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

尖酸一點

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

glisten

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 .,