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European LeukemiaNet study on the reproducibility of bone marrow features in masked polycythemia vera and differentiation from essential thrombocythemia.
Kvasnicka, Hans Michael; Orazi, Attilio; Thiele, Juergen; Barosi, Giovanni; Bueso-Ramos, Carlos E; Vannucchi, Alessandro M; Hasserjian, Robert P; Kiladjian, Jean-Jacques; Gianelli, Umberto; Silver, Richard; Mughal, Tariq I; Barbui, Tiziano.
Afiliación
  • Kvasnicka HM; Senckenberg Institute of Pathology, University of Frankfurt, Germany.
  • Orazi A; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.
  • Thiele J; Institute of Pathology, University of Cologne, Cologne, Germany.
  • Barosi G; Center for the Study of Myelofibrosis, Biotechnology Research Area, Istituto di Ricovero e Cura a Carattere Scientifico Policlinico S. Matteo Foundation, Pavia, Italy.
  • Bueso-Ramos CE; Department of Hematopathology, MD Anderson Cancer Center, Houston.
  • Vannucchi AM; Dipartimento di Medicina Sperimentale e Clinica, University of Florence, Florence, Italy.
  • Hasserjian RP; Department of Pathology, Massachusetts General Hospital, Boston.
  • Kiladjian JJ; Centre d'Investigations Cliniques, Hôpital Saint-Louis, Paris, France.
  • Gianelli U; Pathology Unit, University of Milan Medical School, Fondazione IRCCS Cà Granda, Ospedale, Italy.
  • Silver R; Weill Cornell Medical College, NewYork, NY.
  • Mughal TI; Tufts Medical Center, Boston.
  • Barbui T; Division of Hematology and Research Foundation, Ospedale Papa Giovanni XXIII, Bergamo, Italy.
Am J Hematol ; 92(10): 1062-1067, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28685840
The purpose of the study was to assess consensus and interobserver agreement among an international panel of six hematopathologists regarding characterization and reproducibility of bone marrow (BM) histologic features used to diagnose early stage myeloproliferative neoplasms, in particular differentiation of so-called masked/prodromal polycythemia vera (mPV) from JAK2-mutated essential thrombocythemia (ET). The six members of the hematopathology panel evaluated 98 BM specimens independently and in a blinded fashion without knowledge of clinical data. The specimens included 48 cases of mPV according to the originally published hemoglobin threshold values for this entity (male: 16.0-18.4 g/dL, female: 15.0-16.4 g/dL), 31 cases with overt PV according to the updated 2016 WHO criteria, and 19 control cases. The latter group included cases of JAK2-mutated ET, primary myelofibrosis, myelodysplastic syndrome, and various reactive conditions. Inter-rater agreement between the panelists was very high (overall agreement 92.6%, kappa 0.812), particularly with respect to separating mPV from ET. Virtually all cases of mPV were correctly classified as PV according to their BM morphology. In conclusion, a central blinded review of histology slides by six hematopathologists demonstrated that highly reproducible specific histological pattern characterize PV and confirmed the notion that there are no significant differences between mPV and overt PV in relation to BM morphology.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Policitemia Vera / Médula Ósea / Trombocitemia Esencial Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Hematol Año: 2017 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Policitemia Vera / Médula Ósea / Trombocitemia Esencial Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Hematol Año: 2017 Tipo del documento: Article País de afiliación: Alemania