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伴 t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 和 KIT 外显子 8 突变的急性髓系白血病与特征性肥大细胞增多症和不良预后相关。

Acute myeloid leukemia with t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 and KIT Exon 8 mutation is associated with characteristic mastocytosis and dismal outcomes.

机构信息

Departments of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Departments of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

出版信息

Exp Mol Pathol. 2019 Jun;108:131-136. doi: 10.1016/j.yexmp.2019.04.009. Epub 2019 Apr 17.

Abstract

KIT mutations are observed in about 20-40% of acute myeloid leukemia with t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 [abbreviated AML t(8;21) here] with mutations involving exon 17 being the most common. Despite high frequencies of KIT mutations in both AML t(8;21) and systemic mastocytosis (SM), AML t(8;21) associated with SM is uncommon, and restricted to KIT exon 17 mutated cases. In this study, we report two cases of AML t(8;21) associated SM that KIT mutation occurred in exon 8 (T417_D419delinsY). In both patients, the bone marrow displayed increased round/ovoid mast cells with bilobated nuclei and absence of CD2 and CD25 expression. RUNX1/RUNX1T1 fusion was shown in both myeloblasts and mast cells by FISH. Patient #1 was refractory to induction chemotherapy and died at day 50; patient #2 had residual AML, marked SM, and persistent RUNX1/RUNX1T1 fusion after induction therapy.

摘要

KIT 突变在约 20-40%的伴有 t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 的急性髓系白血病(简称 AML t(8;21))中观察到,其中涉及外显子 17 的突变最为常见。尽管 AML t(8;21)和系统性肥大细胞增多症(SM)中 KIT 突变的频率较高,但与 SM 相关的 AML t(8;21)并不常见,仅限于 KIT 外显子 17 突变的病例。在这项研究中,我们报告了两例与 SM 相关的 AML t(8;21),KIT 突变发生在外显子 8(T417_D419delinsY)。在这两个患者中,骨髓中均显示出增多的圆形/卵圆形肥大细胞,具有双叶核,并且缺乏 CD2 和 CD25 的表达。FISH 显示在髓样母细胞和肥大细胞中均存在 RUNX1/RUNX1T1 融合。患者 #1 对诱导化疗有抵抗,在第 50 天死亡;患者 #2 在诱导治疗后仍有残留的 AML、明显的 SM 和持续的 RUNX1/RUNX1T1 融合。

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