Titlebook: Biopsy Pathology of the Lymphoreticular System; Dennis H. Wright,Peter G. Isaacson Book 1983 D. H. Wright and P. G. Isaacson 1983 biopsy.i

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Lymphadenopathy simulating malignant lymphoma,metimes pathologically. Similar conditions that have a recognized infective cause have been included in Chapter 2. Following previous custom (Butler, 1969; Dorfman and Warnke, 1974; Robb-Smith, 1947) we have divided these conditions into three groups according to the basic histologic pattern observe

Intersect

Aggrandize

Alveoli

Androgen

Malignant lymphomas derived from follicle centre cells and malignant lymphoma: immunoblastic,up of tumours is central to the histological diagnosis of malignant lymphoma. The cells that constitute the reactive follicle centre have been described and illustrated in Chapter 1 and reference to this normal cell population is of great help in the diagnosis of follicle centre cell lymphomas.

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esoteric

T-cell lymphomas,aggerated by under-recognition. Some neoplasms of T-lymphocytes have been reasonably well defined clinically and histologically. These are T-lymphoblastic lymphoma, a tumour of precursor T-cells that is dealt with in Chapter 10, chronic lymphocytic leukaemia of T-cell type and the cutaneous T-cell l

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Malignant lymphoma of B- and T-cell precursors,North America it is the commonest non-Hodgkin’s lymphoma of the paediatric age group. A high proportion of patients with lymphoblastic lymphoma, particularly in the younger age groups have, or subsequently develop, lymphoblastic leukaemia. The use of marker studies, specific antibodies and cytochemi

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Malignant lymphomas of the monocyte/macrophage system (histiocytic lymphomas),s previously designated as reticulum cell sarcomas, were termed histiocytic lymphomas in the Rappaport classification in the belief that they were derived from cells of the monocyte/macrophage system (Rappaport, 1966). Immunological and cytochemical marker studies (Table 11.1) have shown that the ma

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Miscellaneous,heterogeneous conditions in reported series of hairy cell leukaemia (Palutke ., 1981). The cells are characterized by the presence of cytoplasmic tartrate-resistant acid phosphatase and at the ultrastructural level by ribosomal lamellae, although these features are not entirely specific (Palutke .,