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Pure red cell aplasia with t-cell large granular lymphocytic leukemia
Vol 32, Issue 3, 2018
Abstract
Pure red cell aplasia (PRCA) develops as a result of erythroid precursors failing to reach maturity in the bone marrow, which eventually leads to anemia. Here we present a case of a 64-year-old Asian male with a medical history of colorectal adenocarcinoma who had been treated with 6 cycles of oxaliplatin and capecitabine four years ago. The patient was diagnosed with PRCA and T-cell large granular lymphocyte leukemia.
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Copyright (c) 2018 G. Shi, C-M. Hu, Q. Yu, N. Yang, Z-S. Xue, B. Zhao, M. Guo, Y. Zheng
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Medical Genetics, University of Torino Medical School, Italy

Department of Biomedical, Surgical and Dental Sciences, University of Milan, Italy