Results 31 to 40 of about 6,906 (205)
Pulmonary involvement in Henoch-Schonlein purpura [PDF]
A 72-year-old man presented to the emergency department with a 2-day history of fever and difficulty in breathing. His medical history included Henoch–Schonlein purpura treated with steroids, pulmonary tuberculosis treated with antimicrobials, and lobectomy of the right …
Andreas Soloukides+3 more
openaire +3 more sources
The review discusses peculiarities of secondary IgA-nephropathy, complicating Henoch–Schonlein purpura,spondyloarthropathies, gluten enteropathy HCV infections, AIDS, liver cirrhosis, hereditary nephritis.
A. Yu. Nikolaev, A. V. Malkoch
doaj
Circulating Fetuin‐A concentrations in rheumatic diseases: a systematic review and meta‐analysis
In this systematic review with meta‐analysis, we identified 19 eligible studies to determine whether there is any change in Fetuin‐A (FtA) concentrations in patients with rheumatic diseases. We observed a significant decrease in FtA concentrations in RD patients (standardized mean difference, SMD = −.91; 95% CI −1.43 to −.39, p = .001).
Biagio Di Lorenzo+6 more
wiley +1 more source
Bullous Henoch–Schonlein purpura with involvement of face
Henoch–Schonlein purpura (HSP) with facial involvement with bullous rashes are extremely rare. A 12-year-old boy presented with abdominal pain and features of arthritis. He also had multiple purpuric rashes over his lower limbs.
Devdeep Mukherjee+4 more
doaj +1 more source
A mechanistic model of the pathogenic role of urinary exosomal miRNAs in IgA vasculitis nephritis via pro‐fibrotic and inflammatory pathways. IgAV: IgA vasculitis. IgAVN: IgA vasculitis nephritis [Figure created with BioRender.com]. Abstract This study aimed to comprehensively evaluate the diagnostic potential of urinary exosomal microRNA (miRNA) in ...
Yunfan Zhang+14 more
wiley +1 more source
ABSTRACT Background and Aims Drug‐induced renal vasculitis arises from various medications that cause immunological dysregulation or direct vascular damage, leading to inflammation and thrombosis. Clinical manifestations vary widely, from mild constitutional symptoms to severe organ dysfunction. This review aims to thoroughly explore drug‐induced renal
Hashim Mohamed Siraj+7 more
wiley +1 more source
Summary Background In immune complex vasculitis the detection of perivascular immunoglobulins by direct immunofluorescence (DIF) not only helps to confirm the diagnosis, but also to define the type of vasculitis (e.g., IgA‐, IgG/IgM‐, rheumatoid or cryoglobulinemic vasculitis).
Luisa Herda+2 more
wiley +1 more source
Applications of Artificial Intelligence in Vasculitides: A Systematic Review
Objective Vasculitides are rare inflammatory disorders that sometimes can be difficult to diagnose due to their diverse presentations. This review examines the use of artificial intelligence (AI) to improve diagnosis and outcome prediction in vasculitis.
Mahmud Omar+6 more
wiley +1 more source
This research study provides a comparison of the diagnostic performance of urinary red blood cell distribution (URD) and dysmorphic RBC (dRBC) in a multicenter study. ABSTRACT Background The clinical utility of urinary red blood cell (RBC) distribution (URD) remains limited.
A‐Jin Lee+7 more
wiley +1 more source
This Mendelian randomization (MR) analysis aimed to assess the causal relationship between the Herpes virus (HSV, herpes simplex virus; HHV‐6, human herpesvirus 6; VZV, varicella‐zoster virus; CMV cytomegalovirus; EBV, Epstein‐Barr virus) and leukocytoclastic angiitis.
Heyi Zhang+10 more
wiley +1 more source