Results 31 to 40 of about 8,427 (168)

Clinical Study Outcome Indicators for Henoch-Schonlein Purpura Nephritis: a Scoping Review [PDF]

open access: yesZhongguo quanke yixue
Background Henoch-Schonlein purpura is a vascular inflammatory illness that develops in childhood and in some children involves the kidneys, clinically known as Henoch-Schonlein purpura nephritis. Different studies have suggested different interventions,
TONG Jinghan, WU Xiaoming, SUN Yaxin, LI Shuning, LIANG Chen, DONG Heng, CHE Gang, LIU Chang, HU Yan, LIU Yali
doaj   +1 more source

Henoch-Schönlein purpura with c-ANCA antibody in an adult [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
: The Henoch-Schönlein purpura is the vasculitis associated with deposits of immunoglobulin A in small vessels. Its association with cytoplasmic antineutrophil cytoplasmic antibodies is possible, but rare.
Pedro de Freitas Silva Torraca   +2 more
doaj   +2 more sources

A rare association of invasive infective endocarditis due to Abiotrophia defectiva with ventricular septal defect and recurrent Henoch-Schonlein purpura in a child

open access: yesJournal of Cardiothoracic Surgery, 2022
Background Henoch-Schonlein purpura is the most common vasculitis in childhood, usually triggered by an upper respiratory tract infection and rarely observed in infective endocarditis patients. Abiotrophia defectiva is a rare causative agent of infective
Wenpeng Dong, Shuibi Wu, Jing Zhou
doaj   +1 more source

New-Onset Henoch–Schonlein Purpura after COVID-19 Infection: A Case Report and Review of the Literature

open access: yesCase Reports in Pediatrics, 2022
Extrapulmonary manifestations of COVID-19 infection include a wide spectrum of cutaneous, endocrine, and cardiovascular complications. We report three cases of new-onset Henoch–Schonlein purpura (HSP) in COVID-19 infected children that were diagnosed and
Ashwag Asiri   +3 more
doaj   +1 more source

Exercise‐Induced Vasculitis in a 12‐Year‐Old Child: A Case Report

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Exercise‐induced vasculitis (EIV), colloquially known as “Disney rash,” is a benign, self‐limited leukocytoclastic vasculitis of the lower extremities triggered by prolonged exertion in warm weather, well‐recognized in adults but underappreciated in children.
Beverly X. Yu   +3 more
wiley   +1 more source

Púrpura de henoch-schonlein: revisão bibliográfica e relato de um caso. [PDF]

open access: yes, 1998
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Minatto, André Caporal
core  

PECU: A multicenter study on pediatric patients with cold‐induced urticaria

open access: yesPediatric Allergy and Immunology, Volume 37, Issue 6, June 2026.
Abstract Background Cold‐induced urticaria (ColdU) is a rare chronic inducible urticaria that can cause systemic reactions, including cold‐induced anaphylaxis (ColdA), but pediatric data are limited. The aim of this study was to evaluate the clinical characteristics, comorbidities, management approaches, risk of anaphylaxis, and long‐term course of ...
Betul Gemici Karaaslan   +59 more
wiley   +1 more source

GloPath: An Entity‐Centric Foundation Model for Glomerular Lesion Assessment and Clinicopathological Insights

open access: yesAdvanced Science, Volume 13, Issue 29, 22 May 2026.
An entity‐centric foundation model, GloPath, is introduced for comprehensive glomerular lesion assessment from routine renal biopsy images. Trained on over one million glomeruli, the framework enables robust lesion recognition, grading, and cross modality diag nosis, while uncovering large‐scale clinicopathological associations.
Qiming He   +28 more
wiley   +1 more source

Biologics and Drug‐Induced Immunogenicity: A Case Report of Acquired Hemophilia A Presenting After Immunotherapy

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Acquired hemophilia A is a rare, potentially life‐threatening bleeding disorder caused by autoantibody inhibitors to coagulation factor VIII. We report the case of an 87‐year‐old female who presented with symptomatic bleeding and was subsequently diagnosed with acquired hemophilia A.
Kevin A. Murgas   +4 more
wiley   +1 more source

Telitacicept Combined With Glucocorticoids as Initial Therapy for Moderate IgA Vasculitis Nephritis With Concurrent Pulmonary Infection in Children: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
This graphical abstract depicts the clinical course of a 14‐year‐old male with moderate IgAV‐N treated with telitacicept combined with glucocorticoids as initial therapy. Rapid glucocorticoid tapering, normalized renal function, and continuous remission of proteinuria and hematuria were achieved.
Jiayi Li   +7 more
wiley   +1 more source

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