Titlebook: Human Leukemias; Cytochemical and Ult Aaron Polliack Book 1984 Martinus Nijhoff Publishing, Boston 1984 cell.classification.leukemia.lympho

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ear-canal

The Ultrastructure of Monocytic Leukemiaincluded in the FAB classification [2] as M. (poorly differentiated or monoblastic) and M. (well differentiated or promonocytic). The existence of such a form was also recognized by Hayhoe [3]. who describes monocytic leukemia as the terminal phase of a spectrum starting from acute granulocytic leuk

seroma

Ultrastructural Observations in Therapy-Related Panmyelosistion of treatment of hematologic and nonhematologic malignancies and certain nonneoplastic disorders [1–9]. The incidence of acute leukemia in these patients is not well established but appears to be related to the intensity of therapy and age of the patient [10–12]. The interval from the commenceme

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Features of Therapy-Related Leukemia and their Comparison with Leukemia de Novo and with the Blast PCGL-BP). In this chapter we will discuss the morphologic, ultrastructural, and cytochemical characteristics of therapy-related or secondary myelodysplastic syndromes (2°-MDS) and ANLL (2°-ANLL), and we will compare these features with those of ANLL de novo and CGL-BP.

happiness

FECT

Acute Lymphoblastic Leukemiations’ World Health Organization (WHO) classification [1] and the French-American-British (FAB) classification based on Wright-Giemsa stained preparations of bone marrow smears [2, 3]. The FAB classification will be used throughout this chapter. This classification divides the lymphoblastic leukemia

PAGAN

Prolymphocytic Leukemia of B- and T-Cell Typesve splenomegaly and lymphocyte counts over 100 × 10./1, the diagnosis can be made only by identifying the prolymphocyte as the predominant cell in well-prepared peripheral blood films. The typical morphological features of the prolymphocyte—namely, larger size than a normal blood lymphocyte (or CLL)

contrast-medium

Ultrastructural Analysis of B- and T-Lymphocyte Subsets with the Immunogold Techniquelarly the development of monoclonal antibodies against antigens of hemopoietic cells, have proved to be of value in the characterization of normal and leukemic cells [1–3]. Several tracers such as immunoperoxidase, ferritin or colloidal gold particles [4] have been used at EM level to localize antig

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Admonish

Fine Structure of Leukemic T- and B-Cells, with Special Reference to Adult T-Cell Leukemia in Japanockets. B-cells generally contain more abundant rough endoplasmic reticulum (RER) than T-cells. On the other hand, pre-B-cells have as little RER as T-cells. Clustered dense granules, which exhibit lysosomal enzyme activities, seem to be a reliable ultrastructural marker of T-cells. Accumulation of