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慢性粒单核细胞白血病初次使用阿扎胞苷治疗后的髓样类白血病反应。

Myeloid leukemoid reaction after initial azacitidine therapy for chronic myelomonocytic leukemia.

作者信息

Hagino Takeshi, Sato Tomohiko, Saga Reina, Hidai Hiroko, Murai Yoshiro, Akiyama Hideki, Motomura Sayuri

机构信息

Department of Hematology, Tama-Hokubu Medical Center, Tokyo Metropolitan Health and Medical Treatment, Corporation 1-7-1 Aobachou, Higashimurayama-shi, Tokyo, 189-8511, Japan.

Division of Transfusion Medicine and Cell Therapy, The Jikei University Hospital, Tokyo, Japan.

出版信息

Int J Hematol. 2022 Dec;116(6):961-965. doi: 10.1007/s12185-022-03422-9. Epub 2022 Jul 19.

Abstract

The development of myeloid leukocytosis in leukemia patients during antileukemic treatment requires a differential diagnosis between myeloid leukemoid reaction and leukemia progression. We herein report the case of an 80-year-old Japanese man with chronic myelomonocytic leukemia (CMML) who developed marked myeloid leukocytosis (36.3 × 10/L) with 32.5% monocytes and 48% neutrophils about 4 weeks after the initial 5-azacitidine (AZA) treatment. The leukocytosis was unlikely to be attributed to infection and adverse drug reaction. As it resolved in a few days without any interventions, the transient myeloid leukocytosis was confirmed to be a myeloid leukemoid reaction. After four cycles of AZA treatment, leukemic blasts in the bone marrow decreased and the patient became transfusion-independent. Interestingly, levels of serum G-CSF showed a similar trend to the myeloid leukocytosis, while those of serum GM-CSF and IL-17 were undetectable throughout the clinical course, suggesting that a differentiation response to AZA treatment might lead to the myeloid leukemoid reaction. Our case implies that a marked but transient myeloid leukemoid reaction mimicking CMML progression can develop during AZA treatment, which requires careful clinical monitoring and differential diagnosis.

摘要

白血病患者在抗白血病治疗期间发生髓系白细胞增多症,需要对髓系类白血病反应和白血病进展进行鉴别诊断。我们在此报告一例80岁日本男性慢性粒单核细胞白血病(CMML)患者,在初始使用5-氮杂胞苷(AZA)治疗约4周后,出现显著的髓系白细胞增多症(36.3×10⁹/L),单核细胞占32.5%,中性粒细胞占48%。白细胞增多不太可能归因于感染和药物不良反应。由于在未进行任何干预的情况下,白细胞增多症在数天内消退,因此确诊短暂性髓系白细胞增多症为髓系类白血病反应。经过四个周期的AZA治疗后,骨髓中的白血病原始细胞减少,患者不再依赖输血。有趣的是,血清G-CSF水平与髓系白细胞增多症呈现相似趋势,而血清GM-CSF和IL-17水平在整个临床过程中均未检测到,这表明对AZA治疗的分化反应可能导致髓系类白血病反应。我们的病例提示,在AZA治疗期间可能会出现类似CMML进展的显著但短暂的髓系类白血病反应,这需要仔细的临床监测和鉴别诊断。

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