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Successful rituximab treatment in a patient with refractory hairy cell leukemia-Japanese variant and suffering from acute respiratory distress

机译:利妥昔单抗成功治疗患有难治性毛细胞白血病-日本变异并患有急性呼吸窘迫的患者

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A 69-year-old man was referred to our hospital because of thrombocytopenia and was diagnosed as having hairy cell leukemia-Japanese variant (HCL-Jv) in December 2000. In June 2002, he was treated with pentostatin for progression of thrombocytopenia, but his response was incomplete. In addition, the number of hairy cells (HCs) in his peripheral blood (PB) began gradually to increase. He received treatment with interferon-alpha and cladribine, but he failed to respond completely to these treatments. The HCs in his PB decreased after splenic irradiation in July, 2004. However, he was admitted with acute respiratory distress in November. His white blood cell count was 123.1 X 10(9)/L with 91% HCs. Radiography and computed tomography of his chest revealed ground-glass opacity in both lungs. A bone marrow (BM) aspirate indicated increased cellularity with an 84% HC infiltration level. Based on these findings, we diagnosed pulmonary infiltration by HCs. Rituximab was administered weekly at a dose of 375 mg/m2, and he also received low-dose melphalan in a supportive role. After 8 courses of rituximab therapy, the HCs disappeared in his PB and BM, and his pulmonary infiltrates subsided. These results suggest that rituximab may be a very effective treatment for refractory HCL-Jv.
机译:一名69岁的男子因血小板减少症而被转诊到我院,并于2000年12月被诊断出患有日本毛状细胞白血病(HCL-Jv)。2002年6月,他接受喷喷他汀治疗血小板减少症,但是他的回答不完整。此外,其外周血(PB)中的毛细胞(HCs)数量开始逐渐增加。他接受了α-干扰素和克拉屈滨的治疗,但是他对这些治疗没有完全反应。 2004年7月接受脾脏照射后,PB中的HCs降低。但是,11月,他因急性呼吸窘迫而入院。他的白细胞计数为123.1 X 10(9)/ L,HCs为91%。 X光片和胸部X线计算机断层扫描显示两个肺部均出现毛玻璃样混浊。骨髓(BM)抽吸指示细胞增多,HC浸润水平为84%。基于这些发现,我们诊断出HCs导致肺部浸润。利妥昔单抗每周以375 mg / m2的剂量给药,他还接受了低剂量美法仑的支持作用。利妥昔单抗治疗8个疗程后,HCs在其PB和BM中消失,肺部浸润消退。这些结果表明,利妥昔单抗可能是治疗难治性HCL-Jv的非常有效的方法。

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