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  2. Myeloid sarcoma - Wikipedia

    en.wikipedia.org/wiki/Myeloid_sarcoma

    At least one case of FIP1L1-PDGFRA fusion gene-induced eosinophilic leukemia presenting with myeloid sarcoma and eosinophilia has been reported. This form of myeloid sarcoma is distinguished by its highly successful treatment with imatinib (the recommended treatment for FIP1L1-PDGRGA fusion gene-induced eosinophilic leukemia) rather than more aggressive and toxic therapy.

  3. Demyelinating disease - Wikipedia

    en.wikipedia.org/wiki/Demyelinating_disease

    Prognosis depends on the condition itself. Some conditions such as MS depend on the subtype of the disease and various attributes of the patient such as age, sex, initial symptoms, and the degree of disability the patient experiences. [14] Life expectancy in MS patients is 5 to 10 years lower than unaffected people. [15]

  4. Primary cutaneous acral CD8 positive T cell ...

    en.wikipedia.org/wiki/Primary_cutaneous_acral_CD...

    [2] [7] [20] The T-cells in these lesions do express T-cell receptor proteins, CD8 (a transmembrane glycoprotein that is a co-receptor for the T-cell receptor), TIA-1 (i.e., a granule-bound mRNA-binding protein), and in almost all cases (e.g., 26 of 28 cases in one study), the CD68 glycoprotein which is distributed in an unusual and distinctive ...

  5. CD68 - Wikipedia

    en.wikipedia.org/wiki/CD68

    CD68 immunostaining demonstrating macrophages and giant cells in a case of xanthogranulomatous pyelonephritis CD68 ( C luster of D ifferentiation 68) is a protein highly expressed by cells in the monocyte lineage (e.g., monocytic phagocytes , osteoclasts ), by circulating macrophages , and by tissue macrophages (e.g., Kupffer cells , microglia ).

  6. Erdheim–Chester disease - Wikipedia

    en.wikipedia.org/wiki/Erdheim–Chester_disease

    Erdheim–Chester disease (ECD) is an extremely rare disease characterized by the abnormal multiplication of a specific type of white blood cells called histiocytes, or tissue macrophages (technically, this disease is termed a non-Langerhans-cell histiocytosis).

  7. Mast cell activation syndrome - Wikipedia

    en.wikipedia.org/wiki/Mast_cell_activation_syndrome

    Mast cell activation syndrome (MCAS) is a term referring to one of two types of mast cell activation disorder (MCAD); the other type is idiopathic MCAD. [1] MCAS is an immunological condition in which mast cells, a type of white blood cell, inappropriately and excessively release chemical mediators, such as histamine, resulting in a range of chronic symptoms, sometimes including anaphylaxis or ...

  8. Ischemic fasciitis - Wikipedia

    en.wikipedia.org/wiki/Ischemic_fasciitis

    Immunohistochemistry analyses of IF tumors often show the presence of fibroblasts, fibroblast-like cells, and or other types of cells that in a percentage of cases express smooth muscle actin proteins, CD68 protein,. [6] desmin protein, [4] vimentin protein, and collagen type IV protein, but not keratin, S100, [6] calponin, or CD34 proteins. [1]

  9. Mast cell leukemia - Wikipedia

    en.wikipedia.org/wiki/Mast_cell_leukemia

    The leukemic cells usually are strongly positive for CD13, CD33, CD68, and CD117. Characteristically, basophil (e.g. CD11b, CD123) and monocyte markers (CD14, CD15) are absent. The cells usually express CD2 and CD25. [9] Malignant mast cells overexpress the anti-apoptosis gene, bcl-2. [10] A mutation called KIT mutation is detected in most ...

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