Jamil Syeda Firdos, Sharma Upendra, Singh Chaitali, Bansal Shashi
Department of Pathology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur, Rajasthan, India.
Department of Haemato-Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur, Rajasthan, India.
Indian J Pathol Microbiol. 2023 Jan-Mar;66(1):191-195. doi: 10.4103/ijpm.ijpm_441_21.
"Lineage switch" is term described when leukemic cells on relapse exhibit a new phenotype, where losses of one lineage defining markers with simultaneous gain of another lineage defining markers occur. Relapse of acute leukemia is although a very common event, lineage switch occurs and reported very rarely in such cases. The pathogenesis involved in this phenomenon remains unclear; however plasticity of hematopoietic progenitor affected by intrinsic and extrinsic environmental cues can be a possible explanation. In most of the cases at the time of relapse conversion of B-acute lymphoblastic leukemia (ALL) to acute myeloid leukemia (AML) occurs. Here, we presented an unusual case of 10 year old boy with AML switched to T-ALL upon relapse, which is very rare and not well documented till date in literature. The diagnosis was further supported by morphologic, cytochemistry and flowcytometric immunophenotyping (FCM-IPT). Prognosis and survival of such cases remains poor even by the use of standard chemotherapy.
“谱系转换”是一个术语,用于描述白血病细胞复发时呈现出新的表型,即一种谱系特异性标志物丢失,同时另一种谱系特异性标志物获得。急性白血病复发虽然是一个非常常见的事件,但谱系转换在这种情况下发生且报道极少。这种现象所涉及的发病机制仍不清楚;然而,受内在和外在环境因素影响的造血祖细胞的可塑性可能是一个解释。在大多数情况下,复发时会发生B急性淋巴细胞白血病(ALL)向急性髓系白血病(AML)的转化。在此,我们报告了一例不寻常的病例,一名10岁男孩患AML,复发时转变为T-ALL,这非常罕见,迄今为止文献中尚无充分记载。形态学、细胞化学和流式细胞免疫表型分析(FCM-IPT)进一步支持了诊断。即使使用标准化疗,此类病例的预后和生存率仍然很差。