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  2. Chronic venous insufficiency - Wikipedia

    en.wikipedia.org/wiki/Chronic_venous_insufficiency

    Chronic venous insufficiency (CVI) is a medical condition characterized by blood pooling in the veins, leading to increased pressure and strain on the vein walls. [1] The most common cause of CVI is superficial venous reflux, which often results in the formation of varicose veins, a treatable condition. [2]

  3. Cutaneous small-vessel vasculitis - Wikipedia

    en.wikipedia.org/wiki/Cutaneous_small-vessel...

    If no underlying cause is found and the vasculitis is truly limited to the skin then treatment is primarily supportive. [13] Such treatment involves measures such as leg elevation, stockings, and topical steroids to relieve itching/burning. If the vasculitis does not self-resolve within 3–4 weeks, more aggressive treatment may be warranted. [13]

  4. Henoch–Schönlein purpura - Wikipedia

    en.wikipedia.org/wiki/Henoch–Schönlein_purpura

    Henoch–Schönlein purpura is a small-vessel vasculitis in which complexes of immunoglobulin A (IgA) and complement component 3 (C3) are deposited on arterioles, capillaries, and venules (hence it is a type III hypersensitivity reaction).

  5. Serum sickness - Wikipedia

    en.wikipedia.org/wiki/Serum_sickness

    The result is a leukocytoclastic vasculitis. [2] This results in hypocomplementemia, a low C3 level in serum. [2] They can also cause more reactions, causing the typical symptoms of serum sickness. This is similar to a generalised Arthus reaction. [2]

  6. Vasculitis - Wikipedia

    en.wikipedia.org/wiki/Vasculitis

    Vasculitis is a group of disorders that destroy blood vessels by inflammation. [2] Both arteries and veins are affected. Lymphangitis (inflammation of lymphatic vessels) is sometimes considered a type of vasculitis. [3] Vasculitis is primarily caused by leukocyte migration and resultant damage.

  7. Lupus vasculitis - Wikipedia

    en.wikipedia.org/wiki/Lupus_vasculitis

    Cutaneous vasculitis is the most common type of vasulitis amongst those with systemic lupus erythematosus. [7] The clinical presentation is variable and can include superficial ulcerations, splinter hemorrhages, panniculitis, macules, erythema with necrosis or erythematous plaques, cutaneous infarction, livedo reticularis, bullous lesions of the extremities or urticaria lesions, papulonodular ...

  8. Hereditary angioedema - Wikipedia

    en.wikipedia.org/wiki/Hereditary_angioedema

    Measuring C4 and C1-inhibitor levels. [2] Differential diagnosis: Intestinal obstruction, other types of angioedema [2] Prevention: C1 inhibitor [1] Treatment: Supportive care, medications [1] Medication: C1 inhibitor, ecallantide, icatibant [1] Prognosis: 25% risk of death if airway involved (without treatment) [2] Frequency ~1 in 50,000 [3]

  9. Cryoglobulinemic vasculitis - Wikipedia

    en.wikipedia.org/wiki/Cryoglobulinemic_vasculitis

    Cryoglobulinemic vasculitis is a form of inflammation affecting the blood vessels caused by the deposition of abnormal proteins called cryoglobulins. These immunoglobulin proteins are soluble at normal body temperatures, but become insoluble below 37 °C (98.6 °F) and subsequently may aggregate within smaller blood vessels.