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骨髓增生异常综合征罕见地快速转化为急性白血病:一例报告

An Unlikely Rapid Transformation of Myelodysplastic Syndrome to Acute Leukemia: A Case Report.

作者信息

Pourmoussa Andrew, Kwan Karen

机构信息

Internist at the Los Angeles Medical Center in CA.

Physician in the Department of Hematology and Oncology at the Los Angeles Medical Center in CA.

出版信息

Perm J. 2017;21:16-091. doi: 10.7812/TPP/16-091.

Abstract

INTRODUCTION

Myelodysplastic syndrome is characterized by stem-cell-derived clonal myelopoiesis with an alteration in proliferation and differentiation. This condition carries a potential for transformation to acute leukemia, primarily in cases that are accompanied by high-risk features at diagnosis.

CASE PRESENTATION

A 68-year-old man with recently diagnosed myelodysplastic syndrome and Sweet syndrome (acute febrile neutrophilic dermatosis) presented to our Emergency Department with shortness of breath. During his hospital course, he developed signs and symptoms, predominantly consisting of respiratory difficulties, that were not typically characteristic of transformation to acute leukemia. Several days into his hospitalization, it was determined that the patient's underlying hematologic process seemed to have rapidly evolved into an acute myeloid leukemia, which accounted for the progression of symptoms. This patient ultimately opted for comfort measures only and died shortly thereafter.

DISCUSSION

Two important factors stood out as representing an atypical presentation. First, this patient lacked any of the high-risk features of myelodysplastic syndrome that typically portend transformation. In addition, his progression to acute leukemia in 28 days from the time of diagnosis was far more rapid than the 274-day median previously described in the literature. We theorize that the presence of Sweet syndrome may have served as a predisposing factor to transformation. This finding may offer benefit to physicians to potentially better predict this outcome and pursue more aggressive treatment measures earlier in the course of the disease in such a setting.

摘要

引言

骨髓增生异常综合征的特征是干细胞来源的克隆性骨髓造血,伴有增殖和分化改变。这种情况有转化为急性白血病的可能,主要发生在诊断时伴有高危特征的病例中。

病例介绍

一名68岁男性,近期诊断为骨髓增生异常综合征和Sweet综合征(急性发热性嗜中性皮病),因呼吸急促就诊于我们的急诊科。在他的住院过程中,出现了主要由呼吸困难组成的症状和体征,这些症状并非典型的急性白血病转化特征。住院几天后,确定患者潜在的血液学过程似乎迅速演变成了急性髓系白血病,这解释了症状的进展。该患者最终仅选择了舒适护理措施,此后不久死亡。

讨论

有两个重要因素代表了非典型表现。首先,该患者缺乏骨髓增生异常综合征中通常预示转化的任何高危特征。此外,他从诊断时起28天内进展为急性白血病,比文献中先前描述的274天中位数要快得多。我们推测Sweet综合征的存在可能是转化的一个易感因素。这一发现可能有助于医生在这种情况下更好地预测这一结果,并在疾病过程中更早地采取更积极的治疗措施。

相似文献

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[Transformation of myelodysplastic syndrome to acute lymphoblastic leukemia: 2 new cases].
An Pediatr (Barc). 2013 Jun;78(6):393-7. doi: 10.1016/j.anpedi.2012.10.003. Epub 2012 Nov 21.
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Childhood myelodysplastic syndromes in a Brazilian population.
Pediatr Hematol Oncol. 1999 Jul-Aug;16(4):347-53. doi: 10.1080/088800199277182.

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