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  2. Russell bodies - Wikipedia

    en.wikipedia.org/wiki/Russell_bodies

    Mott cells with Russell bodies (red arrows), compared to an almost normal plasma cell (white arrow; it has a prominent nucleolus). Plasmacytoma with abundant Russell bodies. H&E stain. Dutcher and Russell bodies. H&E stain. Russell bodies are inclusion bodies usually found in atypical plasma cells that become known as Mott cells. [1]

  3. Plasma cell - Wikipedia

    en.wikipedia.org/wiki/Plasma_cell

    Plasma cells with Dutcher and Russell bodies (H&E stain, 100×, oil) Plasma cells are large lymphocytes with abundant cytoplasm and a characteristic appearance on light microscopy . They have basophilic cytoplasm and an eccentric nucleus with heterochromatin in a characteristic cartwheel or clock face arrangement.

  4. Multiple myeloma - Wikipedia

    en.wikipedia.org/wiki/Multiple_myeloma

    The recent introduction of a commercial immunoassay for measurement of free light chains potentially offers an improvement in monitoring disease progression and response to treatment, particularly where the paraprotein is difficult to measure accurately by electrophoresis (for example in light chain myeloma, or where the paraprotein level is ...

  5. Biostatistics - Wikipedia

    en.wikipedia.org/wiki/Biostatistics

    As an example, consider groups of similar animals (mice, for example) under two different diet systems. The research question would be: what is the best diet? In this case, H 0 would be that there is no difference between the two diets in mice metabolism (H 0 : μ 1 = μ 2 ) and the alternative hypothesis would be that the diets have different ...

  6. Hypersegmented neutrophil - Wikipedia

    en.wikipedia.org/wiki/Hypersegmented_neutrophil

    Hypersegmentation can also be seen in many other conditions but with relatively less diagnostic significance. Hypersegmentation can sometimes be difficult to assert since interobserver variation is high and segmentation may vary with race.

  7. Pelger–Huët anomaly - Wikipedia

    en.wikipedia.org/wiki/Pelger–Huët_anomaly

    Is a benign dominantly inherited defect of terminal neutrophil differentiation as a result of mutations in the lamin B receptor gene. The characteristic leukocyte appearance was first reported in 1928 by Karel Pelger (1885-1931), a Dutch Hematologist, who described leukocytes with dumbbell-shaped bilobed nuclei, a reduced number of nuclear segments, and coarse clumping of the nuclear chromatin.

  8. Poikilocytosis - Wikipedia

    en.wikipedia.org/wiki/Poikilocytosis

    For example, poikilocytosis can be caused by a vitamin deficiency (e.g. vitamin B 12, folic acid), in which case the treatment is to replenish the deficient vitamin. It can be caused by a digestive disease, such as celiac disease , in which case the solution may lie in treating the underlying celiac disease so that nutrients can be properly ...

  9. Reactive lymphocyte - Wikipedia

    en.wikipedia.org/wiki/Reactive_lymphocyte

    Reactive lymphocytes were originally described by W. Türk in 1907 in the peripheral blood of patients with infectious mononucleosis.Later in 1923 the features of the reactive lymphocytes were characterized in greater detail by Hal Downey and C.A. McKinlay, who also discovered the association with EBV and CMV.