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As of 2017, the optimal way to treat Henoch–Schönlein purpura remains controversial. [22] Analgesics may be needed for the abdominal and joint pains. Wound care is warranted if skin death and ulcerations occur. [22] It is uncertain as to whether HSP needs treatment beyond controlling the symptoms.
Cryofibrinogenemia refers to a condition classified as a fibrinogen disorder in which a person's blood plasma is allowed to cool substantially (i.e. from its normal temperature of 37 °C to the near-freezing temperature of 4 °C), causing the (reversible) precipitation of a complex containing fibrinogen, fibrin, fibronectin, and, occasionally, small amounts of fibrin split products, albumin ...
Immune complex glomerulonephritis, as seen in Henoch-Schönlein purpura; this is an example of IgA involvement in a nephropathy. The reaction can take hours, days, or even weeks to develop, depending on whether or not there is immunological memory of the precipitating antigen. Typically, clinical features emerge a week following initial antigen ...
henoch schonlein purpura is a systemic vasculitis and the cause is vibrio cholerae. After Arcadian's request I'm working my way through this page. I hadn't watched it for some time. For some reason the reference on which I based my initial 2004 version (Saulsbury 2001) was deleted, but I'm gradually sourcing it back.
Purpura (/ ˈ p ɜːr p jʊər ə / [1]) is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure. The spots are caused by bleeding underneath the skin secondary to platelet disorders, vascular disorders, coagulation disorders, or other causes. [ 2 ]
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Inflammation-induced damage to the skin's blood vessels causes palpable purpura. Palpable purpura is the clinical manifestation of leukocytoclastic vasculitis, which can be idiopathic or linked to sepsis, reactions to drugs, connective tissue diseases, cryoglobulinemia, hepatitis C or B infection, or underlying cancers
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