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  2. Granulomatosis with polyangiitis - Wikipedia

    en.wikipedia.org/wiki/Granulomatosis_with...

    After a person with GPA has successfully undergone induction and gone into remission, the treatment goal then shifts to maintenance of remission and preventing subsequent GPA flares. Less toxic immunosuppressing medications such as rituximab, methotrexate, azathioprine, leflunomide, or mycophenolate mofetil are used. [27]

  3. Microscopic polyangiitis - Wikipedia

    en.wikipedia.org/wiki/Microscopic_polyangiitis

    The signs and symptoms of microscopic polyangiitis may resemble those of granulomatosis with polyangiitis (GPA) (another form of small-vessel vasculitis) but typically lacks the significant upper respiratory tract involvement (e.g., sinusitis) frequently seen in people affected by GPA. [citation needed]

  4. Systemic vasculitis - Wikipedia

    en.wikipedia.org/wiki/Systemic_vasculitis

    Necrotizing vasculitis, also called systemic necrotizing vasculitis, [1] is a general term for the inflammation of veins and arteries that develops into necrosis and narrows the vessels. [ 2 ] Tumors , medications, allergic reactions , and infectious organisms are some of the recognized triggers for these conditions, even though the precise ...

  5. 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.

  6. Eosinophilic granulomatosis with polyangiitis - Wikipedia

    en.wikipedia.org/wiki/Eosinophilic_granulomatos...

    Eosinophilic granulomatosis with polyangiitis consists of three stages, but not all patients develop all three stages or progress from one stage to the next in the same order; [7] whereas some patients may develop severe or life-threatening complications such as gastrointestinal involvement and heart disease, some patients are only mildly affected, e.g. with skin lesions and nasal polyps. [8]

  7. Polyarteritis nodosa - Wikipedia

    en.wikipedia.org/wiki/Polyarteritis_nodosa

    Small aneurysms are strung like the beads of a rosary, [4] therefore making this "rosary sign" an important diagnostic feature of the vasculitis. [5] PAN is sometimes associated with infection by the hepatitis B or hepatitis C virus. [6] The condition may be present in infants. [7] PAN is a rare disease. [6]

  8. 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.

  9. Avacopan - Wikipedia

    en.wikipedia.org/wiki/Avacopan

    Avacopan, sold under the brand name Tavneos, is a medication used to treat anti-neutrophil cytoplasmic autoantibody-associated vasculitis. [ 5 ] [ 6 ] [ 8 ] Avacopan is a complement 5a receptor antagonist [ 5 ] and a cytochrome P450 3A4 inhibitor.

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