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一名患有血小板减少伴桡骨缺如综合征的成人急性髓系白血病。

Acute myelogenous leukemia in an adult with thrombocytopenia with absent radii syndrome.

作者信息

Go Ronald S, Johnston Kaye L

机构信息

Division of Internal Medicine, Gundersen Lutheran Medical Center, La Crosse, WI 54601, USA.

出版信息

Eur J Haematol. 2003 Apr;70(4):246-8. doi: 10.1034/j.1600-0609.2003.00054.x.

Abstract

Acute myelogenous leukemia with t(8;21)(q22;q22) developed in a 42-yr-old woman having thrombocytopenia with absent radii syndrome (TARS). Standard induction and postremission therapies were safely administered. With each successive chemotherapy, the onset of platelet recovery was not delayed, but peak platelet counts were persistently suppressed. Nine months after achieving complete hematologic and cytogenetic remission, she remains severely thrombocytopenic (platelet count 6-12 x 109/L). She is, however, asymptomatic and transfusion independent. Of interest is the transient normalization of platelet count (rebound relative thrombocytosis). Our report and review of the literature suggests that TARS, contrary to previous belief, may be associated with increased risk of acute leukemia.

摘要

一名患有血小板减少伴桡骨缺如综合征(TARS)的42岁女性发生了伴有t(8;21)(q22;q22)的急性髓系白血病。标准诱导缓解和缓解后治疗均安全实施。每次连续化疗时,血小板恢复的起始时间未延迟,但血小板峰值计数持续受到抑制。在实现完全血液学和细胞遗传学缓解9个月后,她仍严重血小板减少(血小板计数为6 - 12×10⁹/L)。然而,她没有症状且无需输血。值得关注的是血小板计数的短暂正常化(反弹性相对性血小板增多)。我们的报告及文献回顾表明,与之前的认知相反,TARS可能与急性白血病风险增加有关。

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