Department of Rheumatology, PD Hinduja National Hospital and Medical Research Centre, Veer Savarkar Marg, Mahim, Mumbai, Maharashtra, 400016, India.
Department of Rheumatology, PD Hinduja National Hospital and Medical Research Centre, Room No. 1107, Veer Savarkar Marg, Mahim, Mumbai, Maharashtra, 400016, India.
Clin Rheumatol. 2024 Feb;43(2):785-797. doi: 10.1007/s10067-023-06785-4. Epub 2023 Oct 6.
Patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV) are susceptible to opportunistic infections, including invasive fungal infections (IFI). This is due to many factors, including prolonged immunosuppressive therapy. The treatment of AAV with such IFIs is challenging.
A descriptive analysis of 5 patients with AAV complicated by concomitant invasive fungal infections was performed. We also have done a comprehensive literature review of IFIs in AAV using PubMed and Google Scholar databases.
All 5 patients initially received immunosuppressive medication but subsequently acquired IFI. One patient had sphenoid sinus involvement, and four had lung parenchymal involvement. Aspergillus infection was diagnosed in three patients, Cryptococcus infection in one patient and mixed infection with Aspergillus and Mucor infection in one patient. All our patients were on low doses of corticosteroids for several months to years or had received high-dose pulse steroids with cyclophosphamide in the last few weeks before being diagnosed with IFI. It was difficult to distinguish disease activity from IFI in all the cases. Two of the five patients died despite antifungal therapy. The literature review revealed a prevalence of IFIs ranging from 1 to 9.6% (excluding pneumocystis pneumonia). Aspergillosis was the predominant type of IFI, affecting 46 of 86 patients. Most of these patients (40/46) had pulmonary involvement. The prognosis for patients with IFI was consistently poor, as evidenced by 19 deaths out of 29 reported outcomes.
Overall, IFIs have a poor prognosis in patients with AAV. Differentiating disease activity from IFI is difficult because of similar organ distribution, imaging lesions, and histopathological characteristics. A high suspicion index and good-quality microbiology are needed for early treatment and prevention of mortality.
抗中性粒细胞胞质抗体相关性血管炎(AAV)患者易发生机会性感染,包括侵袭性真菌感染(IFI)。这是由于多种因素引起的,包括长期的免疫抑制治疗。治疗伴有此类 IFI 的 AAV 具有挑战性。
对 5 例 AAV 合并侵袭性真菌感染的患者进行描述性分析。我们还使用 PubMed 和 Google Scholar 数据库对 AAV 中的 IFI 进行了全面的文献回顾。
所有 5 例患者最初均接受免疫抑制治疗,但随后均发生 IFI。1 例患者累及蝶窦,4 例患者累及肺实质。3 例患者诊断为曲霉菌感染,1 例患者诊断为隐球菌感染,1 例患者为曲霉菌和毛霉菌混合感染。我们所有的患者均在数月至数年时间内接受低剂量皮质类固醇治疗,或在诊断 IFI 前的最后几周内接受高剂量脉冲类固醇联合环磷酰胺治疗。在所有病例中,均难以区分疾病活动与 IFI。尽管进行了抗真菌治疗,5 例患者中有 2 例死亡。文献回顾显示,IFI 的患病率为 1%至 9.6%(不包括肺孢子菌肺炎)。曲霉菌感染是 IFI 的主要类型,86 例患者中有 46 例。这些患者大多数(40/46)有肺部受累。IFI 患者的预后一直较差,29 例报告结局中有 19 例死亡。
总体而言,IFI 患者的预后较差。由于器官分布、影像学病变和组织病理学特征相似,因此难以区分疾病活动与 IFI。为了进行早期治疗和预防死亡,需要有较高的怀疑指数和高质量的微生物学检查。