Pure red cell aplasia with t-cell large granular lymphocytic leukemia

G. Shi, C-M. Hu, Q. Yu, N. Yang, Z-S. Xue, B. Zhao, M. Guo, Y. Zheng

Article ID: 5173
Vol 32, Issue 3, 2018
DOI: https://doi.org/10.54517/jbrha5173
Received: 9 July 2018; Accepted: 9 July 2018; Available online: 9 July 2018; Issue release: 9 July 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.


Keywords

pure red cell aplasia;T-cell large granular lymphocytic leukemia;chemotherapy;colorectal adenocarcinoma


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Supporting Agencies



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