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Titlebook: Cutaneous Lymphomas, Pseudolymphomas, and Related Disorders; Günter Burg,Otto Braun-Falco Book 1983 Springer-Verlag Berlin Heidelberg 1983

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Leukemic Lymphomas/LeukemiasIn this chapter, only series of “specific” skin infiltrates of some leukemias will be presented. Controversies and proposed leukemia classifications [42] will not be discussed. Lymphoid leukemias may be allied to the malignant lymphomas, since almost all lymphomas may give rise to a leukemic blood picture.
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Cutaneous PseudolymphomasObservations in a large series of skin lesions showing heavy lymphocytoid infiltrates comprises a heterogeneous group, both clinically and histopathologically:
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https://doi.org/10.1007/978-1-349-60671-9arities between them, lymphocytes are heterogeneous cells comprising two main groups; namely, B- (bursa of Fabricius, bone marrow-derived, fetal liver-derived) and T- (thymus-derived) lymphocytes, both of which have several subgroups [593, 652, 655]. B- and T-lymphocytes in man are thought to origin
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https://doi.org/10.1007/978-1-349-60671-9ing mononuclear phagocytic cells with strong lysosomal enzymatic activity from lymphocytes and in identifying distinct subpopulations of lymphoid cells. Lysozyme and α.-antichymotrypsin are highly characteristic, although not specific, markers of the monohistiocytic cell series and can be demonstrat
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https://doi.org/10.1007/978-1-137-10596-7r diffuse growth pattern, and that they may be composed of small and/or large cells. Various classifications have been proposed based upon these facts. The most commonly used is that suggested by Rappaport, whose system is simple, reproducible, and has been proven to be prognostically effective for
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History of the Middle Ages, 284-1500n (peak age, 4–8 years) of the so-called lymphoma belt of Central Africa. Sporadically cases in whites have been reported [513, 531, 587]. A possible causative agent is the Epstein-Barr virus, which, combined with a climate-dependent factor such as malaria, may induce the neoplasm.
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Introduction: History and Hints, of patients with Hodgkin’s disease. The most common nonspecific cutaneous manifestations are pruritus, prurigo-like lesions, and herpes zoster, which develop in at least about 15% of these patients [250]. In addition to these, many other lesions and conditions may be found [62, 666]: pallor, hyperp
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