Pickhardt P J, Siegel C L, McLarney J K
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
AJR Am J Roentgenol. 2001 Mar;176(3):627-33. doi: 10.2214/ajr.176.3.1760627.
Collecting duct carcinoma derives from the renal medulla and has an infiltrative growth pattern at pathologic examination. The purpose of our study was to characterize the imaging features of this aggressive malignancy and determine whether the diagnosis can be reliably suggested from imaging findings.
Radiologic studies from 17 patients with pathologically proven collecting duct carcinoma were analyzed by two reviewers.
The tumors varied in size from 1.5 to 19 cm (mean, 7.7 cm). Medullary involvement was present on CT in 16 (94%) of 17 cases, but cortical involvement or an exophytic component was also present in 15 cases (88%) and 10 cases (59%), respectively. The reniform contour of the kidney was preserved in seven cases (41%) and correlated with a smaller tumor size (p<0.01). Tumors showed an infiltrative appearance on CT in 11 cases (65%), but an expansile component was also present in eight of these cases. A cystic component was present on CT in six (35%) of 17 cases. On sonography, the solid tumor component was hyperechoic to normal renal parenchyma in six of seven cases and isoechoic in the other. On MR imaging, all tumors (4/4) were hypointense on T2-weighted imaging. On urography, all lesions (5/5) distorted the intrarenal collecting system. On angiography, all tumors (3/3) were hypovascular.
Medullary involvement and an infiltrative appearance are common findings on cross-sectional imaging and may suggest the diagnosis of collecting duct carcinoma. In large tumors, however, these features are frequently overshadowed by an exophytic or expansile component that cannot be distinguished from the more common cortical renal cell carcinoma.
集合管癌起源于肾髓质,病理检查显示为浸润性生长模式。本研究的目的是描述这种侵袭性恶性肿瘤的影像学特征,并确定能否从影像学表现可靠地做出诊断。
两名阅片者分析了17例经病理证实为集合管癌患者的影像学研究资料。
肿瘤大小从1.5厘米至19厘米不等(平均7.7厘米)。17例中有16例(94%)在CT上显示有髓质受累,但也分别有15例(88%)和10例(59%)存在皮质受累或外生性成分。7例(41%)肾脏保留了肾形轮廓,且与较小的肿瘤大小相关(p<0.01)。11例(65%)肿瘤在CT上表现为浸润性,但其中8例也有膨胀性成分。17例中有6例(35%)在CT上有囊性成分。在超声检查中,7例中的6例实性肿瘤成分相对于正常肾实质为高回声,另1例为等回声。在磁共振成像上,所有肿瘤(4/4)在T2加权成像上均为低信号。在尿路造影上,所有病变(5/5)均使肾内集合系统变形。在血管造影上,所有肿瘤(3/3)均为低血供。
髓质受累和浸润性表现是横断面成像上的常见表现,可能提示集合管癌的诊断。然而,在大肿瘤中,这些特征常被外生性或膨胀性成分掩盖,无法与更常见的皮质肾细胞癌区分开来。