ALLMedicine™ Purpura Center
Research & Reviews 2,734 results
https://doi.org/10.1186/s13256-022-03388-6 10.1016/s0037-1963(00)90106-9 10.1182/blood-2012-08-448944 10.1056/NEJMoa1802897 10.1056/NEJM199411033311807 10.1111/j.1423-0410.1987.tb03029.x 10.3324/haematol.2016.161968 10.3390/ijms18020441
Journal of Medical Case Reports; Sugiura T, Fujiwara A et. al.
May 14th, 2022 - Gaucher disease is an autosomal recessive inborn error of metabolism that causes disorders of blood, bone, and central nervous system as well as hepatosplenomegaly. We present the case of a carrier of Gaucher disease with gestational thrombocytope...
https://clinicaltrials.gov/ct2/show/NCT05371743
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,...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060716
Thrombosis Research; Saluja P, Gautam N et. al.
May 10th, 2022 - With the advent of COVID-19 vaccines, hospitalization rates and progression to severe COVID-19 disease have reduced drastically. Most of the adverse events reported by the vaccine recipients were minor. However, autoimmune hematological complicati...
https://doi.org/10.1016/j.chest.2021.12.632
Chest Singh J, Randev S et. al.
May 9th, 2022 - A 16-year-old girl presented to the ED with complaints of loose stools, abdominal pain, and rash over her legs for the last 7 days. There was no history of fever, vomiting, oral ulcers, or mucosal bleeds. In the past, she had received a diagnosis ...
https://doi.org/10.1007/s10067-022-06155-6 10.1182/blood-2016-10-709857 10.1056/NEJMicm1813768 10.3389/fimmu.2021.757192 10.1016/S0140-6736(19)30237-5 10.1093/rheumatology/ken510 10.1177/0961203308094360 10.1186/s13023-020-01510-9 10.12659/ajcr.898955 10.1186/s13052-019-0641-y 10.1182/blood.2019000954 10.1177/0961203320953473 10.1056/NEJMoa1806311 10.1182/blood.2020008021 10.1016/j.autrev.2020.102736 10.1007/s40265-018-0872-z 10.1038/nrdp.2016.39 10.1111/jth.13571 10.1093/rheumatology/keq395 10.1056/NEJMra1312353 10.1182/blood-2018-02-791533 10.1159/000441107 10.1146/annurev-immunol-042718-041717 10.1038/s41590-018-0120-4 10.3109/0886022X.2014.934649 10.2215/CJN.01480308 10.1007/s10067-013-2312-5 10.1097/MOH.0000000000000602 10.1016/j.autrev.2014.01.004 10.1111/bjh.18040 10.1016/j.ebiom.2018.12.035 10.1002/14651858.CD010668.pub2 10.1002/art.34400 10.1111/cei.12472 10.1111/1744-9987.13807 10.3324/haematol.2019.s1 10.1182/blood.V108.11.3993.3993
Clinical Rheumatology; Liang SJ, Zheng QY et. al.
May 8th, 2022 - Thrombotic thrombocytopenic purpura (TTP), a life-threatening syndrome characterized by acute microangiopathic hemolytic anemia, thrombocytopenia, and visceral ischemia, can be classified as congenital TTP (inherited due to a mutation in ADAMTS13)...
Guidelines 5 results
https://doi.org/10.1111/bjh.17021
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,
https://doi.org/10.1093/rheumatology/kez041
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...
https://doi.org/10.1038/ajg.2016.563
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...
https://doi.org/10.1111/j.1365-2141.2012.09167.x
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,
https://doi.org/10.1111/j.1365-2141.2009.07600.x
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 379 results see all →
Clinicaltrials.gov 79 results
https://clinicaltrials.gov/ct2/show/NCT05371743
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,...
https://clinicaltrials.gov/ct2/show/NCT05360251
May 4th, 2022 - Rosacea is a chronic skin condition characterized by erythema, inflammatory papules, pustules and telangiectasias, which typically occur on the face of middle-aged adults, especially fair skinned. The disease can lead to social stigmatization and ...
https://clinicaltrials.gov/ct2/show/NCT05360134
May 4th, 2022 - This project is a pilot randomized controlled trial aimed at investigating the potential of Carica Papaya Leaf Extract, available in a marketed pill formulation, in increasing platelet counts in live donor liver transplant recipients. Carica Papay...
https://clinicaltrials.gov/ct2/show/NCT01891994
Apr 12th, 2022 - Severe aplastic anemia (SAA) is a life-threatening blood disease that can be successfully treated with immunosuppressive drug regimens or allogeneic stem cell transplantation. However, 20-40% of patients are ineligible for transplant due to lack o...
https://clinicaltrials.gov/ct2/show/NCT05324618
Apr 12th, 2022 - Atopic dermatitis is a common pruritic inflammatory skin disorder. The prevalence of atopic dermatitis increased in the last three decades by two or three folds worldwide. In the developed countries, atopic dermatitis is estimated to affect 15% to...
News 281 results
https://www.mdedge.com/familymedicine/article/253770/dermatology/case-cold-purple-toes
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.
https://www.mdedge.com/dermatology/article/252140/dermatopathology/leukemia-cutis-manifesting-nonpalpable-purpura
Julianne Clowry, MB, BCh, BAO, Laura Nestor, MB, BCh, BAO et. al.
Feb 24th, 2022 - To the Editor: A 72-year-old man presented with symptomatic anemia and nonpalpable purpura of the legs, abdomen, and arms of 2 weeks’ duration (Figure 1). There were no associated perifollicular papules.
https://www.onclive.com/view/key-takeaways-from-discussion
Feb 23rd, 2022 - Caroline Piatek, MD: An important takeaway is that ITP is a heterogeneous disorder. There are different ways to treat it in the up-front and relapsed setting, so there’s no right way to do it. As we look at new and immersion therapies, we’re findi...
https://www.onclive.com/view/experimental-agents-for-itp
Feb 23rd, 2022 - Craig Kessler, MD: Sutimlimab is a humanized monoclonal antibody that selectively inhibits activation of the complement pathway by binding to complement 1S. This drug, which is not approved, will be marketed by Sanofi. It was originally developed ...
https://www.onclive.com/view/treatment-of-older-patients-with-itp
Feb 9th, 2022 - James Bussel, MD: Craig, you promised to share your wisdom about how to manage the older patients with ITP [immune thrombocytopenic purpura] because there are changes in responses and especially adverse effects for some of the treatments we might ...