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伪装成浸润性肾细胞癌的巨大肾嗜酸细胞瘤:病例报告及文献复习

Giant renal oncocytoma masquerading as infiltrating renal cell carcinoma: case report and literature review.

作者信息

Badmus T A, Adesunkanmi A R K, Agbakwuru C A, Salako A A, Uhunmwagho O, Eziyi A K

机构信息

Department of Surgery, Faculty of Clinical Sciences, College of Health Sciences, Obafemi Awolowo University, Ile-Ife Nigeria.

出版信息

Cent Afr J Med. 2006 Jan-Feb;52(1-2):16-9.

Abstract

Renal oncocytomas (RO) are tumours containing a population of cells with highly differentiated eosinophilic granular cytoplasm, extremely rich in mitochondria. It is estimated they account for about 3 to 7% of all solid renocortical tumours that were previously regarded as renal cell carcinoma. Based on their clinical behaviour and distinct pathologic features they are now regarded as benign renal tumours, often less than 5cm in diameter. We present a case of giant renal oncocytoma in a patient with synchronous bladder tumour, with pre-operative clinical, urographic and ultrasound features of locally advanced renal cell carcinoma (RCC). Findings at surgery included huge right renal tumour with infiltration to the duodenum; hepatic colic flexure; gall bladder; liver capsule and the greater omentum with small indurations at the base of the bladder. There was no tumour extension to the renal vein, no peritoneal seedling, no nodal metastasis and no ascites. Radical nephrectomy was carried out with good prognosis and without recurrence 52months post nephrectomy. This presentation, besides highlighting the possible giant nature of RO, also illustrates the malignant potential of RO to infiltrate contiguous structures and mimics infiltrating RCC. In view of the difficulties at establishing pre-operative diagnosis in this disease and because nephron-sparing surgery is curative, especially for the well-circumscribed tumours, RO should be considered in the management of patients with features of infiltrating RCC. A review of literature is also presented.

摘要

肾嗜酸细胞瘤(RO)是一种肿瘤,其细胞群体具有高度分化的嗜酸性颗粒细胞质,线粒体极其丰富。据估计,它们占所有实性肾皮质肿瘤的约3%至7%,这些肿瘤以前被视为肾细胞癌。基于其临床行为和独特的病理特征,它们现在被视为良性肾肿瘤,直径通常小于5厘米。我们报告一例患有同步膀胱肿瘤的巨大肾嗜酸细胞瘤患者,其术前临床、尿路造影和超声特征提示为局部晚期肾细胞癌(RCC)。手术所见包括巨大的右肾肿瘤,浸润至十二指肠、肝结肠曲、胆囊、肝包膜和大网膜,膀胱底部有小硬结。肿瘤未侵犯肾静脉,无腹膜种植,无淋巴结转移,无腹水。行根治性肾切除术,预后良好,肾切除术后52个月无复发。本病例除了突出RO可能具有的巨大性质外,还说明了RO浸润相邻结构并酷似浸润性RCC的恶性潜能。鉴于本病术前诊断困难,且保留肾单位手术具有治愈性,尤其是对于边界清楚的肿瘤,对于具有浸润性RCC特征的患者,在治疗时应考虑RO。本文还对文献进行了综述。

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