Aplastic anemia with macrocytic anemia: a study based on long-term follow-up

To elucidate the clinical features, response rate, prognosis and clonal evolution of aplastic anemia (AA) with macrocytic anemia (mAA). The clinical features at initial diagnosis and data in follow up of mAA hospitalized from January 2000 to October 2011 were analyzed retrospectively. (1) Of 153/568...

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Veröffentlicht in:Zhōnghuá xuèyèxué zázhì 2013-02, Vol.34 (2), p.117-121
Hauptverfasser: Li, Ying-mei, Li, Xing-xin, Sun, Hui, Sun, Ling, Wan, Ding-ming, Liu, Lin-xiang, Chen, Sheng-mei, Chen, Shao-qian, Liu, Shao-jun, Zheng, Yi-zhou, Zou, Dian-bin
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Sprache:chi
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Zusammenfassung:To elucidate the clinical features, response rate, prognosis and clonal evolution of aplastic anemia (AA) with macrocytic anemia (mAA). The clinical features at initial diagnosis and data in follow up of mAA hospitalized from January 2000 to October 2011 were analyzed retrospectively. (1) Of 153/568 (26.9%) cases of mAA at initial diagnosis, 114(74.5%)were non-severe AA (NSAA), 39(25.5%)severe AA (SAA) and 0 very severe AA (VSAA), while the proportion was 16.2%, 45.2%, and 38.6% in 376 normocytic anemia AA (nAA), and the difference is statistically significant(χ(2) = 181.390; P = 0.000). The median age of mAA was significantly higher than that of nAA \[30(4 - 70)years vs 19 (3 - 68) years, P = 0.001\]. (2) There were no statistical difference in hemoglobin, absolute neutrophil count (ANC), platelet count (PLT), response rate after 6 months treatment and overall survival (OS) between mAA and nAA grouped in SAA and NSAA respectively. In SAA, the reticulocyte count (Ret) of mAA was significantly higher than that
ISSN:0253-2727