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Clinically and genetically atypical T-cell prolymphocytic leukemia underlines the relevance of a multidisciplinary diagnostic approach

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Bibliographic Details
Published in:	Haematologica (Roma) 2007-03, Vol.92 (3), p.e34-e36
Main Authors:	Sandberg, Yorick, Wu, Ka L, Heule, Freerk, van den Bos, Renate R, Lam, King H, Langerak, Anton W, van der Velden, Vincent H, van Lom, Kirsten, Beverloo, H Berna
Format:	Article
Language:	English
Subjects:	Antigens, Neoplasm - analysis B-Lymphocytes - ultrastructure Biopsy Bone Marrow - pathology Chromosome Deletion Chromosomes, Human, Pair 12 - genetics Chromosomes, Human, Pair 12 - ultrastructure Chromosomes, Human, Pair 6 - genetics Chromosomes, Human, Pair 6 - ultrastructure Diagnostic Errors ETS Translocation Variant 6 Protein Humans Immunophenotyping In Situ Hybridization, Fluorescence Interdisciplinary Communication Leukemia, Prolymphocytic - diagnosis Leukemia, Prolymphocytic - genetics Leukemia, Prolymphocytic - pathology Lichen Nitidus - diagnosis Lymphoma, T-Cell, Cutaneous - diagnosis Lymphoma, T-Cell, Cutaneous - genetics Lymphoma, T-Cell, Cutaneous - pathology Male Middle Aged Proto-Oncogene Proteins c-ets - genetics Repressor Proteins - genetics Skin - pathology T-Lymphocytes - ultrastructure Translocation, Genetic
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