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Acute hemorrhagic oedema of infancy, acute hemorrhagic edema of childhood, Finkelstein's disease, infantile postinfectious iris-like purpura and edema, medallion-like purpura, purpura en cocarde avec œdème and Seidlmayer syndrome. Purpura is one of the main characteristics of Acute hemorrhagic edema of infancy. Specialty: Dermatology: Symptoms
IgA vasculitis (HSP), previously known as Henoch–Schönlein purpura, is a disease of the skin, mucous membranes, and sometimes other organs that most commonly affects children. In the skin, the disease causes palpable purpura (small, raised areas of bleeding underneath the skin), often with joint pain and abdominal pain .
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 ...
Nonthrombocytopenic purpura is a type of purpura (red or purple skin discoloration) not associated with thrombocytopenia. [1] Nonthrombocytopenic purpura has been reported after smoking mentholated cigarettes. [2] Examples/causes include: Henoch–Schönlein purpura [3] Hereditary hemorrhagic telangiectasia [4] Congenital cytomegalovirus [1 ...
Henoch-Schönlein purpura (abdominal and joint pain associated with a purple rash that looks like bruises, often on the legs and buttocks) ... Multisystem inflammatory syndrome in children, aka ...
Henoch–Schönlein purpura (HSP) - Often considered a systemic form of IgA nephropathy, Henoch–Schönlein purpura (HSP) is a systemic small-vessel vasculitis that is characterized by deposition of IgA antibody immune complexes in different key areas throughout the body.
Thrombosis, transient ischemic attack, acute coronary syndrome, Budd-Chiari syndrome. [1] Causes: Overproduction of hematopoietic cells, genetic mutations. [1] Diagnostic method: Clinical criteria. Differential diagnosis: Chronic myelogenous leukemia, myelodysplastic syndrome, polycythemia vera, primary myelofibrosis, secondary thrombocytosis ...
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