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急性早幼粒细胞白血病——15例患者的临床管理

Acute promyelocytic leukemia--clinical management of 15 patients.

作者信息

Daly P A, Schiffer C A, Wiernik P H

出版信息

Am J Hematol. 1980;8(4):347-59. doi: 10.1002/ajh.2830080403.

Abstract

Fifteen patients with acute promyelocytic leukemia (APL) were treated with anthracycline agents alone or combined with arabinosylcytosine (Ara C). Disseminated intravascular coagulation (DIC) was managed individually based on the presence of clinical as well as laboratory evidence of DIC. Ten patients received heparin. Eleven patients (73%) achieved complete remission (CR) but there were two early deaths from infection. The median duration of CR was 232 days (range, 41-780 days). Six patients were studied during ten relapses. In all cases, a morphologic picture more typical of acute myelocytic leukemia was seen during relapse but the DIC was similar in severity to that seen initially. Fever, without obvious infection and possibly due to the leukemic process, was a common presenting feature. Regenerating bone marrow aspirates in many patients who subsequently achieved CR without further treatment showed an inordinate number of promyelocytes, and this finding should not be immediately interpreted as disease resistant to therapy.

摘要

15例急性早幼粒细胞白血病(APL)患者接受了单独使用蒽环类药物或联合阿糖胞苷(Ara C)的治疗。根据弥散性血管内凝血(DIC)的临床及实验室证据,对DIC进行个体化处理。10例患者接受了肝素治疗。11例患者(73%)获得完全缓解(CR),但有2例因感染早期死亡。CR的中位持续时间为232天(范围41 - 780天)。对6例复发患者进行了研究。在所有病例中,复发时可见更典型的急性髓细胞白血病形态学表现,但DIC的严重程度与最初所见相似。发热是常见的临床表现,无明显感染,可能与白血病进程有关。许多随后未经进一步治疗即获得CR的患者,其骨髓穿刺再生时可见大量早幼粒细胞,这一发现不应立即解释为疾病对治疗耐药。

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