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首页> 外文期刊>The American Journal of the Medical Sciences >Primary renal zygomycotic infarction mimicking renal neoplasia in an immunocompetent patient.
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Primary renal zygomycotic infarction mimicking renal neoplasia in an immunocompetent patient.

机译:免疫功能正常的患者,其原发性肾合霉菌性梗塞模仿了肾脏的肿瘤。

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摘要

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.
机译:极少有人用类真菌属的真菌生物体进行单独的肾脏感染,但是这些感染最常见于免疫功能低下的患者。我们报告了一个45岁的非洲裔美国人的情况,该人出现右侧肾盂肾炎的症状,包括发烧,排尿困难和胁腹疼痛。该患者的病史仅对镰状细胞性状有意义,未发现免疫抑制的证据。肾脏超声检查显示右肾上极低回声病变,影像学鉴别诊断包括肿瘤,脓肿和梗塞。尿液培养阴性,但尿液分析显示白细胞过多,无法计数。初次就诊后两周进行的腹部和骨盆的计算机断层扫描显示,尽管进行了抗微生物治疗,但肾脏的重量略有增加,随后进行了右肾切除术。大体切片时,在肾脏的上极发现了一个8.5厘米的界限清楚的病变。镜下切片显示肾实质广泛坏死,在梗死和存活的肾组织区域中,大,宽,呈虫状的真菌菌丝具有不规则的分支。在肾脏组织中发现血管浸润伴有血栓形成。该生物的形态特征与合子菌的形态特征最相容。在影像学研究中没有发现散播性真菌疾病的证据。该病例代表了在没有已知潜在的感染危险因素的患者中很少报道的孤立的肾脏合子菌病的成功结果,并说明了合子菌子菌感染可能的广泛临床表现。

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