Gao Xiaoning, Li Jie, Wang Lili, Lin Ji, Jin Hongshi, Xu Yihan, Wang Nan, Zhao Yu, Liu Daihong, Yu Li, Wang Quanshun
Department of Hematology, Chinese PLA General Hospital, Medical School of Chinese PLA, Beijing, China (mainland).
Department of Pathology, Chinese PLA General Hospital, Medical School of Chinese PLA, Beijing, China (mainland).
Am J Case Rep. 2016 Oct 27;17:793-798. doi: 10.12659/ajcr.899621.
BACKGROUND Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder characterized by the Philadelphia chromosome generated by the reciprocal translocation t(9: 22)(q34;q11). CML is usually diagnosed in the chronic phase. Blast crisis represents an advanced phase of CML. Extramedullary blast crisis as the initial presentation of CML with bone marrow remaining in chronic phase is an unusual event. Further, extramedullary blast crisis with T lymphoid/myeloid bilineal phenotype as an initial presentation for CML is extremely unusual. CASE REPORT Here, we report the case of a 49-year-old male with rapidly enlarged submandibular lymph nodes. Biopsy specimen from the nodes revealed a characteristic appearance with morphologically and immunohistochemically distinct myeloblasts and T lymphoblasts co-localized in 2 adjacent regions, accompanied by chronic phase of the disease in bone marrow. The presence of the BCR/ABL1 fusion gene within both cellular populations in this case confirmed the extramedullary disease represented a localized T lymphoid/myeloid bilineal blastic transformation of CML. After 3 courses of combined chemotherapy plus tyrosine kinase inhibitor treatment, the mass was completely regressed with a 3-log decrease in BCR/ABL1 transcript from baseline. Five months after the diagnosis, the patient showed diminished vision, hand tremors, and weakness of lower extremities. Flow cytometric immunophenotyping of cerebrospinal fluid revealed the presence of myeloid blasts. An isolated central nervous system relapse of leukemia was identified. Following high-dose systemic and intrathecal chemotherapy, the patient continued to do well. CONCLUSIONS The possibility of extramedullary blast crisis as an initial presentation in patients with CML should be considered. Further, an isolated central nervous system blast crisis should be considered if neurological symptoms evolve in patients who have shown a good response to therapy.
慢性髓系白血病(CML)是一种克隆性骨髓增殖性疾病,其特征是由相互易位t(9;22)(q34;q11)产生的费城染色体。CML通常在慢性期被诊断出来。急变期代表CML的晚期阶段。以髓外急变期作为CML的首发表现且骨髓仍处于慢性期是一种不寻常的情况。此外,以T淋巴/髓系双系表型的髓外急变期作为CML的首发表现极为罕见。病例报告:在此,我们报告一例49岁男性,其下颌下淋巴结迅速肿大。淋巴结活检标本显示出一种特征性表现,形态学和免疫组化上不同的髓母细胞和T淋巴母细胞共定位于两个相邻区域,同时骨髓处于疾病的慢性期。该病例中两个细胞群体均存在BCR/ABL1融合基因,证实髓外疾病代表CML的局限性T淋巴/髓系双系母细胞转化。经过3个疗程的联合化疗加酪氨酸激酶抑制剂治疗后,肿块完全消退,BCR/ABL1转录本较基线下降了3个对数。诊断后5个月,患者出现视力减退、手部震颤和下肢无力。脑脊液流式细胞免疫表型分析显示存在髓母细胞。确诊为孤立性中枢神经系统白血病复发。经过大剂量全身和鞘内化疗后,患者情况持续良好。结论:应考虑CML患者以髓外急变期作为首发表现的可能性。此外,如果对治疗反应良好的患者出现神经症状,应考虑孤立性中枢神经系统急变期。