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J Biol Regul Homeost Agents ; 32(3): 589-597, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29921385

RESUMO

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.


Assuntos
Leucemia Linfocítica Granular Grande/diagnóstico , Aplasia Pura de Série Vermelha/diagnóstico , Humanos , Masculino , Pessoa de Meia-Idade
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