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

Haematologica. 2007 Mar;92(3):e34-6. doi: 10.3324/haematol.11057.

Authors

Yorick Sandberg¹, Ka L Wu, Freerk Heule, Renate R van den Bos, King H Lam, Anton W Langerak, Vincent H van der Velden, Kirsten van Lom, H Berna Beverloo

Affiliation

¹ Department of Immunology, Erasmus MC, University Medical Center Dr. Molewaterplein, 503015 GE Rotterdam, The Netherlands.

PMID: 17405754
DOI: 10.3324/haematol.11057

No abstract available

Publication types

Case Reports

MeSH terms

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*

Substances

Antigens, Neoplasm
Proto-Oncogene Proteins c-ets
Repressor Proteins