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EBV post transplantation lymphoproliferative disease-associated pneumomediastinum in a pediatric patient with long-lasting low loads of plasma EBV-DNA positivity

机译:长期持续低负荷血浆EBV-DNA阳性的小儿患者EBV移植后与淋巴增生性疾病相关的肺炎纵隔

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We report a patient with extensive chronic-GVHD (c-GVHD) after BMT in whom pneumomediastinum and subcutaneous emphysema developed as the first sign of EBV post transplantation lymphoproliferative disease (PTLD) after long-lasting low loads of plasma EBV-DNA positivity.A 3-year-old boy in second CR for T-cell leukemia received BMT from an HLA-A allele-mismatched unrelated donor. The course was complicated by extensive c-GVHD disease of the skin and gastrointestinal tract, for which he was treated with CsA and prednisolone. Four months after BMT, he was admitted because of neutropenic fever. Shortly thereafter, he developed dyspnea, tachypnea and oxygen dependency. A chest X-ray revealed pneumomediastinum (Figure 1, arrow heads) with subcutaneous emphysema (Figure 1, black arrows) and prominent mediastinal masses (Figure 1, white arrow), suspected to be lymphomas. The weekly monitoring for EBV by PCR in plasma had been positive for 8 weeks. It showed relatively low loads ranging from 50 to 3600 copies/mlwithout any symptoms. In the weeks before theevent, loads spontaneously decreased to 100-300 copies/ml, and at the time of the event, the plasma viral load was 265 copies/ml.
机译:我们报告了一名BMT后患有广泛性慢性GVHD(c-GVHD)的患者,在长期低血浆血浆EBV-DNA阳性后,肺炎纵隔和皮下气肿发展成为EBV移植后淋巴增生性疾病(PTLD)的第一个迹象。 T细胞白血病第二次CR的3岁男孩从HLA-A等位基因不匹配的无关供者接受BMT。该过程因皮肤和胃肠道广泛的c-GVHD疾病而变得复杂,为此他接受了CsA和泼尼松龙的治疗。 BMT后四个月,他因中性粒细胞减少症而入院。此后不久,他出现呼吸困难,呼吸急促和氧气依赖。胸部X线检查显示肺炎性纵隔(图1,箭头)和皮下气肿(图1,黑色箭头)和明显的纵隔肿物(图1,白色箭头),怀疑是淋巴瘤。每周用血浆PCR监测EBV阳性8周。它显示出相对较低的负载,范围从50到3600拷贝/毫升,没有任何症状。在事件发生前的几周内,载量自发降至100-300拷贝/毫升,在事件发生时,血浆病毒载量为265拷贝/毫升。

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