由一种 Apophysomyces 菌引起的伊布替尼相关皮肤粘液瘤病:一例病例报告和文献综述。

IF 3.8 Q2 INFECTIOUS DISEASES Therapeutic Advances in Infectious Disease Pub Date : 2024-03-26 eCollection Date: 2024-01-01 DOI:10.1177/20499361241241199
Trung Minh Nguyen, Eva Amenta, Lynne Chapman, Sarvari Yellapragada, Bhuvaneswari Krishnan, Jonathan Lim, Richard J Hamill
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引用次数: 0

摘要

使用布鲁顿酪氨酸激酶抑制剂伊布替尼与侵袭性真菌感染(IFIs)有关。我们描述了一例与长期使用伊布替尼治疗慢性淋巴细胞白血病有关的 Apophysomyces 感染病例,并对使用伊布替尼的患者中的 Mucormycosis 感染进行了文献综述。我们的综述发现,IFI 可在开始使用酪氨酸激酶抑制剂的数月至数年内发病。这些报告更全面地说明了患者在服用伊布替尼期间发生 IFI 的风险。我们的病例还证明了分子技术在 IFI 诊断中的实用性,因为诊断是通过 28S rDNA/内部转录间隔聚合酶链式反应完成的。
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Ibrutinib-associated cutaneous mucormycosis due to an Apophysomyces species: report of a case and review of the literature.

The use of ibrutinib, a Bruton tyrosine kinase inhibitor, has been associated with invasive fungal infections (IFIs). We describe a case of Apophysomyces infection associated with long-term use of ibrutinib for the treatment of chronic lymphocytic leukemia as well as perform a literature review of Mucormycosis infections in patients on ibrutinib. Our review found that the onset of IFI can occur within months to years of starting tyrosine kinase inhibitors. These reports provide a more complete picture of the risk of IFI while patients are on ibrutinib. Our case also demonstrates the utility of molecular techniques in the diagnosis of IFI, as the diagnosis was made using 28S rDNA/internal transcribed spacer PCR.

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来源期刊
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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