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
Page: 352
ISBN: 9283224116, 9789283224112
Format: pdf
Publisher:

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. 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. As with virtually all WHO lymphoid neoplasms, the diagnosis of SMZL is based on elements of morphology (including peripheral blood villous lymphocytes when present), immunophenotype, and genetic information. In World Health Organization Classification of Tumors. Pathology and Genetics of Tumors of Haematopoietic and Lymphoid Tissues. Primary brain tumours in adults. Chan WC, Catovsky D, Foucar K, Monserrat E: T-cell large granular lymphocyte leukemia. Kyle, World Health Organization Classification Tumours of Haematopoietic and Lymphoid Tissues, IARC Press, Lyon, France, 2001. Lyon, France: International Agency for Splenic marginal-zone lymphoma: a distinct clinical and pathological entity. 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. Case Reports in Pathology Volume 2012 (2012), Article ID 271407, 3 pages doi:10.1155/2012/271407. The initial differential diagnosis WHO classification of tumours of hematopoietic and lymphoid tissues.