PURE RED CELL APLASIA WITH T-CELL LARGE GRANULAR LYMPHOCYTIC LEUKEMIA

被引：2

作者：

Shi, G. ^{[1
]}

Hu, C-M. ^{[1
]}

Yu, Q. ^{[1
]}

Yang, N. ^{[1
]}

Xue, Z-S. ^{[1
]}

Zhao, B. ^{[1
]}

Guo, M. ^{[1
]}

Zheng, Y. ^{[2
]}

机构：

[1] Jilin Univ, Hosp 2, Dept Hematol & Oncol, Changchun, Jilin, Peoples R China

[2] Jilin Univ, China Japan Union Hosp, Dept Anesthesia, 126 Sendai St, Changchun 130033, Jilin, Peoples R China

来源：

JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS | 2018年 / 32卷 / 03期

关键词：

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

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：589 / 592

页数：4

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