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Persistent thrombocytopenia post auto-SCT for AML treated with romiplostim in a patient with HIV.

机译:在接受HIV感染的患者中,接受romiplostim治疗的AML持续SCT后持续性血小板减少症。

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摘要

AML in the setting of HIV is rare. Delayed immune reconstitution remains a theoretical risk of treatment. We present a rare case in which auto-SCT was used for consolidation, complicated by autoimmune thrombocyto-penia managed by thrombopoietic growth factors.A 58-year-old man with HIV presented with pancyto-penia. BM biopsy confirmed AML with monoblastic morphology and trisomy 8 karyotype. Past history was significant for HIV diagnosed 10 years earlier, managed with antiretrovirals, etravirine 200 mg twice daily and the combination abacavir 300 mg/lamivudine 600 mg daily. At the time of AML diagnosis, HIV-1 RNA load was <40 copies/mL, with a CD4 count of 390 x 10~6/L and CD4/ CD8 ratio of 0.51. The patient also had a history of hepatitis C and had failed IFN and ribavirin treatment 5 years earlier, with a viral load of 1 x 10~7IU/mL at the time of AML diagnosis.
机译:在艾滋病毒感染者中,AML很少见。免疫重建延迟仍然是治疗的理论风险。我们提出了一种罕见的病例,其中使用auto-SCT进行巩固,并伴有由血小板生成因子控制的自身免疫性血小板减少症。一名58岁的HIV男性患者出现了全血细胞减少症。 BM活检证实AML具有单胚细胞形态和三体性8核型。过去的病史对于10年前诊断出的HIV具有重要意义,使用抗逆转录病毒药物,伊曲韦林200 mg每天两次和阿巴卡韦300 mg /拉米夫定600 mg每天联合治疗。在进行AML诊断时,HIV-1 RNA载量小于40拷贝/ mL,CD4计数为390 x 10〜6 / L,CD4 / CD8比率为0.51。该患者也有丙型肝炎病史,并且在5年之前未接受IFN和病毒唑治疗,在AML诊断时病毒载量为1 x 10〜7IU / mL。

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