Abuzneid Yousef S, Alzeerelhouseini Hussam I A, Marzouqa Nizar, Yaghi Yasmine, Al-Ihribat Alaa R, Alqam Bilal, Krama Akram
Al-Quds University Faculty of Medicine, Jerusalem, Palestine.
Palestine Polytechnic University, Hebron, Palestine.
Ann Med Surg (Lond). 2021 Oct 30;71:102980. doi: 10.1016/j.amsu.2021.102980. eCollection 2021 Nov.
Atypical chronic myeloid leukemia ( is a rare myeloid neoplasm with poor prognosis and no current standard of treatment. It features both myelodysplastic and myeloproliferative characteristics with little data regarding mutations playing a role in the disease.
We present a case of a 55-year-old female complaining of fever, cough, general weakness and night sweats. Examinations showed leukocytosis with a left shift, thrombocytopenia, hypercellular bone marrow with marked granulocytic hyperplasia and a negative BCR-ABL. After ruling out myelodysplastic and other myeloproliferative diseases the patient was finally diagnosed as aCML according to the WHO criteria with mutations in the TET2 gene, the NRAS gene and in the KRAS gene. The patient was started on Hydroxyurea for a duration of 9 months with an excellent initial response leading to normalization of her platelets and WBCs. However, in the last month she stopped responding to therapy and her state of health started declining once again.
Atypical chronic myeloid leukemia ( with presence of TET2 gene mutation) is an unusual finding in myeloid neoplasms, have unknown prognosis and no current standard of treatment. It features both myelodysplastic and myeloproliferative characteristics with little data regarding mutations playing a role in the disease.
非典型慢性髓系白血病是一种罕见的髓系肿瘤,预后较差,目前尚无标准治疗方法。它兼具骨髓增生异常和骨髓增殖特征,关于在该疾病中起作用的突变的数据很少。
我们报告一例55岁女性,主诉发热、咳嗽、全身乏力和盗汗。检查显示白细胞增多伴左移、血小板减少、骨髓细胞增多伴明显粒细胞增生以及BCR-ABL阴性。在排除骨髓增生异常和其他骨髓增殖性疾病后,根据世界卫生组织标准,该患者最终被诊断为非典型慢性髓系白血病,伴有TET2基因、NRAS基因和KRAS基因的突变。患者开始使用羟基脲治疗9个月,初始反应良好,血小板和白细胞恢复正常。然而,在最后一个月,她对治疗不再有反应,健康状况再次开始下降。
(伴有TET2基因突变的)非典型慢性髓系白血病在髓系肿瘤中是一种不常见的发现,预后未知,目前尚无标准治疗方法。它兼具骨髓增生异常和骨髓增殖特征,关于在该疾病中起作用的突变的数据很少。