Results 1 to 10 of about 114,676,913 (192)

Immunoglobulin A Vasculitis Following COVID-19 Infection in an Adolescent Girl [PDF]

open access: yesOman Medical Journal
Immunoglobulin A vasculitis, formerly known as Henoch-Schoenlein purpura, is a rare acute auto-immune condition often associated with infections. We describe an adolescent girl who had recently recovered from COVID-19 infection.
Ahmed Atris   +3 more
doaj   +4 more sources

A Child with Immunoglobulin A Vasculitis and Hemorrhagic Shock: An Unusual Presentation

open access: yesAnnals of Rheumatology and Autoimmunity, 2021
Immunoglobulin A (IgA) vasculitis, formerly known as Henoch–Schonlein purpura, is the most common vasculitis in children affecting small-sized vessels. Although IgA vasculitis is a self-limiting disease, a small number of patients can present with severe
Shahad Alansari, Alhanouf Alsaleem
doaj   +2 more sources

COVID-19 associated immunoglobulin A vasculitis in an adult [PDF]

open access: yesJAAD Case Reports, 2022
Travis Vandergriff   +2 more
exaly   +4 more sources

A case and literature review of axial spondyloarthritis and immunoglobulin A vasculitis: Rare association or under-recognized? [PDF]

open access: yesSAGE Open Medical Case Reports
Axial spondyloarthritis (axSpA) is a chronic inflammatory arthritis affecting the spine and sacroiliac joints, often accompanied by extra-musculoskeletal manifestations involving the eyes, gut, and skin.
Robin Sia, Mueed Mian
doaj   +2 more sources

Recurrent diffuse alveolar hemorrhage in Immunoglobulin A vasculitis [PDF]

open access: yesRespiratory Medicine Case Reports
Introduction: Immunoglobulin A vasculitis (IgAV) is a small-vessel immune complex–mediated vasculitis that predominantly affects children, with significantly fewer cases reported in adults.
Joshua Woods, Baldeep Mann, Mehul Patel
doaj   +2 more sources

Immunoglobulin A vasculitis: The clinical features and pathophysiology [PDF]

open access: yesKaohsiung Journal of Medical Sciences
Palpable purpura, gastrointestinal symptoms, joint involvement, and renal disease characterize immunoglobulin A vasculitis (IgAV). Renal involvement ranging from mild proteinuria to severe nephritic or nephrotic syndrome highlights the importance of ...
Ya‐Chiao Hu   +2 more
doaj   +2 more sources

Gastrointestinal manifestations and pathogenesis in childhood immunoglobulin A vasculitis [PDF]

open access: yesFrontiers in Pediatrics
Immunoglobulin A vasculitis (IgAV), previously known as Henoch-Schönlein purpura, is the most common form of systemic vasculitis in childhood. The primary organs involved are the skin, gastrointestinal (GI) tract, joints, and kidneys.
Seiichi Kato   +2 more
doaj   +2 more sources

Adult-onset immunoglobulin A vasculitis

open access: yesAPIK Journal of Internal Medicine, 2021
We describe a case of adult-onset immunoglobulin A vasculitis (IgA vasculitis) presenting with cutaneous, renal and gastrointestinal manifestations without any evidence of articular involvement.
Megha Amarapur, Sangram Biradar
doaj   +1 more source

A clinical case of a complicated course of immunoglobulin A vasculitis with long-term nephritis: peculiarities of treatment

open access: yesZdorovʹe Rebenka, 2022
Immunoglobulin A vasculitis is the most common systemic vasculitis in children. Its course can be mild, involving only the skin and not requiring medical intervention, as well as severe, recurrent, long-lasting — when the gastrointestinal tract and ...
V.O. Synytska, O.R. Boyarchuk, O.I. Greh
doaj   +1 more source

Epidemiological and clinical aspects of immunoglobulin A vasculitis in childhood: a retrospective cohort study

open access: yesItalian Journal of Pediatrics, 2021
Background A retrospective study was conducted in order to investigate and describe the characteristics of Immunoglobulin A vasculitis (IgAV), previously known as Henoch-Schӧnlein purpura, in the paediatric population of a community-based healthcare ...
Breda Luciana   +7 more
doaj   +1 more source

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