Darling H S, Kumar Rajiv, Kapoor Rajan, Singh Jasjit, Verma Tarun
Department of Hematology, Army Hospital (R&R), Dhaula Kuan, New Delhi, 110010 India.
Indian J Hematol Blood Transfus. 2017 Dec;33(4):633-635. doi: 10.1007/s12288-017-0781-4.
Current hematology practice distinguishes chronic myeloid leukemia (CML) and other major chronic myeloproliferative neoplasms as different entities classically characterized by positivity of BCR-ABL fusion gene and JAK2V617F mutations. These are different in clinical presentation, molecular genetics, therapy and response to present treatments. Nevertheless, there have been occasional case reports of detection of both mutations in the same patient. Although some of these had been incidentally detected, most have manifested clinically while being treated for one disease. Here, we present two cases of co-existence of BCR-ABL and JAK2V617F positivity. The first one was initially managed as CML. On obtaining adequate molecular and hematological response, thrombocytosis persisted. Hence she was tested for JAK2V617F mutation. In the second case, when we noticed upfront very high platelet counts along with a clinical picture of CML, we tested her for both and was found to be positive for both. Till to date, no such clinical case has been reported from India. The current status and approach to BCR ABL and JAK2 coexistent mutations has been reviewed and discussed.
当前血液学实践将慢性髓系白血病(CML)和其他主要的慢性骨髓增殖性肿瘤视为不同的实体,其典型特征分别为BCR-ABL融合基因阳性和JAK2V617F突变阳性。这些疾病在临床表现、分子遗传学、治疗方法以及对现有治疗的反应方面均有所不同。然而,偶尔有病例报告称在同一患者中检测到这两种突变。尽管其中一些是偶然检测到的,但大多数是在治疗一种疾病时出现了临床症状。在此,我们报告两例BCR-ABL和JAK2V617F均呈阳性的病例。第一例最初被诊断为CML。在获得充分的分子学和血液学反应后,血小板增多症持续存在。因此,对她进行了JAK2V617F突变检测。在第二例中,当我们一开始就注意到血小板计数非常高且伴有CML的临床表现时,对她进行了这两种检测,结果发现均呈阳性。截至目前,印度尚未报告过此类临床病例。本文对BCR ABL和JAK2共存突变的现状及处理方法进行了综述和讨论。