatrogenic thrombocytopenia...

...Anders Møller; Ole Weis Bjerrum; Arash Afshari Background/Aims: Thrombocytopenia and the increasing use and variety of antithrombotic drugs is a challenge prior to lumbar puncture. This study examined the Danish haematology practice regarding drug pausation, assessment of haemostasis and whether...

... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Thrombocytopenia Sea-blue histiocytosis in bone marrow is a morphological finding that has been described...

... myosin 9-related disease (MYH9-RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thrombosis and Haemostasis 2010a;103:826-832. 7. Balduini CL, Pecci A, Savoia A: Recent advances in the understanding and management of MYH9 -related inherited thrombocytopenias. Br J...

...: Infectious causes of chronic immune thrombocytopenia. Hematol Oncol Clin North Am 2009;23:1275–1297. 2. Liebamn HA: Viral-associated immune thrombocytopenic purpura. Hematology Am Soc Hematol Educ Program 2008;212–218. 3. Al-Majed SA, Al-Momen AK, Al-Kassimi FA, Al-Zeer A, Kambal AM, Baaqil H...

...Hung Chang; Tzung-Chih Tang Acquired amegakaryocytic thrombocytopenia (AAMT) is an entity characterized by severe thrombocytopenia with a significantly reduced number of megakaryocytes in the bone marrow. AAMT is rare and poorly defined. Therefore, standard treatment is not well established...

... prominence to the periodical reevaluation of all the etiological hypotheses of thrombocytopenia in relation to its clinical condition. The majority of chronic ITP children do not require treatment, especially if bleeding is absent or minimal. The treatment decision depends on several factors other than...

... from any ideas, methods, instructions or products referred to in the content or advertisements. ADAMTS13 ADAMTS13 activity test Collagen binding assay Microthrombus formation Thrombocytopenia Thrombotic thrombocytopenic purpura (TTP) is a rare disease with an annual incidence...

...J. Polasek; F. Duckert Two patients with a known quinine induced allergic thrombocytopenia have been studied in order to detect in vitro the presence of drug-dependent antibodies in their plasma. The platelet factor 3 and platelet acid phosphatase availability tests have shown that these antibodies...