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肾囊肿的隐秘真相:一例肾囊肿内罕见的真菌侵袭性坏死性肉芽肿性炎症病例

Renal Cyst's Dark Secret: A Rare Case of Fungal-Infested Necrotizing Granulomatous Inflammation in a Renal Cyst.

作者信息

Jain R Punith, Aravind Suryaram, Gunabooshanam Barathi, Palaniyandi Velmurugan, Sekar Hariharasudhan, Krishnamoorthy Sriram

机构信息

Urology and Renal Transplantation, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

出版信息

Cureus. 2025 Jun 10;17(6):e85686. doi: 10.7759/cureus.85686. eCollection 2025 Jun.

Abstract

Fungal infections of renal cysts are exceptionally rare, particularly in immunocompetent individuals, and are often misdiagnosed due to nonspecific clinical and radiological findings. This report presents the first documented case of necrotizing granulomatous inflammation caused by Candida species within a renal cyst in an immunocompetent host. Here we present a 49-year-old immunocompetent male who presented with right loin pain and fever. He had a prior episode of renal cyst infection managed with percutaneous catheter drainage (PCD) three months earlier. Laboratory investigations revealed leukocytosis and marginally elevated serum creatinine. Imaging showed a thick-walled lower pole renal cyst (247 cc) with internal echoes, parenchymal thinning, and features suggestive of chronic obstruction. Initial management involved the use of empirical broad-spectrum antibiotics and ultrasound-guided aspiration with a 12 Fr pigtail catheter placement, yielding 180 mL of turbid fluid. Microbiological cultures, including bacterial and fungal, were negative. Due to persistent drainage and residual cavity on follow-up imaging, the patient underwent open cyst decortication with DJ stent removal. Histopathological analysis confirmed necrotizing granulomatous inflammation with fungal hyphae, consistent with Candida infection. Postoperatively, the patient was treated with oral fluconazole for six weeks. At two-month follow-up, he remained asymptomatic with no signs of recurrence. This case underscores the importance of considering fungal etiologies in persistent or recurrent renal cyst infections, even in immunocompetent patients. Histopathological confirmation is essential when cultures are inconclusive. Combined surgical and antifungal management remains key to achieving definitive resolution.

摘要

肾囊肿的真菌感染极为罕见,在免疫功能正常的个体中尤其如此,并且常因非特异性的临床和影像学表现而被误诊。本报告介绍了首例有文献记载的免疫功能正常宿主肾囊肿内由念珠菌属引起的坏死性肉芽肿性炎症病例。在此,我们报告一名49岁免疫功能正常的男性,他出现右腰疼痛和发热症状。三个月前他曾因肾囊肿感染接受经皮导管引流(PCD)治疗。实验室检查显示白细胞增多,血清肌酐略有升高。影像学检查显示一个厚壁的下极肾囊肿(247立方厘米),内部有回声,实质变薄,并有提示慢性梗阻的特征。初始治疗包括使用经验性广谱抗生素以及超声引导下穿刺抽吸并置入12F猪尾导管,抽出180毫升浑浊液体。包括细菌和真菌的微生物培养均为阴性。由于随访影像学检查发现持续引流和残留腔隙,患者接受了开放性囊肿剥脱术并取出DJ支架。组织病理学分析证实为伴有真菌菌丝的坏死性肉芽肿性炎症,符合念珠菌感染。术后,患者接受口服氟康唑治疗六周。在两个月的随访中,他无症状,无复发迹象。该病例强调了即使在免疫功能正常的患者中,对于持续性或复发性肾囊肿感染考虑真菌病因的重要性。当培养结果不明确时,组织病理学确认至关重要。手术和抗真菌联合治疗仍然是实现最终治愈的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb5b/12242881/834e8cf55497/cureus-0017-00000085686-i01.jpg

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