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Severe Cytomegalovirus Reactivation in Patient with Low-Grade Non-Hodgkins Lymphoma after Standard Chemotherapy

机译:低度非霍奇金淋巴瘤标准化疗后严重的巨细胞病毒再激活

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摘要

Clinically significant cytomegalovirus (CMV) reactivation is not uncommon in patients with severe immunodeficiency secondary to underlying medical disorders or following aggressive immunosuppressive therapy. However, it is less frequently found in patients with low-grade haematological malignancies after nonintensive chemotherapy. We treated a patient at our centre for stage IVB follicular lymphoma with standard chemotherapy who successively developed CMV colitis associated with a CMV viral load of >3 million copies/ml. Four lines of antiviral treatment were necessary to obtain biochemical remission with undetectable CMV levels, with an initially insufficient response to valganciclovir despite therapeutic pre- and posttreatment levels. Subsequently, our patient also developed an infection with Pneumocystis jirovecii pneumonia (PJP) as further evidence of severe immune compromise. This case report demonstrates the importance of including investigations for less common sources of infection when confronted with a patient with a low-grade haematological malignancy and a pyrexia of unknown origin.
机译:具有临床意义的巨细胞病毒(CMV)重新激活在继发于基础医学疾病或积极免疫抑制治疗后患有严重免疫缺陷的患者中并不罕见。然而,在非强化化疗后低度血液恶性肿瘤患者中很少发现这种情况。我们用标准化学疗法治疗了IVB期滤泡性淋巴瘤分期中心的一名患者,该患者连续发展了CMV结肠炎,其CMV病毒载量大于300万拷贝/ ml。四线抗病毒治疗对于获得具有无法检测到的CMV水平的生化缓解是必需的,尽管治疗前和治疗后水平高,但最初对缬更昔洛韦的反应不足。随后,我们的患者还感染了吉氏肺孢子虫肺炎(PJP),这是严重免疫损害的进一步证据。该病例报告表明,对于血液病恶性程度低,来历不明的发热患者,应包括调查不常见的感染源的重要性。

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