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纯红细胞再生障碍伴 T 细胞大颗粒淋巴细胞白血病。

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

机构信息

Department of Hematology and Oncology, The Second Hospital of Jilin University.

Department of Anesthesia, China-Japan Union Hospital of Jilin University.

出版信息

J Biol Regul Homeost Agents. 2018 May-Jun;32(3):589-597.

PMID:29921385
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.

摘要

纯红细胞再生障碍性贫血 (PRCA) 是由于红系前体细胞在骨髓中无法成熟而导致的,最终导致贫血。我们在此报告一例 64 岁亚裔男性病例,四年前患有结直肠癌,接受了 6 个周期的奥沙利铂和卡培他滨治疗。该患者被诊断为 PRCA 和 T 细胞大颗粒淋巴细胞白血病。

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