Barańska Marta, Kroll-Balcerzak Renata, Gil Lidia, Rupa-Matysek Joanna, Komarnicki Mieczysław
Department of Hematology and Bone Marrow Transplantation, Poznan University of Medical Sciences, Poznan, Poland.
Cent Eur J Immunol. 2017;42(1):111-115. doi: 10.5114/ceji.2016.65893. Epub 2017 May 8.
The number of patients with hematological malignancies who develop invasive fungal disease (IFD) has increased dramatically in recent decades. This increase is attributed to impairment of the host immune system due to intensive cytotoxic chemotherapies, use of corticosteroids and profound immunosuppression after hematopoietic stem cell transplantation (HSCT). Additionally, the increasing prevalence of fungal infections caused by emerging and rare pathogens, IFD of mixed etiology or of atypical localization is observed. There are also much more patients with IFD who do not belong to a well-described risk group, like patient with lymphoproliferative disorders. Within this heterogeneous group of patients, IFD epidemiology is not well defined and antifungal prophylaxis practices vary. The aim of this paper is to present the case of a 58-year-old patient with refractory Hodgkin disease, focusing on infectious complication after subsequent lines of chemotherapy. During deep and prolonged neutropaenia the patient developed symptoms of pneumonia. Despite antifungal prophylaxis with fluconazole, IFD of mixed etiology with the presence of Candida glabrata and Aspergillus fumigatus was diagnosed. The infection showed a poor response to monotherapy with liposomal amphotericin B, but was successfully treated with therapy involving micafungin. Analysis of the presented case demonstrated the necessity of new approaches to the prevention of IFD in patients with lymphoproliferative disorders heavily pretreated with numerous chemotherapy protocols. Prolonged neutropenia and high corticosteroid exposure put these patients in high risk of IFD like patients with acute myeloid leukemia/myelodysplastic syndrome or after allogeneic HSCT.
近几十年来,发生侵袭性真菌病(IFD)的血液系统恶性肿瘤患者数量急剧增加。这种增加归因于强化细胞毒性化疗、使用皮质类固醇以及造血干细胞移植(HSCT)后严重的免疫抑制导致宿主免疫系统受损。此外,还观察到由新出现的和罕见病原体引起的真菌感染患病率增加,以及病因混合或定位不典型的IFD。也有更多不属于明确风险组的IFD患者,如淋巴增殖性疾病患者。在这群异质性患者中,IFD的流行病学尚不明确,抗真菌预防措施也各不相同。本文旨在介绍一名58岁难治性霍奇金病患者的病例,重点关注后续化疗方案后的感染并发症。在深度和长期中性粒细胞减少期间,患者出现肺炎症状。尽管使用氟康唑进行了抗真菌预防,但仍诊断出由光滑念珠菌和烟曲霉引起的病因混合的IFD。该感染对脂质体两性霉素B单一疗法反应不佳,但使用米卡芬净治疗成功。对该病例的分析表明,对于接受过多种化疗方案大量预处理的淋巴增殖性疾病患者,需要采用新的方法来预防IFD。长期中性粒细胞减少和高剂量皮质类固醇暴露使这些患者像急性髓系白血病/骨髓增生异常综合征患者或异基因HSCT后患者一样,处于IFD的高风险中。