肾移植后下肢潜伏肿块播散性贝氏坎宁哈默菌感染1例。

Yadi Wang, Keqin Zhang, Ling Liu, Runtian Qu
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引用次数: 0

摘要

背景:贝氏Cunninghamella bertholletiae (C. bertholletiae)是Mucorales目中一种罕见但毒性很强的物种,主要影响免疫系统受损的个体。由这种病原体引起的播散性感染经常导致严重的并发症,强调了及时诊断和积极治疗干预的必要性。侵袭性真菌病(IFDs)仍然是肾移植受者发病和死亡的主要原因,其特点是发病率和死亡率升高。真菌病原体的早期和精确鉴定对于优化患者预后至关重要。病例介绍:本报告报告了一个37岁男性肾移植受者的病例研究,他从潜在的下肢病变发展为弥散性柏氏梭菌感染。最初,他表现出高烧和呼吸困难的症状,导致诊断为败血症、严重肺炎、急性呼吸窘迫综合征和同种异体移植物功能障碍。术后复发胸腔积液,肺结节加重。新一代宏基因组测序(mNGS)证实了贝氏梭菌感染,组织病理学显示毛霉病伴血管侵犯、血栓形成和组织坏死。患者接受两性霉素B脂质复合物、泊沙康唑和异唑康唑13个月的抗真菌治疗。结论:该病例强调了组织病理学和mNGS在早期发现罕见IFDs中的重要作用,并强调了多学科方法结合手术和抗真菌治疗的必要性。使用三重抗真菌方案有效管理弥散性贝氏梭菌感染为未来病例提供了重要见解,强调了免疫功能低下患者早期诊断和个性化治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disseminated Cunninghamella bertholletiae Infection From Latent Lower Limb Mass After Kidney Transplant: A Case Report.

Background: Cunninghamella bertholletiae (C. bertholletiae), a rare yet highly virulent species within the Mucorales order, predominantly affects individuals with compromised immune systems. Disseminated infections caused by this pathogen frequently lead to severe complications, underscoring the necessity for prompt diagnosis and aggressive therapeutic interventions. Invasive fungal diseases (IFDs) continue to be a major cause of morbidity and mortality among kidney transplant recipients, characterized by elevated incidence and mortality rates. The early and precise identification of fungal pathogens is crucial for optimizing patient outcomes.

Case presentation: This report presents a case study of a 37-year-old male kidney transplant recipient who developed a disseminated C. bertholletiae infection from a latent lower limb lesion. Initially, he showed symptoms of high fever and dyspnea, leading to diagnoses of sepsis, severe pneumonia, acute respiratory distress syndrome, and allograft dysfunction. After surgery, he had recurrent pleural effusion and worsening pulmonary nodules. Metagenomic next-generation sequencing (mNGS) confirmed C. bertholletiae infection, and histopathology revealed mucormycosis with vascular invasion, thrombosis, and tissue necrosis. The patient underwent a 13-month antifungal treatment with amphotericin B lipid complex, posaconazole, and isavuconazole.

Conclusion: This case highlights the essential role of histopathology and mNGS in early detection of rare IFDs and stresses the need for a multidisciplinary approach combining surgery with antifungal therapy. The effective management of disseminated C. bertholletiae infection using a triple antifungal regimen offers important insights for future cases, underscoring the importance of early diagnosis and personalized treatment in immunocompromised patients.

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