Infectious Diseases Unit, Department of Medicine, University Hospital and University of Lausanne, CH-1011, Lausanne, Switzerland.
Parasitology-Mycology Laboratory, French National Reference Center for Echinococcosis, University Hospital of Besançon and Franche-Comté University, F-25030, Besançon, France - UMR 6249 CNRS-Franche-Comté University « Chrono-Environnement », F-25030, Besançon, France.
Parasite. 2023;30:9. doi: 10.1051/parasite/2023008. Epub 2023 Mar 31.
Alveolar echinococcosis (AE) is a severe parasitic infection caused by the ingestion of Echinococcus multilocularis eggs. While higher incidence and faster evolution have been reported in immunosuppressed patients, no studies have been performed specifically on AE in transplant patients. We searched for all de novo AE cases diagnosed between January 2008 and August 2018 in solid organ transplant (SOT) recipients included in the Swiss Transplant Cohort Study and the FrancEchino Registry. Eight cases were identified (kidney = 5, lung = 2, heart = 1, liver = 0), half of which were asymptomatic at diagnosis. AE diagnosis was difficult due to the low sensitivity (60%) of the standard screening serology (Em2+) and the frequently atypical radiological presentations. Conversely, Echinococcus Western blot retained good diagnostic performances and was positive in all eight cases. Five patients underwent surgery, but complete resection could only be achieved in one case. Moreover, two patients died of peri-operative complications. Albendazole was initiated in seven patients and was well tolerated. Overall, AE regressed in one, stabilized in three, and progressed in one case, and had an overall mortality of 37.5% (3/8 patients). Our data suggest that AE has a higher mortality and a faster clinical course in SOT recipients; they also suggest that the parasitic disease might be due to the reactivation of latent microscopic liver lesions through immune suppression. Western blot serology should be preferred in this population. Finally, surgery should be considered with caution, because of its low success rate and high mortality, and conservative treatment with albendazole is well tolerated.
泡型包虫病 (AE) 是一种严重的寄生虫感染,由摄入细粒棘球绦虫的虫卵引起。虽然在免疫抑制患者中报告的发病率更高且进展更快,但尚未针对移植患者进行专门的 AE 研究。我们在瑞士移植队列研究和 FrancEchino 注册中心中搜索了所有在 2008 年 1 月至 2018 年 8 月期间诊断为新发病例的实体器官移植 (SOT) 受者中的 AE 病例。确定了 8 例(肾=5 例,肺=2 例,心=1 例,肝=0),其中一半在诊断时无症状。由于标准筛查血清学 (Em2+) 的敏感性低(60%)和经常出现非典型放射学表现,AE 诊断困难。相反,Echinococcus Western blot 保留了良好的诊断性能,在所有 8 例中均为阳性。5 例患者接受了手术,但仅在 1 例中实现了完全切除。此外,2 例患者死于围手术期并发症。7 例患者开始使用阿苯达唑,且耐受性良好。总体而言,AE 在 1 例中消退,3 例稳定,1 例进展,总死亡率为 37.5%(8 例患者中的 3 例)。我们的数据表明,AE 在 SOT 受者中具有更高的死亡率和更快的临床病程;它们还表明寄生虫病可能是由于免疫抑制导致潜伏的微小肝病变重新激活。在该人群中,Western blot 血清学应作为首选。最后,由于手术成功率低且死亡率高,因此应谨慎考虑手术,并且阿苯达唑的保守治疗具有良好的耐受性。