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Cytoplasmic nucleophosmin is not detected in blastic plasmacytoid dendritic cell neoplasm
Authors:Fabio Facchetti  Stefano A Pileri  Claudio Agostinelli  Maria Paola Martelli  Marco Paulli  Adriano Venditti  Massimo F Martelli  and Brunangelo Falini
Institution:1Institute of Pathology, Spedali Civili, University of Brescia, Brescia;2Unit of Hematopathology, University of Bologna, Policlinico S. Orsola, Bologna;3Institute of Hematology, University of Perugia, Perugia;4Institute of Pathology, Policlinico “S. Matteo”, University of Pavia, Pavia and;5Institute of Hematology, University of Tor Vergata, Rome, Italy
Abstract:Acute myeloid leukemia carrying cytoplasmic mutated nucleophosmin (NPMc+ AML) and blastic plasmacytoid dendritic cell neoplasm have been included as new entities in the 4th edition (2008) WHO classification of myeloid neoplasms. These conditions may show clinical and pathological overlapping features (leukemic and skin involvement, and expression of macrophage markers). In this study, we provide evidence that aberrant cytoplasmic dislocation of nucleophosmin – the immunohistochemical surrogate for NPM1 mutations – allows the two entities to be genetically separated. In fact, nucleophosmin is consistently cytoplasmic in NPMc+ AML (because of the presence of NPM1 mutations), whilst it is nucleus-restricted (predictive of a germline NPM1 gene) in blastic plasmacytoid dendritic cell neoplasm. Our results clearly point cytoplasmic nucleophosmin (a full predictor of NPM1 mutations) as a new marker for distinguishing NPMc+ AML and blastic plasmacytoid dendritic cell neoplasm, further clarify the cell of origin of NPMc+ AML, and justify the inclusion of these pathological conditions as separate entities in the new WHO classification.
Keywords:plasmacytoid dendritic cells  acute myeloid leukemia  NPM1  nucleophosmin  mutations  antibodies  immunohistochemistry
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