Results 61 to 70 of about 9,671 (180)

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

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

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  

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

Primary Systemic Vasculitis in Childhood [PDF]

open access: yes, 2012
As vasculites sistémicas constituem um grupo de doenças, pouco frequentes na infância, caracterizadas por inflamação e necrose vascular. A sua tradução clínica é heterogénea, condicionada pelo tipo de vaso e orgão afectados. Recentemente foi proposta uma
Amaro, C, Pereira, N
core  

"Etude rétrospective des cas de vasculite cutanée identifiés au laboratoire de dermopathologie du CHUV de 2006 à 2010" [PDF]

open access: yes, 2012
CONTEXTE Les vasculites représentent un groupe de maladies inflammatoires touchant tous les vaisseaux, des grosses artères aux artères de plus petit calibre, en passant par les capillaires et les veines, de toutes tailles également.
Joris, F.
core  

A High Estimated Prevalence of Onychomycosis Exists Among Danish Children

open access: yesMycoses, Volume 68, Issue 11, November 2025.
ABSTRACT Background The prevalence of onychomycosis among children is suspected to be increasing. The current global prevalence of paediatric onychomycosis ranges from 0% to 7.7%. Clinical observations in Denmark suggest the same but to our knowledge no study exists estimating the prevalence of onychomycosis among Danish children.
Tanja Roehmer Wriedt   +6 more
wiley   +1 more source

Henoch-Schönlein Purpura: A Literature Review

open access: yesActa Dermato-Venereologica, 2017
Henoch-Schönlein purpura is the most common childhood vasculitis, but may also affect adults. This article reviews the literature since 2011 on advances in diagnosis, clinical disease manifestations, pathophysiology and treatment of Henoch-Schönlein ...
Liv Eline Hetland   +3 more
doaj   +1 more source

JAK Inhibitors for Treatment of SAPHO Syndrome: A Systematic Review of 72 Cases

open access: yesACR Open Rheumatology, Volume 7, Issue 10, October 2025.
Objective Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome usually involves bones, joints, and skin. Due to a lack of known pathogenesis and clinical trials, there is no standard treatment of SAPHO syndrome. Because none of the current treatments have a high efficacy and the risk of relapse is high, new treatment options for ...
Patrick Fazeli   +9 more
wiley   +1 more source

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