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Cystic nephroma: a case report and review of the literature

机译:囊性肾瘤:一例报告并文献复习

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Background The spectrum of cystic renal neoplasms includes both benign and malignant tumors and the order is as follows: benign multilocular cyst, multilocular cystic renal cell cancer and cystic renal cell cancer. Gross similarities among multicystic tumors of the kidney may cause conflict in the diagnosis and treatment of these lesions. Results We report a 53-year old male patient who presented with a mild persistent left flank pain and a painful left renal mass. After a series of examinations including abdominal ultrasound, intravenous pyelography and computed tomography, he underwent radical nephrectomy. Microscopic examination of the resected tissue showed the typical characteristics of a cystic nephroma. Immuno-histological staining of the epithelium of the tumour with CK 19 suggested an aberrant renal tubular differentiation. Conclusion Cystic nephroma is a relatively rare benign lesion of the kidney. Since 1892, only 200 cases have been reported in the international literature. The non-specific clinical findings and the poor contribution of imaging examinations make the preoperative distinction from other cystic renal neoplasias difficult. Final diagnosis can be established in the histopathological examination of the completely rejected tumor in the pathology laboratory.
机译:背景技术胆囊性肾肿瘤的频谱包括良性和恶性肿瘤,其顺序如下:良性多房性囊肿,多房性胆囊性肾细胞癌和胆囊性肾细胞癌。肾脏多囊性肿瘤之间的总体相似性可能会导致这些病变的诊断和治疗发生冲突。结果我们报告了一名53岁的男性患者,其表现为轻度持续性左胁腹疼痛和左肾肿痛。在进行了包括腹部超声,静脉肾盂造影和计算机断层扫描在内的一系列检查后,他接受了根治性肾切除术。切除组织的显微镜检查显示了囊性肾瘤的典型特征。 CK 19对肿瘤上皮的免疫组织学染色提示肾小管异常分化。结论囊性肾瘤是一种相对罕见的肾脏良性病变。自1892年以来,国际文献仅报道了200例。非特异性的临床发现和影像学检查的贡献不佳,使得术前难以与其他囊性肾瘤形成区分开。最终诊断可以在病理实验室对完全排斥的肿瘤进行组织病理学检查中确定。

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