The new WHO/EORTC classification for cutaneous lymphomas comprises mature T-cell and natural killer (NK)-Cell neoplasms, mature B-cell neoplasms, and immature hematopoietic malignancies. It reflects the unique features of lymphoproliferative diseases of the skin, and at the same time it is as compatible as possible with the concepts underlying the WHO classification for nodal lymphomas and the EORTC classification of cutaneous lymphomas. This article reviews the histological, phenotypical, and molecular genetic features of the various nosological entities included in this new classification. These findings always have to be interpreted in the context of the clinical features and biologic behavior. Aim: To review the histological, phenotypical and molecular genetic features of the various nosological entities of the new WHO/EORTC classification for cutaneous lymphomas. Methods: Extensive review of the literature cited in Medline and own data of the authors. Results: The WHO/EORTC classification of cutaneous lymphomas comprises mature T-cell and NK-cell neoplasms, mature B-cell neoplasms and immature hematopoietic malignancies. It reflects the unique features of primary cutaneous lymphoproliferative diseases. Conclusion: This classification is as much as possible compatible with the concept of the WHO classification for nodal lymphomas and the EORTC classification of cutaneous lymphomas. The histological, phenotypical and molecular genetic features always have to be interpreted in the context of the clinical features and biologic behavior.

WHO/EORTC classification of cutaneous lymphomas 2005: histological and molecular aspects / G. Burg, W. Kempf, A. Cozzio, J. Feit, R. Willemze, E.S. Jaffe, R. Dummer, E. Berti, L. Cerroni, S. Chimenti, J.L. Diaz-Perez, F. Grange, N.L. Harris, D.V. Kazakov, H. Kerl, M. Kurrer, R. Knobler, C.J..L..M. Meijer, N. Pimpinelli, E. Ralfkiaer, R. Russell-Jones, C. Sander, M. Santucci, W. Sterry, S.H. Swerdlow, M.H. Vermeer, J. Wechsler, S. Whittaker. - In: JOURNAL OF CUTANEOUS PATHOLOGY. - ISSN 0303-6987. - 32:10(2005), pp. 647-674.

WHO/EORTC classification of cutaneous lymphomas 2005: histological and molecular aspects

E. Berti;
2005

Abstract

The new WHO/EORTC classification for cutaneous lymphomas comprises mature T-cell and natural killer (NK)-Cell neoplasms, mature B-cell neoplasms, and immature hematopoietic malignancies. It reflects the unique features of lymphoproliferative diseases of the skin, and at the same time it is as compatible as possible with the concepts underlying the WHO classification for nodal lymphomas and the EORTC classification of cutaneous lymphomas. This article reviews the histological, phenotypical, and molecular genetic features of the various nosological entities included in this new classification. These findings always have to be interpreted in the context of the clinical features and biologic behavior. Aim: To review the histological, phenotypical and molecular genetic features of the various nosological entities of the new WHO/EORTC classification for cutaneous lymphomas. Methods: Extensive review of the literature cited in Medline and own data of the authors. Results: The WHO/EORTC classification of cutaneous lymphomas comprises mature T-cell and NK-cell neoplasms, mature B-cell neoplasms and immature hematopoietic malignancies. It reflects the unique features of primary cutaneous lymphoproliferative diseases. Conclusion: This classification is as much as possible compatible with the concept of the WHO classification for nodal lymphomas and the EORTC classification of cutaneous lymphomas. The histological, phenotypical and molecular genetic features always have to be interpreted in the context of the clinical features and biologic behavior.
T-cell lymphoma; granulomatous-slack-skin; woringer-kplopp-disease; of-the-literature; follicular myocosis-fungoides; BCL-2 protein expression; heavy-chain gene; Sezary-syndrome; intravascular lymphomatosis; pagetoid reticulosis
Settore MED/35 - Malattie Cutanee e Veneree
2005
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/436606
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