Results 81 to 90 of about 17,788 (263)

Fibromatous periorchitis [PDF]

open access: yes, 2009
We report a case of diffuse fibrous pseudotumour/fibromatous periorchitis, in a 43 year old male, that completely encased the right testis and was adjacent to a hydrocoele cavity.
Barakzai, Abrar   +2 more
core   +1 more source

Comprehensive multi‐omics mapping of immune perturbations in autism spectrum disorder

open access: yesClinical and Translational Medicine, Volume 15, Issue 12, December 2025.
• Integrated multi‐omics profiling reveals systemic immune dysregulation in ASD, marked by an expansion of atypical immune cell subsets and activation of immune‐related pathways. • Significant alterations in peripheral immune cell populations are observed, including dysregulated NK cells, expanded CD56+ monocytes, and elevated MDSCs, and these changes ...
Chun Yan   +12 more
wiley   +1 more source

Incidence and risk factors for recurrent Henoch-Schönlein purpura in children from a 16-year nationwide database

open access: yesPediatric Rheumatology Online Journal, 2018
BackgroundThe recurrence rate of Henoch-Schönlein purpura (HSP) is 2.7%–30%, with varied average intervals between the first and second episodes.
Wei‐Te Lei   +8 more
semanticscholar   +1 more source

Continuous Exposure to Environmental Endocrine Disruptors on the Prognosis of Children With Nephritis: An Observational Cohort Study

open access: yesReproductive, Female and Child Health, Volume 4, Issue 4, December 2025.
ABSTRACT Objective Explore the impact of partial urinary environmental endocrine disruptors (EEDs) on the pathogenesis and renal function in paediatric patients diagnosed with Henoch‐Schönlein purpura nephritis (HSPN). Methods This was an observational cohort study.
Hongjun Peng   +6 more
wiley   +1 more source

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

open access: yesJournal 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   +3 more
doaj   +1 more source

Anastrozole-related acute hepatitis with autoimmune features: a case report [PDF]

open access: yes, 2011
Background Two cases of acute hepatitis occurring during treatment with anastrozole have previously been reported, but the underlying mechanisms of liver injury are still uncertain.
Alessandro Inno   +7 more
core   +2 more sources

Incidence of Autoimmune Diseases in 30,340 Danish Women With Polycystic Ovary Syndrome (PCOS) Compared to 151,520 Controls. A National Cohort Study

open access: yesClinical Endocrinology, Volume 103, Issue 6, Page 863-872, December 2025.
ABSTRACT Objective Autoimmunity can be part of the pathogenesis of polycystic ovary syndrome (PCOS), but prospective studies on autoimmune disease in population based cohorts are lacking. This study aimed to investigate incidence rates of autoimmune disease in Danish women with PCOS before and after PCOS diagnosis compared to controls.
Dorte Glintborg   +4 more
wiley   +1 more source

Adult-Onset Henoch-Schonlein Purpura Duodenitis

open access: yesJournal of Clinical Medicine Research, 2017
Henoch-Schonlein purpura (HSP) is an immune-mediated vasculitis. HSP presents with purple spots on the skin (purpura), arthralgia, digestive problems, and kidney injury. HSP is most commonly seen in children, and rarely presents in adults. The pathogenesis involves the deposition of immune complexes in small to medium size blood vessels which leads to ...
Ofori, Emmanuel   +4 more
openaire   +3 more sources

Collapsing Glomerulopathy in Brazil: A Nationwide Descriptive Study

open access: yesNephrology, Volume 30, Issue 12, December 2025.
This multicenter study describes the characterization and outcomes of a retrospective cohort of collapsing glomerulopathy cases conducted in Brazil. These findings reinforce the understanding of this rare glomerulopathy. ABSTRACT Aim Collapsing glomerulopathy (CG) is a glomerular disease that progresses rapidly to renal replacement therapy (RRT ...
Marcos Adriano Garcia Campos   +26 more
wiley   +1 more source

Koebner phenomenon in leukocytoclastic vasculitis: A case report and an updated review of the literature

open access: yesSAGE Open Medical Case Reports, 2019
Leukocytoclastic vasculitis is the most common form of cutaneous vasculitis. It is a neutrophilic small vessel vasculitis resulting from the deposition of circulating immune complexes.
Farah Kassam   +2 more
doaj   +1 more source

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