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特发性难治性铁粒幼细胞贫血(IRSA)进展为急性混合性淋巴细胞 - 髓单核细胞白血病。病例报告及文献复习

Idiopathic refractory sideroachrestic anemia (IRSA) progressing to acute mixed lymphoblastic-myelomonoblastic leukemia. Case report and review of the literature.

作者信息

Hehlmann R, Zönnchen B, Thiel E, Walther B

出版信息

Blut. 1983 Jan;46(1):11-21. doi: 10.1007/BF00320001.

Abstract

A longitudinal observation of a patient with idiopathic refractory sideroachrestic anemia (IRSA) progressing to acute mixed lymphoblastic-myelomonoblastic leukemia is reported. The leukemia was characterized by morphology, immunological cell markers, and dissociated clinical responsiveness to vincristine/prednisone and arabinosylcytosine/6-thioguanine. Attention is paid to the hematological changes prior to leukemia development. Acute leukemia was best heralded in this patient by a severe deterioration of dyserythropoiesis and by an increase of blasts in the marrow to more than 5%. The observed preleukemic features are compared to those described in the literature.

摘要

报告了一例特发性难治性铁粒幼细胞贫血(IRSA)进展为急性混合淋巴细胞-髓单核细胞白血病患者的纵向观察结果。该白血病通过形态学、免疫细胞标志物以及对长春新碱/泼尼松和阿糖胞苷/6-硫鸟嘌呤的临床反应分离进行特征描述。重点关注白血病发生前的血液学变化。在该患者中,急性白血病的最佳预示是红细胞生成异常严重恶化以及骨髓中原始细胞增加至超过5%。将观察到的白血病前期特征与文献中描述的特征进行了比较。

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