Results 91 to 100 of about 201,611 (277)

IgA Vasculitis: Etiology, Treatment, Biomarkers and Epigenetic Changes

open access: yesInternational Journal of Molecular Sciences, 2021
IgA, previously called Henoch-Schönlein vasculitis, is an essential immune component that drives the host immune response to the external environment.
Hitomi Sugino   +2 more
semanticscholar   +1 more source

Paraneoplastic IgA nephropathy and IgA vasculitis in mesothelioma [PDF]

open access: yesInternational Journal of Case Reports and Images, 2019
Immunoglobulin A (IgA) vasculitis and IgA nephropathy have been associated with underlying malignancies when present in adult populations. To date, we have found only two previously reported cases of IgA vasculitis and one IgA nephropathy case associated with mesothelioma, with our patient being the fourth.
Abendroth Catherine   +4 more
openaire   +2 more sources

Comparison and Analysis of Gut Microbiota in Children With IgA Vasculitis With Different Clinical Symptoms

open access: yesFrontiers in Pediatrics, 2022
Background: Henoch-Schönlein purpura, now called immunoglobulin A (IgA) vasculitis, is a common autoimmune disease in children, its association with gut microbiota composition remains unknown.
Meng Li   +6 more
semanticscholar   +1 more source

Expert Perspective: Diagnosis and Treatment of Castleman Disease

open access: yesArthritis &Rheumatology, Accepted Article.
Summary Castleman disease (CD) is a major diagnostic challenge for Rheumatologists. Unicentric CD (UCD) involves one enlarged lymph node region whereas multicentric CD (MCD) involves multiple enlarged lymph node regions. Both UCD and MCD may exhibit a wide range of symptoms that overlap with other immune‐mediated conditions.
Luke Y.C. Chen   +2 more
wiley   +1 more source

Pauci-immune glomerulonephritis in individuals with disease associated with levamisole-adulterated cocaine: a series of 4 cases. [PDF]

open access: yes, 2014
Exposure to levamisole-adulterated cocaine can induce a distinct clinical syndrome characterized by retiform purpura and/or agranulocytosis accompanied by an unusual constellation of serologic abnormalities including antiphospholipid antibodies, lupus ...
Butcher, Brad   +6 more
core   +2 more sources

Taxonomic and functional shifts of gut microbiome in immunoglobulin A vasculitis children and their mothers

open access: yesFrontiers in Pediatrics
ObjectivesTo examine the gut microbiota characteristics in children with immunoglobulin A vasculitis and their interrelationships with the host, while evaluate the vertical inheritance of microbiota in the development and progression of IgA vasculitis ...
Yijia Liang   +10 more
doaj   +1 more source

Neutrophil-to-lymphocyte ratio: A biomarker for predicting systemic involvement in iga vasculitis

open access: yesIndian Journal of Rheumatology, 2020
Context:“IgA vasculitis, is an immune complex mediated, self limited cutaneous small vessel vasculitis, characterized by palpable purpurae, arthralgia or arthritis, gastrointestinal and/or renal involvement.” Systemic involvement is considered to be the ...
Rintu Merin George   +2 more
doaj   +1 more source

Unilateral eyelid angioedema: An atypical manifestation in childhood IgA vasculitis

open access: yesIndian Journal of Paediatric Dermatology, 2023
Immunoglobulin A (IgA) vasculitis (Henoch–Schönlein purpura) is an immune-mediated small vessel vasculitis, in which edema of the nondependent areas of the body, including the face and scalp is a rare cutaneous finding, found mostly in children
R Deepashree   +1 more
doaj   +1 more source

Clinical impact of multiparametric contrast‐enhanced dual‐energy computed tomography in arthritis imaging – a prospective single‐center study

open access: yesArthritis &Rheumatology, Accepted Article.
Objectives To evaluate the influence of contrast‐enhanced dual‐energy CT (CE‐DECT) in detecting and differentiating rheumatic joint diseases of the hand. Methods In this prospective study, patients with suspected arthritis of the hand were investigated consecutively alongside the standard clinical procedure.
Sevtap Tugce Ulas   +9 more
wiley   +1 more source

Henoch–Schönlein Purpura (IgA Vasculitis) in Association with Thyrotoxicosis

open access: yesCase Reports in Endocrinology, 2021
Graves’ disease is the most common cause of hyperthyroidism, which is characterized by thyroid antibodies and the following clinical manifestations: goiter, ophthalmopathy, and pretibial myxedema.
Mojgan Sanjari   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy