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免疫功能正常患者中表现为肾肿瘤的原发性肾接合菌梗死。

Primary renal zygomycotic infarction mimicking renal neoplasia in an immunocompetent patient.

作者信息

Goel Suman, Carter James E, Culpepper Michael, Kahn Andrea G

机构信息

Departmens of Pathology, University of South Alabama Medical Center, Mobile, Alabama 36617, USA.

出版信息

Am J Med Sci. 2009 Oct;338(4):330-3. doi: 10.1097/MAJ.0b013e3181aa30d0.

DOI:10.1097/MAJ.0b013e3181aa30d0
PMID:19701078
Abstract

Isolated renal infections with fungal organisms of the class Zygomycetes are rare, but these infections are most frequently seen in patients who are immunocompromised. We report the case of a 45-year-old African American man who presented with symptoms of right-sided pyelonephritis, including fever, dysuria, and flank pain. The patient's history was significant only for sickle cell trait, and no evidence of immunosuppression was identified. Renal ultrasound imaging revealed a hypoechoic lesion in the superior pole of the right kidney, and the radiologic differential diagnoses included neoplasm, abscess, and infarct. Urine cultures were negative, but urinalysis showed white blood cells, which were too numerous to count. A computed tomography scan of the abdomen and pelvis performed 2 weeks after the initial presentation showed a slight increase in the renal mass, despite antimicrobial therapy, and a right nephrectomy was subsequently performed. On gross sectioning, an 8.5-cm well-circumscribed lesion was identified in the upper pole of the kidney. Microscopic sections showed extensive necrosis of the renal parenchyma, and, in areas of both infarcted and viable renal tissue, large, broad, aseptate fungal hyphae with irregular branching. Angioinvasion with associated thrombosis was seen in the renal tissue. The morphologic features of the organism were most compatible with that of a zygomycete. No evidence of disseminated fungal disease was identified on imaging studies. This case represents a successful outcome of a rarely reported isolated renal zygomycosis in a patient with no known underlying risk factors for the infection and illustrates the wide range of clinical presentations with which zygomycotic infections may present.

摘要

孤立性肾感染由接合菌纲真菌引起较为罕见,但这些感染最常见于免疫功能低下的患者。我们报告一例45岁非裔美国男性病例,该患者出现右侧肾盂肾炎症状,包括发热、排尿困难和侧腹痛。患者病史仅具有镰状细胞性状,未发现免疫抑制证据。肾脏超声成像显示右肾上极有一个低回声病变,影像学鉴别诊断包括肿瘤、脓肿和梗死。尿培养阴性,但尿液分析显示白细胞过多,无法计数。初次就诊2周后进行的腹部和盆腔计算机断层扫描显示,尽管进行了抗菌治疗,肾肿块仍略有增大,随后进行了右肾切除术。大体切片时,在肾上极发现一个8.5厘米边界清楚的病变。显微镜切片显示肾实质广泛坏死,在梗死和存活的肾组织区域均可见粗大、宽阔、无隔且有不规则分支的真菌菌丝。在肾组织中可见血管侵袭伴血栓形成。该生物体的形态学特征与接合菌最为相符。影像学检查未发现播散性真菌病证据。该病例代表了一例罕见的孤立性肾接合菌病在无已知潜在感染危险因素患者中的成功治疗结果,并说明了接合菌感染可能出现的广泛临床表现。

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