Pathology and Genetics: Tumours of Haematopoietic and Lymphoid Tissues (World Health Organization Classification of Tumours) by Elaine Sarkin Jaffe
Pathology and Genetics: Tumours of Haematopoietic and Lymphoid Tissues (World Health Organization Classification of Tumours) Elaine Sarkin Jaffe ebook
ISBN: 9283224116, 9789283224112
The recent and ongoing rapid WHO Classification of Tumours of Haematopoietic and Lymphoid Tissue is the third volume in the new WHO series on histological and genetic typing of human tumors. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid tissues. In 1982 With the advancement of immunology and genetics, the characterization and algorithm of lymphomas have been taken over by the World Health Organization (WHO) Lymphoma Classification. New knowledge of disease molecular pathology, cytogenetic, epigenetic and genomic alterations have provided new strategies to attack and eradicate tumor cells at molecular level and significantly impacted our current therapeutics for hematological malignancies. Kyle, World Health Organization Classification Tumours of Haematopoietic and Lymphoid Tissues, IARC Press, Lyon, France, 2001. In the late 1970s and early 1980s the term “reticulum cell sarcoma” became a misnomer as researchers demonstrated the origin of the tumor cells to be transformed lymphoid cells (malignant B- and T- lymphocytes), not histiocytes. In: Jaffe E, Harris N, Stein H, Vardiman J, editors. Kleihues P, Sobin L (2001) Pathology and genetics of tumours of haematopoietic and lymphoid tissues. Case Reports in Pathology Volume 2012 (2012), Article ID 271407, 3 pages doi:10.1155/2012/271407. Primary brain tumours in adults. Among splenic lymphomas with circulating cells presenting cytoplasmic projections, a homogeneous clinico-pathological entity has been recently individualized as Splenic Diffuse Red Pulp Lymphomas (SDRPL) and introduced in the provisional. Comprehensive Geriatric Oncology.
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