Yadav Prakrati, Park Ji Yoon, Parisa Aijaz
Internal Medicine, Charleston Area Medical Center, Charleston, USA.
Cureus. 2025 Jan 28;17(1):e78131. doi: 10.7759/cureus.78131. eCollection 2025 Jan.
Xanthogranulomatous pyelonephritis (XGP) is a rare, chronic inflammatory renal disease typically caused by bacterial infections. We hereby report a rare case of bilateral XGP secondary to Candida albicans in a 31-year-old female with multiple autoimmune disorders. The patient presented with nonspecific abdominal discomfort, painful urination, and generalized weakness. Computed tomography (CT) of the abdomen revealed bilateral hydronephrosis, renal enlargement, and chronic changes consistent with XGP. Despite aggressive antifungal therapy, her renal function progressively deteriorated, ultimately leading to multi-organ failure and death. This case underscores the importance of maintaining a high index of suspicion for XGP in immunocompromised patients to facilitate early diagnosis and potentially improve outcomes. Additionally, it highlights the unique diagnostic challenge posed by C. albicans as a causative pathogen in XGP, emphasizing the need to consider fungal infections in the differential diagnosis to avoid delays in treatment.
黄色肉芽肿性肾盂肾炎(XGP)是一种罕见的慢性炎症性肾脏疾病,通常由细菌感染引起。我们在此报告一例31岁患有多种自身免疫性疾病的女性继发于白色念珠菌的双侧XGP罕见病例。患者表现为非特异性腹部不适、尿痛和全身无力。腹部计算机断层扫描(CT)显示双侧肾积水、肾脏肿大以及与XGP相符的慢性改变。尽管进行了积极的抗真菌治疗,但其肾功能仍逐渐恶化,最终导致多器官功能衰竭和死亡。该病例强调了在免疫功能低下患者中对XGP保持高度怀疑指数的重要性,以便于早期诊断并可能改善预后。此外,它突出了白色念珠菌作为XGP致病病原体所带来的独特诊断挑战,强调在鉴别诊断中需要考虑真菌感染以避免治疗延误。