rev bras hematol hemoter. 2 0 1 7;3 9(2):167–169

Revista Brasileira de Hematologia e Hemoterapia Brazilian Journal of Hematology and Hemotherapy www.rbhh.org

Case Report

Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis – a very rare condition Sara Duarte a,b,∗ , Sónia Campelo Pereira a , Élio Rodrigues a , Amélia Pereira a a b

Internal Medicine Service, District Hospital of Figueira da Foz, EPE, Figueira da Foz, Portugal Clinical Hematology Department, University Hospital Center of Coimbra, Coimbra, Portugal

a r t i c l e

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Article history: Received 3 November 2016 Accepted 13 February 2017 Available online 11 March 2017

Introduction Chronic lymphocytic leukemia (CLL) is the commonest leukemia in adults. It is defined, according to the latest guidelines, as >5 × 103 /␮L circulating B lymphocytes (BL) expressing a typical cell surface marker signature (CD5+ , CD10− , CD19+ and CD20dim , surface immonuglobulindim , CD23+ , CD43+/− and cyclin D1− ).1 If lymph node enlargement and/or hepatosplenomegaly is present in a patient with

Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition.

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