Results 71 to 80 of about 8,451 (217)

Safety of Immune Checkpoint Inhibitors in Cancer Patients With Preexisting Autoimmune Vasculitis

ACR Open Rheumatology, Volume 8, Issue 3, March 2026.
Objective Immune checkpoint inhibitors (ICIs) are effective cancer therapies but often cause serious immune‐related adverse events (irAEs). Patients with preexisting autoimmune diseases, including vasculitis, are excluded from trials. We aimed to evaluate the frequency, severity, and outcomes of vasculitis flares and irAEs in this population.
Juan Sevillano, Noha Abdel‐Wahab, Yixuan Zhou, Juan I. Ruiz, Maria E. Suarez‐Almazor   +4 more
wiley   +1 more source

Fractional Microneedling Radiofrequency for Hidradenitis Suppurativa: A Real‐World Retrospective Study Demonstrating Clinical Efficacy and Safety Across Diverse Anatomical Sites

Journal of Cosmetic Dermatology, Volume 25, Issue 3, March 2026.
ABSTRACT Background Hidradenitis suppurativa (HS) remains a therapeutically challenging disease despite expanding research and evolving systemic treatments. Energy‐based modalities, such as fractional microneedling radiofrequency (FMR), are being increasingly explored as novel treatment options.
Ari Safir, Eyal Taleb, Daniella Berzin, Manny Arieli, Aspasia Liassidou, Waseem Shehadeh, Ariela Hafner, Ofir Artzi   +7 more
wiley   +1 more source

Diagnostic challenge of intestinal obstruction secondary to Henoch–Schonlein purpura [PDF]

, 2018
Henoch–Schonlein purpura is the most common form of vasculitis in pediatric age group. Gastrointestinal manifestations have been long recognized as part of the disease, but usually preceded by other manifestations.
Ahmed, Ali M., Al-Shahrani, Mohammad S., Aljubab, Abdulwahab S.   +2 more
core   +2 more sources

Successful Treatment of Severe Purpura Fulminans With Anakinra

Pediatric Dermatology, Volume 43, Issue 2, Page 421-424, March/April 2026.
ABSTRACT Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities.
Francesco Zulian, Luca Spiezia, Antonio Amabile, Francesca Tirelli, Alessandra Meneghel   +4 more
wiley   +1 more source

Increased Serum Interleukin-17 and Peripheral Th17 Cells in Children with Acute Henoch-Schonlein Purpura [PDF]

, 2012
Background: Interleukin (IL)-17 and Th17 cells have been involved in many autoimmune diseases. The aim of this study is to investigate the involvement of IL-17 and Th17 cells in the pathogenesis of childhood Henoch-Schonlein purpura (HSP ).
JEN, HSIAO-YU;CHUANG, YA-HUI;LIN, SHENG-CHIEH;CHIANG, BOR-LUEN;YANG, YAO-HSU, 任曉玉;莊雅惠;林聖捷;江伯倫;楊曜旭   +1 more
core  

Association of Mycoplasma Pneumoniae Infection with Henoch-Schonlein Purpura [PDF]

, 2013
We present a  child with Henoch-Schonlein purpura and Mycoplasma pneumoniae infection, an association that was rarely described in  the literature.
Sharifi, Fariba,  A. Voutsioti, M. Moustaki, Yiallouros, Panayiotis K., Voutsioti, Aikaterini, Karpathios, Themistocles, Moustaki, Maria, Themistocles Karpathios, P. Yiallouros, F. Sharifi   +9 more
core   +1 more source

Pulmonary haemorrhage and pleural effusion in an elderly patient with Henoch-Schönlein purpura (IgA vasculitis)-: a case report

Journal of the Pakistan Medical Association
Henoch-Schönlein purpura (HSP) also known as IgA vasculitis is a systemic small vessel vasculitis mainly affecting the skin, kidneys, joints, and gastrointestinal tract. However, the disease can affect any organ system of the body. The classic tetrad of
Muhammad Tahir, Muhammad Zuhair Tahir, Muhammad Zubair Tahir, Ayesha Salim   +3 more
doaj   +1 more source

Risk Factors of Disease Progression in IgA Nephropathy: A Systematic Review and Meta‐Analysis

Immunity, Inflammation and Disease, Volume 14, Issue 2, February 2026.
ABSTRACT Objective IgA nephropathy (IgAN) is an important cause of chronic renal failure, and nearly all patients with IgAN are at risk of developing to end‐stage renal disease (ESRD) during their lifetime. This meta‐analysis aimed to identify and evaluate risk factors associated with the progression of IgAN patients.
Dan Xu, Minjie Zhang, Weiwei Liang, Lijiang Fang, Feifei Ge   +4 more
wiley   +1 more source

Henoch–Schonlein purpura antecedent to Crohn’s disease [PDF]

, 2015
We report a 13-year-old youth who initially presented with the typical rash of Henoch–Schonlein purpura followed a month later by a nephrotic syndrome and hematuria. Renal biopsy revealed crescentic IgA nephropathy.
Tania Zehavi, Yosef Uziel, Galit Pomeranz, Ze’ev Korzets, Avishalom Pomeranz   +4 more
core   +1 more source

New‐onset autoimmune disease following SARS‐CoV‐2 infection and mRNA vaccination in Norway: A retrospective cohort study

Journal of Internal Medicine, Volume 299, Issue 2, Page 271-282, February 2026.
Abstract Background Studies suggest an increase in autoimmune diseases following SARS‐CoV‐2 infection and/or COVID‐19‐vaccination. We aimed to describe possible associations in Norway. Methods We used information from the emergency preparedness register for COVID‐19, BeredtC19, for all residents aged 18–64 (N = 3,450,080).
Håkon Bøås, Paz Lopez‐Doriga Ruiz, Jesper Dahl, Hanne L. Gulseth, German Tapia   +4 more
wiley   +1 more source