Han Xi-nian, Peng Ling-rong, Liu Guang-hua, Wang Jian
Department of Diagnostic Radiology, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China.
Zhonghua Zhong Liu Za Zhi. 2007 May;29(5):382-5.
To investigate the role of multiphasic spiral computed tomography (SCT) in the differential diagnosis of small renal cell carcinoma.
The data of 100 patients with small renal cell carcinoma (< or = 3.0 cm) proved by pathology were retrospectively reviewed in order to analyze the features of SCT during plain, corticomedullary and excretory phases. There were 83 males and 17 females, with a mean age of 54. 3 years ranging from 9 to 81 years.
There were 38 tumor masses in the left kidney and 62 in the right one. They were 1.0-3.0 cm (mean, 2.5 cm) in the greatest dimension. According to the 2004 WHO histological classification criteria for the tumors of the kidney. Seventy-six patients had clear cell renal cell carcinoma, 4 multilocular clear cell renal cell carcinomas, 9 papillary renal cell carcinoma, 4 chromophobe renal cell carcinomas and 7 unclassified renal cell carcinomas. Clear cell renal cell carcinoma exhibited rich blood supply and inhomogeneous density due to hemorrhage, necrosis or cystic degeneration. Multilocular clear cell renal cell carcinoma presented as a multilocular cystic mass with thin wall and septa, instead of an expansile nodule. Papillary renal cell carcinoma showed inhomogeneous density and hypovascular distribution. Chromophobe renal cell carcinoma was relatively homogeneous and hypovascular. Compared with clear cell renal cell carcinoma, unclassified renal cell carcinoma showed inhomogeneous density and hypervascular distribution with more invading growth features than the other subtypes.
Commonly encountered subtypes of the small renal cell carcinoma exhibit their own specific features in multiphasic spiral CT, which may be helpful in differential diagnosis, but each subtype should be differentiated from the renal oncocytoma, cystic nephroma, complex renal cyst, renal angiomyolipoma with minimal fat and renal infiltrating urothelial carcinoma.
探讨多期螺旋计算机断层扫描(SCT)在小肾癌鉴别诊断中的作用。
回顾性分析100例经病理证实的小肾癌(直径≤3.0 cm)患者的数据,以分析SCT平扫、皮质髓质期和排泄期的特征。其中男性83例,女性17例,平均年龄54.3岁,年龄范围为9至81岁。
左肾有38个肿瘤肿块,右肾有62个。肿瘤最大直径为1.0 - 3.0 cm(平均2.5 cm)。根据2004年世界卫生组织肾脏肿瘤组织学分类标准,76例为透明细胞肾细胞癌,4例为多房性透明细胞肾细胞癌,9例为乳头状肾细胞癌,4例为嫌色细胞肾细胞癌,7例为未分类肾细胞癌。透明细胞肾细胞癌血供丰富,因出血、坏死或囊性变而密度不均匀。多房性透明细胞肾细胞癌表现为薄壁和分隔的多房囊性肿块,而非膨胀性结节。乳头状肾细胞癌密度不均匀,血供少。嫌色细胞肾细胞癌相对均匀,血供少。与透明细胞肾细胞癌相比,未分类肾细胞癌密度不均匀,血供丰富,侵袭性生长特征比其他亚型更多。
小肾癌常见亚型在多期螺旋CT上表现出各自的特征,这可能有助于鉴别诊断,但各亚型均应与肾嗜酸细胞瘤、囊性肾瘤、复杂性肾囊肿、脂肪含量极少的肾血管平滑肌脂肪瘤及肾浸润性尿路上皮癌相鉴别。