Gupta K L, Joshi K, Sud K, Kohli H S, Jha V, Radotra B D, Sakhuja V
Departments of Nephrology and Pathology, Postgraduate Institute of Medical Education, and Research, Chandigarh, India.
Nephrol Dial Transplant. 1999 Nov;14(11):2720-5. doi: 10.1093/ndt/14.11.2720.
Invasive zygomycosis (mucormycosis) occurs predominantly in immunocompromised patients in whom it carries a grave prognosis. While renal involvement is not so uncommon in disseminated infection, isolated renal zygomycosis is rare.
Forty-five patients with systemic zygomycosis were seen over a 12-year period from January 1986 to December 1997. Among these, 18 had renal involvement, nine with disseminated disease and nine with isolated renal zygomycosis. No underlying predisposing disease was identified in the majority of patients (72%). Renal involvement was confirmed at autopsy in 13 and by ante-mortem renal biopsy in five patients. The infection involved one kidney in five patients and was bilateral in the remaining. The manifestations included fever, flank pain, haematuria and pyuria with evidence of enlarged non-functioning kidneys on computerised tomography (CT). Of those with bilateral disease, 12 (92.3%) had anuric acute renal failure. Anti-fungal therapy was given to six patients (amphotericin B in mean total dose of 1.1 g) and of these only two with unilateral disease who also underwent nephrectomy survived while all the other 16 died.
This study shows that renal zygomycosis has emerged as a cause of acute renal failure in the last decade since no patient with renal involvement was identified at our centre prior to 1986 even though autopsies have been done regularly in patients dying of unknown causes. Bilateral renal zygomycosis should be suspected in any patient who presents with haematuria, flank pain and otherwise unexplained anuric renal failure. Characteristic CT findings and an early renal biopsy can confirm the diagnosis and help in effective management of this serious disease.
侵袭性接合菌病(毛霉菌病)主要发生于免疫功能低下的患者,预后严重。虽然在播散性感染中肾脏受累并不少见,但孤立性肾接合菌病却很罕见。
1986年1月至1997年12月期间共诊治了45例系统性接合菌病患者。其中,18例有肾脏受累,9例为播散性疾病,9例为孤立性肾接合菌病。大多数患者(72%)未发现潜在的易感疾病。13例患者经尸检证实肾脏受累,5例经生前肾活检证实。5例患者感染累及一侧肾脏,其余患者为双侧受累。临床表现包括发热、侧腹痛、血尿和脓尿,计算机断层扫描(CT)显示肾脏肿大且无功能。双侧患病的患者中,12例(92.3%)出现无尿性急性肾衰竭。6例患者接受了抗真菌治疗(两性霉素B平均总剂量为1.1g),其中仅2例单侧患病且接受了肾切除术的患者存活,其余16例均死亡。
本研究表明,肾接合菌病在过去十年中已成为急性肾衰竭的一个病因,因为尽管我们中心对死因不明的患者定期进行尸检,但在1986年之前未发现有肾脏受累的患者。对于任何出现血尿,侧腹痛及不明原因的无尿性肾衰竭的患者,均应怀疑双侧肾接合菌病。特征性的CT表现和早期肾活检可确诊该病,并有助于对这种严重疾病进行有效管理。