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孤立性肾毛霉菌病:病例报告与综述

Isolated renal mucormycosis: case report and review.

作者信息

Levy E, Bia M J

机构信息

Section of Nephrology, Yale University School of Medicine, New Haven, CT, USA.

出版信息

J Am Soc Nephrol. 1995 Jun;5(12):2014-9. doi: 10.1681/ASN.V5122014.

Abstract

The 15th reported case of isolated renal mucormycosis (infection of the kidney with fungus of the order Mucorales, in the absence of infection elsewhere in the body) is presented. The patient was a 36-year-old human immunodeficiency virus-infected man, actively using iv drugs, who suffered 6 wk of flank pain and fever before diagnosis was made by percutaneous renal biopsy. He received 4 months of amphotericin B treatment, then no therapy for 6 months before dying with no evidence of mucormycosis. Isolated renal mucormycosis should be suspected in those with an underlying immunocompromising illness or history of iv drug use who have persistent flank pain and fever, but sterile urine cultures. Computed tomographic scanning with contrast should then be performed; findings of severe inflammation or bacterial infection, despite an indolent clinical course with sterile or nondiagnostic urine and blood cultures, are suggestive of isolated renal mucormycosis, and renal biopsy under computed tomographic guidance should be performed, despite the potential risk of disseminated infection. Although our patient was treated with amphotericin B alone, nephrectomy with or without amphotericin B therapy appears to be more likely to cure infection and relieve pain and constitutional symptoms.

摘要

本文报告了第15例孤立性肾毛霉菌病(由毛霉目真菌感染肾脏,而身体其他部位无感染)病例。患者为一名36岁感染人类免疫缺陷病毒的男性,有静脉注射毒品史,在经皮肾活检确诊前,出现了6周的胁腹疼痛和发热症状。他接受了4个月的两性霉素B治疗,随后6个月未接受治疗,最终死亡,尸检未发现毛霉菌病迹象。对于有潜在免疫功能低下疾病或静脉注射毒品史、持续胁腹疼痛和发热但尿培养无菌的患者,应怀疑孤立性肾毛霉菌病。此时应进行增强计算机断层扫描;尽管临床病程进展缓慢、尿和血培养无菌或无诊断价值,但如果发现严重炎症或细菌感染,则提示孤立性肾毛霉菌病,尽管有播散性感染的潜在风险,仍应在计算机断层扫描引导下进行肾活检。虽然我们的患者仅接受了两性霉素B治疗,但肾切除术联合或不联合两性霉素B治疗似乎更有可能治愈感染,并缓解疼痛和全身症状。

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