Results 21 to 30 of about 58,192 (237)
Henoch-Schönlein purpura with acute pancreatitis: analysis of 13 cases
BMC Pediatrics, 2018 Background Henoch-Schönlein purpura is a common small vessel vasculitis in children. Acute pancreatitis rarely presents as a complication of Henoch-Schönlein purpura and has not been well characterized.
Qin Zhang +6 more
doaj +1 more source
Púrpura de Schönlein-Henoch asociada a infección por Helicobacter pylori
, 2023 La púrpura de Schönlein-Henoch una vasculitis causada por mecanismo inmunológico frecuente en niños varones de 3 a 15 años. Se caracteriza por una púrpura palpable, artritis o artralgias, dolor cólico abdominal o hemorragia gastrointestinal y nefritis ...
Belaunde Clausell, Antonio +3 more
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Esplenectomia na púrpura trombocitopênica imunológica crônica em crianças [PDF]
, 2011 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Otani, Flávia Helena
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Severe Thrombocytopenia With Wet Purpura in Brucellosis: A Case Report. [PDF]
Clin Case RepABSTRACT Brucellosis is a zoonotic infection that passes to humans from infected animals via direct contact or the intake of raw milk and its products. The hematologic profile most frequently seen in acute brucellosis includes mild anemia and leukopenia. Severe form of thrombocytopenia and multiple wet purpura over the tongue and buccal mucosa are less
Ravanbakhsh Ghavghani F +2 more
europepmc +2 more sources
AGING MEDICINE, EarlyView.This 20‐year retrospective study reveals a significant increase in renal biopsy utilization and a pivotal shift in biopsy‐proven renal disease among Chinese elderly patients. Secondary glomerular nephropathy (particularly diabetic nephropathy and hypertensive nephropathy) has surpassed primary glomerular nephropathy as the leading biopsy‐proven ...
Shasha Han +4 more
wiley +1 more source
Henoch-Schonlein Purpura (HSP)
Keluwih, 2019 —Henoch-Schonlein purpura (HSP) is a systemic vasculitic disease (vascular inflammation) characterized by the deposition of immune complexes consisting of IgA in kidney skin.
Lucia Pudyastuti Retnaningtyas
doaj +1 more source
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 +4 more
doaj +1 more source
American Journal of Hematology, EarlyView.ABSTRACT Limited data exist on how patients and physicians perceive immune thrombocytopenia (ITP) symptoms and treatment‐related burden. I‐WISh (ITP World Impact Survey) 2.0 surveyed 1018 patients and 431 physicians in 15 countries to characterize the impact of ITP and its treatments on patients.
Nichola Cooper +17 more
wiley +1 more source
Novel Mutation of Upshaw-Schulman Syndrome Associated with Coarctation of Aorta in Palestinian Child [PDF]
Ķazaķstannyṇ Klinikalyķ Medicinasy, 2020 Upshaw-Schulman syndrome is a rare inherited form of thrombotic thrombocytopenic purpura disease caused by deficiency of ADAMTS13 and reversible by fresh frozen plasma infusions.
Mahdi Zaid +5 more
doaj +1 more source
Arthritis &Rheumatology, EarlyView.Sjögren disease (SjD) is a common systemic autoimmune disorder characterized by inflammation of the exocrine glands, resulting in dryness. Patients frequently exhibit extraglandular manifestations affecting various organ systems. To date, there are no US Food and Drug Administration (FDA)‐approved disease‐modifying therapies for SjD. In this review, we
Rachael A. Gordon, Sara S. McCoy
wiley +1 more source