Hagino Takeshi, Sato Tomohiko, Saga Reina, Hidai Hiroko, Murai Yoshiro, Akiyama Hideki, Motomura Sayuri
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.
Int J Hematol. 2022 Dec;116(6):961-965. doi: 10.1007/s12185-022-03422-9. Epub 2022 Jul 19.
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.
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。