ALLMedicine™ Purpura Center
Research & Reviews 3,264 results
Expert Review of Hematology; Jain N, Oldenburg J et. al.
Jun 25th, 2022 - Hemophilia, von Willebrand disease (VWD), and thrombotic thrombocytopenic purpura (TTP) are rare diseases affecting normal hemostasis. Although they differ in their pathogenesis and clinical manifestation, if left undiagnosed and untreated, all th...
https://doi.org/10.1186/s13023-022-02400-y 10.1002/pbc.24612 10.1111/j.1538-7836.2005.01436.x 10.1186/s13023-019-1240-0 10.1111/j.1365-2141.2008.07276.x 10.1016/S2352-3026(16)30018-7 10.3324/haematol.2018.198275 10.1182/blood-2009-09-243790 10.1055/s-0034-1395154 10.1111/j.1365-2141.2010.08385.x 10.1371/journal.pone.0033029 10.1007/s12185-011-0771-5 10.1111/imj.12935 10.1111/jth.12790 10.1007/s11684-016-0492-5 10.1111/jth.12826 10.1182/bloodadvances.2017005124 10.1002/jca.21510 10.1111/jth.13571 10.1111/jth.15006 10.1016/j.transci.2020.102990 10.1111/ijlh.13295 10.1002/jca.21470 10.1371/journal.pone.0010208 10.1111/bjh.13658 10.1016/S2352-3026(17)30026-1 10.1111/vox.12912
Orphanet Journal of Rare Diseases; Mancini I, Agosti P et. al.
Jun 24th, 2022 - Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy (TMA) requiring urgent treatment. Standardization of its diagnosis and optimal management is challenging. This study aimed to evaluate the role of cen...
Journal of Clinical Apheresis; Kohli R, Geneen LJ et. al.
Jun 22nd, 2022 - The aim of this systematic scoping review is to identify and categorize the outcome measures that have been reported in clinical studies, where therapeutic plasma exchange (TPE) has been used as an intervention in any clinical settings, excluding ...
BMJ Case Reports; Koilpillai S, Dominguez B et. al.
Jun 21st, 2022 - Immune thrombocytopenic purpura (ITP) is an autoimmune disorder caused by autoantibodies against platelet antigens resulting in platelet destruction and inhibition of platelet production. Occasionally, an inciting event such as a virus or vaccinat...
https://doi.org/10.1007/s10067-022-06181-4 10.1016/j.revmed.2013.12.004 10.1016/j.autrev.2017.10.009 10.1053/sarh.2000.6988 10.1111/1346-8138.14466 10.1111/jdv.14683 10.1038/sj.leu.2404284 10.1002/art.40178 10.1016/j.autrev.2020.102611 10.1016/j.kint.2016.10.026
Clinical Rheumatology; Hankard A, Ingen-Housz-Oro S et. al.
Jun 18th, 2022 - There is currently no evidence of the possible benefit of plasma cell-targeting therapies (PCTT) in immunoglobulin A (IgA) monoclonal gammopathy (MG) associated with IgA vasculitis (IgAV). We report the outcome of different PCTT regimens in a coho...
Guidelines 5 results
British Journal of Haematology; Allar BG, Michaelsen K et. al.
Aug 6th, 2020 - Oropharyngeal psychogenic purpura.|2020|Allar BG,Michaelsen K,Gupta A,Bose S,|metabolism,pathology,metabolism,pathology,metabolism,pathology,metabolism,pathology,metabolism,pathology,
Rheumatology (Oxford, England); Ozen S, Marks SD et. al.
Mar 18th, 2019 - IgA vasculitis (IgAV, formerly known as Henoch-Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date, there are no internationally agreed, evidence-based guidelines concerning the appropriate diagnosis and treatm...
The American Journal of Gastroenterology; Chey WD, Leontiadis GI et. al.
Jan 11th, 2017 - Helicobacter pylori (H. pylori) infection is a common worldwide infection that is an important cause of peptic ulcer disease and gastric cancer. H. pylori may also have a role in uninvestigated and functional dyspepsia, ulcer risk in patients taki...
British Journal of Haematology; Scully M, Hunt BJ et. al.
May 26th, 2012 - Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies.|2012|Scully M,Hunt BJ,Benjamin S,Liesner R,Rose P,|diagnosis,pathology,therapy,diagnosis,pathology,therapy,
British Journal of Haematology; Levi M, Toh CH et. al.
Feb 19th, 2009 - The diagnosis of disseminated intravascular coagulation (DIC) should encompass both clinical and laboratory information. The International Society for Thrombosis and Haemostasis (ISTH) DIC scoring system provides objective measurement of DIC. Wher...
Drugs 387 results see all →
Clinicaltrials.gov 254 results
Jun 14th, 2022 - Systemic lupus erythematosus (SLE) is a systemic heterogeneous autoimmune disease with a highly variable course and prognosis that many different organs may be affected . It has wide spectrum of clinical presentation that affects all ages and ethn...
Jun 8th, 2022 - The Part A of the study is currently not accepting healthy volunteers as the recruitment for the part A has completed.
May 27th, 2022 - The lack of ADAMTS13 is the only biological marker that is specific for aTTP diagnosis8 and the assessment of ADAMTS13 is of clinical importance because it is essential for the rapid differential diagnosis between aTTP and other TMA. Furthermore, ...
May 24th, 2022 - 1.) Identification of predictive markers for morbidity and mortality in acute TTP and in TTP relapses using a prospective long-term registry and 2.) Investigation of the pathophysiological processes in acute bouts and in remission by recording the...
May 12th, 2022 - In recent years the critical role of miRNAs has been established in many diseases, including autoimmune disorders. Immune thrombocytopenic purpura (ITP) is a predominant autoimmune disease, in which aberrant expression of miRNAs has been observed,...
News 409 results
MDedge Family Medicine;
May 26th, 2022 - Since the papules were worrisome for vasculitis, 2 punch biopsies were performed on smaller, younger lesions on the hand and 1 was submitted for direct immunofluorescence. Findings revealed a leukocytoclastic vasculitis (LCV) with prominent immuno.
Mark C. Marchitto, MD, Liesl Grenier, MD et. al.
May 10th, 2022 - The Diagnosis: Calciphylaxis Histopathology revealed epidermal and dermal necrosis, a perivascular neutrophilic infiltrate, and scattered microcalcifications within small- and medium-sized subcutaneous vessels, consistent with a diagnosis of calci.
Lynette Xu, Brooke Resh Sateesh, MD
Apr 19th, 2022 - Purpura annularis telangiectodes of Majocchi (PATM) or Majocchi’s disease, is an uncommon subtype of pigmented purpuric dermatosis (PPD) or capillaritis, typically characterized by symmetrical, nonblanching, purpuric, telangiectatic, and atrophic.
MDedge Family Medicine;
Apr 14th, 2022 - A punch-biopsy was performed on the left second toe where the erythema was the most intense. It demonstrated classic findings for pernio: superficial and deep perivascular lymphocytic inflammation and papillary dermal edema on the acral surface.
Katherine G. Beuerlein, BS, Elise D. Martin, MD et. al.
Mar 3rd, 2022 - The number of monoclonal antibodies developed for therapeutic use has rapidly expanded over the last decade due to their generally favorable adverse effect (AE) profiles and efficacy. 1 Tumor necrosis factor α inhibitors and general integrin antago.