Suppr超能文献

儿童血液恶性肿瘤和干细胞移植受者的真菌感染。

Fungal infections in children with haematologic malignancies and stem cell transplant recipients.

机构信息

Division of Infectious Diseases, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Division of Oncology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

出版信息

Br J Haematol. 2020 May;189(4):607-624. doi: 10.1111/bjh.16452. Epub 2020 Mar 11.

Abstract

Children with haematologic malignancies and haematopoietic stem cell transplant recipients are at high risk for invasive fungal diseases (IFD). There has been an increased number of at-risk children over the past two decades due to improvements in cancer therapies resulting in improved survival of children with high-risk and refractory malignancies. The predominant organisms that cause IFD include Candida spp., Aspergillus spp. and the Mucorales molds. Clinical presentations of IFD vary based on host immune status and the causative organism. Though serum biomarkers such as the galactomannan assay and beta-D-glucan assay have been validated in adults, there are limited data regarding their diagnostic value in children. Thus, the gold standard for IFD diagnosis remains tissue biopsy with histopathological and microbiological evaluation. Treatment of IFD is multimodal and involves antifungal drugs, correction of immune dysfunction and surgical resection when feasible. Paediatric practice regarding IFD is largely extrapolated from data generated in adult patients; in this review, we evaluate both primary paediatric studies and guidelines intended for adult patients that are applied to paediatric patients. There remain significant knowledge gaps with respect to the prevention, diagnosis and treatment of IFD in immunocompromised children, and further research is needed to help guide management decisions.

摘要

患有血液系统恶性肿瘤和造血干细胞移植受者的儿童存在发生侵袭性真菌病(IFD)的高风险。由于癌症治疗的改进导致高危和难治性恶性肿瘤患儿的生存率提高,过去二十年中高危患儿的数量有所增加。引起 IFD 的主要病原体包括念珠菌属、曲霉菌属和毛霉目真菌。IFD 的临床表现取决于宿主免疫状态和病原体。尽管血清生物标志物,如甘露聚糖检测和β-D-葡聚糖检测已在成人中得到验证,但关于它们在儿童中的诊断价值的数据有限。因此,IFD 的诊断金标准仍然是组织活检,进行组织病理学和微生物学评估。IFD 的治疗是多模式的,涉及抗真菌药物、免疫功能障碍的纠正以及在可行时进行手术切除。儿科 IFD 的实践主要是从成人患者中获得的数据推断而来;在本综述中,我们评估了针对儿童患者应用的原发性儿科研究和针对成人患者的指南。在免疫功能低下的儿童中,IFD 的预防、诊断和治疗方面仍然存在重大知识空白,需要进一步研究以帮助指导管理决策。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验