Abstract
T cell lymphomas are a heterogeneous group of neoplasms with variable clinical presentations, morphologic patterns, phenotypes and underlying genetic abnormalities. They are divided into precursor T cell (lymphoblastic) neoplasms of thymic origin and peripheral T-cell lymphomas (PTCL). According to the WHO classification, the latter comprise malignant tumors derived from post-thymic T cells and those derived natural killer (NK) cells. This heterogeneous group accounts for about 10–15 % of all lymphomas in most Western countries with a great geographic variation [1], being more prevalent in Asia at least partly reflecting the involvement of viruses in their pathogenesis such as human T lymphotrophic virus type 1 (HTLV-1) and Epstein–Barr virus (EBV). PTCLs are, with few exceptions, aggressive neoplasms with a poor response to therapy and a uniformly dismal prognosis [2].
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Gaulard, P., Hoeller, S. (2012). Misleading Features of Bone Marrow Involvement by Peripheral T-Cell Lymphomas. In: Anagnostou, D., Matutes, E. (eds) Bone Marrow Lymphoid Infiltrates. Springer, London. https://doi.org/10.1007/978-1-4471-4174-7_14
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DOI: https://doi.org/10.1007/978-1-4471-4174-7_14
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