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Atypical aleukemic presentation of large granular lymphocytic leukemia: a case report

机译:大颗粒性淋巴细胞白血病的非典型动脉瘤表现:一例报告

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摘要

Large granular lymphocytic leukemia (LGLL) is a rare lymphoproliferative disorder of transformed natural killer or T-cells attributed to chronic exposure to the proinflammatory cytokine IL-15. Diagnosis of the majority of T-cell LGLL is established by documenting clonal large granular lymphocytes (LGLs) in peripheral blood, by morphology and immunophenotype. The proteasome inhibitor bortezomib is known to target molecular pathways downstream of the IL-15 receptor signaling and has been proposed as a therapy in these patients. We report an uncommon presentation of LGLL with chronic neutropenia lacking typical blood LGLs, which failed to respond to bortezomib but obtained a very good partial remission with a classical methotrexate regimen.
机译:大颗粒淋巴细胞性白血病(LGLL)是一种罕见的转化性自然杀伤细胞或T细胞淋巴组织增生性疾病,可归因于长期暴露于促炎性细胞因子IL-15。大多数T细胞LGLL的诊断是通过形态和免疫表型记录外周血中的克隆性大颗粒淋巴细胞(LGL)来建立的。已知蛋白酶体抑制剂硼替佐米靶向IL-15受体信号传导下游的分子途径,并已被提议作为这些患者的疗法。我们报告了不常见的慢性中性粒细胞减少症,缺乏典型的血液LGLs的LGLL的表现,它对硼替佐米没有反应,但通过经典的氨甲蝶呤治疗获得了很好的部分缓解。

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