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  2. Granulomatosis with polyangiitis - Wikipedia

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

    GPA treatment depends on the severity of the disease. [8] Severe disease is typically treated with a combination of immunosuppressive medications such as rituximab or cyclophosphamide and high-dose corticosteroids to control the symptoms of the disease and azathioprine , methotrexate , or rituximab to keep the disease under control.

  3. Palisaded neutrophilic and granulomatous dermatitis - Wikipedia

    en.wikipedia.org/wiki/Palisaded_neutrophilic_and...

    Palisaded neutrophilic and granulomatous dermaititis is associated with subacute bacterial endocarditis, [4] ledipasvir/sofosbuvir, [5] allopurinol, [6] Hodgkin’s and non-Hodgkin’s lymphoma, [4] chronic myelomonocytic leukemia, [7] ulcerative colitis, [8] Takayasu arteritis, [4] systemic vasculitis, [8] systemic lupus erythematosus (SLE), [9] sarcoidosis, [10] rheumatoid arthritis, [11 ...

  4. Eosinophilic granulomatosis with polyangiitis - Wikipedia

    en.wikipedia.org/wiki/Eosinophilic...

    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]

  5. Orofacial granulomatosis - Wikipedia

    en.wikipedia.org/wiki/Orofacial_granulomatosis

    Signs and symptoms may include: Persistent or recurrent enlargement of the lips, causing them to protrude. If recurrent, the interval during which the lips are enlarged may be weeks or months. The enlargement can cause midline fissuring of the lip ("median cheilitis") or angular cheilitis (sores at the corner of the mouth).

  6. Chronic granulomatous disease - Wikipedia

    en.wikipedia.org/wiki/Chronic_granulomatous_disease

    Chronic granulomatous disease (CGD), also known as Bridges–Good syndrome, chronic granulomatous disorder, and Quie syndrome, [1] is a diverse group of hereditary diseases in which certain cells of the immune system have difficulty forming the reactive oxygen compounds (most importantly the superoxide radical due to defective phagocyte NADPH oxidase) used to kill certain ingested pathogens. [2]

  7. Lymphomatoid granulomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphomatoid_granulomatosis

    Lymphomatoid granulomatosis (LYG or LG) is a very rare lymphoproliferative disorder first characterized in 1972. [1] Lymphomatoid means lymphoma -like and granulomatosis denotes the microscopic characteristic of the presence of granulomas with polymorphic lymphoid infiltrates and focal necrosis within it.

  8. COVID cases are rising. What are current guidelines ... - AOL

    www.aol.com/covids-still-rising-not-heres...

    Try to stay home and avoid seeing others until you notice no fever and your symptoms getting better for at least 24 hours. Following the 24 hours, you can go back to work, or school, and see your ...

  9. Granuloma inguinale - Wikipedia

    en.wikipedia.org/wiki/Granuloma_inguinale

    The disease often goes untreated because of the scarcity of medical treatment in the countries in which it is found. In addition, the painless genital ulcers can be mistaken for syphilis . [ 5 ] The ulcers ultimately progress to destruction of internal and external tissue, with extensive leakage of mucus and blood from the highly vascular lesions.