Results 51 to 60 of about 17,788 (263)

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

Therapeutic advances in the treatment of vasculitis [PDF]

open access: yes, 2016
Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core   +2 more sources

A Review of IgA Vasculitis (Henoch-Schönlein Purpura) Past, Present, and Future

open access: yesMedical Science Monitor
The clinical association of purpura, arthralgia, and arthritis was first described in 1837 in a publication by Johann Lukas Schönlein, a German physician.
D. Parums
semanticscholar   +1 more source

Henoch-Schönlein purpura with intracerebral haemorrhage in an adult patient: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Henoch-Schönlein purpura is a small vessel vasculitis that affects mainly the skin, joints, gastrointestinal tract and kidneys. The central nervous system is also occasionally affected, although the majority of patients experience only mild ...
Karamadoukis Lazarus   +2 more
doaj   +1 more source

Acute Hemorrhagic Edema of Infancy [PDF]

open access: yes, 2016
Acute Hemorrhagic Edema of Infancy is a small vessel leucocytoclastic vasculitis affecting young infants. It is characterized by large, target-like, macular to purpuric plaques predominantly affecting the face, ear lobes and extremities.
Amaro, C   +3 more
core   +1 more source

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

Different histological classifications for Henoch-Schönlein purpura nephritis: which one should be used?

open access: yesPediatric Rheumatology Online Journal, 2019
BackgroundNephritis is the most important chronic complication of IgA Vasculitis (IgAV)/Henoch-Schönlein purpura (IGAV/HSP) and thus the main prognostic factor of this most common childhood vasculitis.
M. Jelušić   +3 more
semanticscholar   +1 more source

Henoch-Schonlein Purpura

open access: yesPediatric Care Online, 2020
Key Points Henoch-Schönlein purpura (HSP) is the most common form of vasculitis in children.It is a small-vessel vasculitis mediated by immunoglobulin A–containing immune complexes and characterized by nonthrombocytopenic purpura, abdominal pain, arthralgia, and renal disease.Diagnosis of HSP is clinical, and no laboratory tests are ...
openaire   +2 more sources

Higher complement C4 gene copy number constitutes a shared genetic risk factor for giant cell arteritis and IgA vasculitis

open access: yesArthritis &Rheumatology, Accepted Article.
Objective Low copy number (CN) of complement C4 isoforms and high CN of retroviral HERV‐K elements are known risk factors for many immune‐mediated inflammatory diseases (IMIDs), often showing sex‐biased effects. Here, we assessed whether CN variation within the C4 gene contributes to giant cell arteritis (GCA) and IgA vasculitis (IgAV), two complex ...
Laura Martínez‐Gutiérrez   +296 more
wiley   +1 more source

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