Sep 26, 2023 · Immunoglobulin A vasculitis (IgAV), formerly Henoch-Schönlein purpura, involves the small vessels of the joints, kidneys, gastrointestinal tract, and skin. IgAV can also affect the …

Henoch-Schönlein purpura is an acute, systemic, immune complex-mediated, leukocytoclastic vasculitis. It is characterized by a triad of palpable purpura (without thrombocytopenia), …

IgA vasculitis (HSP), previously known as Henoch–Schönlein purpura, is an autoimmune disease that most commonly affects children. In the skin, the disease causes palpable purpura (small, …

Abbreviation: HSP Classical triad of non-thrombocytopenic palpable purpura, abdominal pain, arthritis Most common vasculitis in childhood (usually 2-11 yr) More common in white/asian …

Feb 12, 2025 · a systemic immune-mediated small vessel vasculitis often following an upper respiratory infection and characterized by IgA deposition and triad of

Randomised, double-blind, placebo-controlled trial to determine whether steroids reduce the incidence and severity of nephropathy in Henoch-Schönlein Purpura (HSP).

Henoch-Schönlein Purpura (HSP) is a systemic vasculitis mediated by IgA and characterized by the clinical triad of non-thrombocytopenic palpable purpura, abdominal pain, and arthritis.

Jul 15, 2024 · What is the triad of Henoch-Schönlein purpura? The “triad” refers to three classic symptoms of HSP: red or purple bruises under the skin, belly pain, and joint pain.

Sep 21, 2021 · Henoch-Schonlein purpura is an inflammation of the small blood vessels of the skin, joints, bowels and kidneys. When blood vessels get inflamed, they can bleed into the …

Purpura not due to a low platelet count, caused by inflammation in blood vessels of the skin, is the hallmark of HSP. The tetrad of purpura, arthritis, kidney inflammation, and abdominal pain is …