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  2. Granulomatosis with polyangiitis - Wikipedia

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

    However, pulsed intravenous cyclophosphamide may be associated with a higher risk of GPA relapse when compared to oral cyclophosphamide. [8] Due to a high frequency of abnormally low white blood cell counts seen with cyclophosphamide treatment, Pneumocystis jirovecii pneumonia is a common complication, so prophylaxis against this pathogen is ...

  3. Cyclophosphamide - Wikipedia

    en.wikipedia.org/wiki/Cyclophosphamide

    Cyclophosphamide (CP), also known as cytophosphane among other names, [3] is a medication used as chemotherapy and to suppress the immune system. [4] As chemotherapy it is used to treat lymphoma , multiple myeloma , leukemia , ovarian cancer , breast cancer , small cell lung cancer , neuroblastoma , and sarcoma . [ 4 ]

  4. Henoch–Schönlein purpura - Wikipedia

    en.wikipedia.org/wiki/Henoch–Schönlein_purpura

    IgA vasculitis (HSP), previously known as Henoch–Schönlein purpura, is an autoimmune disease 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 .

  5. IgA nephropathy - Wikipedia

    en.wikipedia.org/wiki/IgA_nephropathy

    IgA nephropathy (IgAN), also known as Berger's disease (/ b ɛər ˈ ʒ eɪ /) (and variations), or synpharyngitic glomerulonephritis, is a disease of the kidney (or nephropathy) and the immune system; specifically it is a form of glomerulonephritis or an inflammation of the glomeruli of the kidney.

  6. ICD-10 - Wikipedia

    en.wikipedia.org/wiki/ICD-10

    ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]

  7. Vasculitis - Wikipedia

    en.wikipedia.org/wiki/Vasculitis

    The definite diagnosis of vasculitis is established after a biopsy of involved organ or tissue, such as skin, sinuses, lung, nerve, brain, and kidney. The biopsy elucidates the pattern of blood vessel inflammation. Some types of vasculitis display leukocytoclasis, which is vascular damage caused by nuclear debris from infiltrating neutrophils. [37]

  8. List of mental disorders in the DSM-IV and DSM-IV-TR ...

    en.wikipedia.org/wiki/List_of_mental_disorders...

    294.10: Dementia of the Alzheimer's Type, with late onset, without behavioral disturbance: Included only in the DSM-IV-TR. 301.6: Dependent personality disorder: 300.6: Depersonalization disorder: 311: Depressive disorder NOS: 315.4: Developmental coordination disorder: 799.9: Diagnosis deferred on Axis II: 799.9: Diagnosis or condition ...

  9. Pauci-immune - Wikipedia

    en.wikipedia.org/wiki/Pauci-immune

    In the setting of systemic vasculitis as described above, proliferative nephritis is associated with antineutrophil cytoplasmic antibodies (ANCA). [3] Because of this, an ANCA test should always follow a negative immunofluorescence result to have the highest accuracy for confirming pauci-immune vasculitis-driven proliferative nephritis.