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  2. Hypereosinophilic syndrome - Wikipedia

    en.wikipedia.org/wiki/Hypereosinophilic_syndrome

    Depending on eosinophil target-organ infiltration, the clinical presentation of hypereosinophilic syndrome (HES) varies from patient to patient. [13] Individuals with myeloproliferative variant HES may be more likely to experience mucosal ulcerations involving the genitalia or airways, while patients with lymphocytic variant HES typically exhibit prominent skin symptoms such as urticarial ...

  3. Eosinophilia - Wikipedia

    en.wikipedia.org/wiki/Eosinophilia

    An absolute eosinophil count is not generally needed if the CBC shows marked eosinophilia. [3] The location of the causal factor can be used to classify eosinophilia into two general types: extrinsic, in which the factor lies outside the eosinophil cell lineage; and intrinsic eosinophilia, which denotes etiologies within the eosinophil cell ...

  4. Chronic eosinophilic leukemia - Wikipedia

    en.wikipedia.org/wiki/Chronic_eosinophilic_leukemia

    Signs and symptoms may include weight loss, fever, malaise, cough, skin and mucosal lesions, diarrhea, and peripheral neuropathy. Cardiac symptoms are also possible. [2] In cases associated with PDGFRB and FGFR1 mutations, splenomegaly is common. Lymphadenopathy is also common with FGFR1 mutations. [2] Infiltration of eosinophils causes organ ...

  5. Eosinophilic gastroenteritis - Wikipedia

    en.wikipedia.org/wiki/Eosinophilic_gastroenteritis

    the presence of gastrointestinal symptoms, histological demonstration of eosinophilic infiltration in one or more areas of the gastrointestinal tract or presence of high eosinophil count in ascitic fluid (latter usually indicates subserosal variety), no evidence of parasitic or extraintestinal disease.

  6. Acute eosinophilic leukemia - Wikipedia

    en.wikipedia.org/wiki/Acute_eosinophilic_leukemia

    Patients with acute eosinophilic leukemia have a propensity for developing bronchospasm as well as symptoms of the acute coronary syndrome and/or heart failure due to eosinophilic myocarditis and eosinophil-based endomyocardial fibrosis. [1] [2] Hepatomegaly and splenomegaly are more common than in other variants of AML.

  7. Langerhans cell histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Langerhans_cell_histiocytosis

    The disease spectrum results from clonal accumulation and proliferation of cells resembling the epidermal dendritic cells called Langerhans cells, sometimes called dendritic cell histiocytosis. These cells in combination with lymphocytes , eosinophils , and normal histiocytes form typical LCH lesions that can be found in almost any organ . [ 5 ]

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