UROLOGICAL SURVEY
Jinzaki M, Tanimoto A, Shinmoto H, Horiguchi Y, Sato K, Kuribayashi S, Silverman SG
Department of Diagnostic Radiology, Keio University School of Medicine, Tokyo, Japan
AJR Am J Roentgenol. 2007; 188: 9138
OBJECTIVE: In a small pilot study, we assessed whether earlyphase dynamic contrastenhanced MDCT can be used to detect bladder tumors and whether thin reconstruction improves the detection rate.
SUBJECTS AND METHODS: Thirtysix patients (30 with 59 cystoscopyproven bladder cancers and six with normal bladders) underwent dynamic contrastenhanced MDCT of the pelvis and abdomen. Images were obtained from the symphysis pubis to the diaphragm 70 seconds after injection of 100 mL of contrast medium. McNemar test was used to compare sensitivity per patient, segment, and tumor and specificity per patient and segment for each of three reconstruction methods: 5mm sections with no overlap (i.e., 5mm axial images), 2.5mm sections with 1.25mm overlap (i.e., thinsection axial images), and 2.5mm sections with 1.25mm overlap and multiplanar reformation (MPR) (i.e., thinsection axial images with MPR).
RESULTS: MDCT with a combination of thin, overlapped sections and MPR depicted all but one of 47 bladder tumors larger than 5 mm but only five of 12 tumors 5 mm or smaller. There were no falsepositive findings. Pertumor sensitivity was significantly better with thinsection images with MPR (90%) and thinsection images alone (86%) than with 5mm axial images (80%) (p < 0.05). Persegment sensitivity was significantly better with thinsection images with MPR (95%) and thinsection axial images alone (87%) than with 5mm axial images (79%) (p < 0.05). Perpatient sensitivity and perpatient and persegment specificity did not differ with the three methods.
CONCLUSION: Dynamic contrastenhanced MDCT of the pelvis shows promise for the detection of bladder tumors. Use of thinsection images with MPR and thinsection axial images alone had a significantly better rate of detection of bladder tumors than use of 5mm axial images.
Editorial Comment
The authors show the ability of thin (2.5 mm) and overlapped sections and multiplanar reconstruction (MPR) to depict small bladder tumors. Thinsection images (2.5 mm) with MPR were used to detect all but one of 47 bladder tumors larger than 5 mm but only five of 12 tumors 5 mm or smaller. There were no falsepositive findings. The sensitivity for detecting bladder tumors 5 mm or smaller was significantly better for thinsection images with MPR and thinsection axial images (both, 58%) than for 5mm axial images (25%) (p < 0.05). Use of thinsection axial images improved the detection rate only for tumors smaller than 5 mm. MPR improved the detection of tumor in the bladder dome and tumors adjacent to normal anatomic structures.
Multidetector CTurography has been shown to be an effective single comprehensive examination in the evaluation of patients with hematuria or with risk for the development of urothelial malignancies. Since protocols for MDCT urography varies from each institution, most MDCT urography images are obtained in the unenhanced phase (detection of calculi), nephrographicphase (detection of renal masses) and excretoryphase (detection of urothelial lesions). Some authors recommend that MDCT urography should be performed only after adequate cystoscopy since these protocols do not allow adequate evaluation of the bladder.
Since January 2006, we have been using in our institution similar technique described by the authors as part of MDCT urography (1). This additional phase of MDCTurography is used only in patients with macroscopic hematuria and with no previous cystoscopy. We agree with the authors that this "the bladderwall phase" (scans at 60 or 70 seconds after intravenous injection of contrast), allows the detection of small bladder tumors. However, we need to keep in mind that this additional phase cause significant increase in the effective radiation dose to the patients (18 to 25 mGy). For this reason, this protocol should be used with caution and primarily in older patients with macroscopic hematuria and absence of previous cystoscopy.
Reference
1. Kim JK, Park SY, Ahn HJ, Kim CS, Cho KS: Bladder cancer: analysis of multidetector row helical CT enhancement pattern and accuracy in tumor detection and perivesical staging. Radiology. 2004; 231: 72531.
Dr. Adilson Prando
Chief, Department of Radiology
Vera Cruz Hospital
Campinas, São Paulo, Brazil
Email: aprando@mpc.com.br
Can highattenuation renal cysts be differentiated from renal cell carcinoma at unenhanced CT?
Jonisch AI, Rubinowitz AN, Mutalik PG, Israel GM
Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA
Radiology. 2007; 243: 44550
PURPOSE: To retrospectively determine if renal cell carcinoma can be differentiated from highattenuation renal cysts at unenhanced computed tomography (CT) based on Hounsfield unit measurements and heterogeneity.
MATERIALS AND METHODS: The Human Investigation Committee at our institution approved this study with waiver of informed consent. This study was compliant with the HIPAA. Fiftyfour pathologically proved renal cell carcinomas in 54 patients (36 men and 18 women; average age, 53 years; range, 2390 years) and 56 highattenuation renal cysts in 51 patients (30 men and 21 women; average age, 63 years; range, 2886 years) were retrospectively evaluated at unenhanced CT. Two independent readers reviewed randomized unenhanced CT images and obtained Hounsfield unit readings of each mass. A subjective determination of lesion heterogeneity was also performed by using a fourpoint scale (1: homogeneous, 2: mildly heterogeneous, 3: moderately heterogeneous, 4: markedly heterogeneous). Statistical analysis was performed by using BlandAltman regression tree, classification and regression tree, and ShapiroWilk normality test.
RESULTS: The average attenuation of cysts for reader 1 was 53.4 HU (range, 23113 HU) and for reader 2 was 53.8 HU (range, 21108 HU). The average attenuation of neoplasms for reader 1 was 34.7 HU (range, 2160 HU) and for reader 2 was 38.4 HU (range, 2260 HU). For cyst heterogeneity, a score of 1 was given in 55 of 56 (98%) cysts for reader 1 and in 53 of 56 (95%) cysts for reader 2. For neoplasm heterogeneity, a score of 1 was given in 35 of 54 (65%) neoplasms for reader 1 and in 36 of 54 (67%) for reader 2. Given the distribution of cyst and tumor attenuation values and lesion heterogeneity, a homogeneous mass measuring 70 HU or greater at unenhanced CT has a greater than 99.9% chance of representing a highattenuation renal cyst.
CONCLUSION: The findings from this study may help differentiate highattenuation renal cysts from renal cell carcinomas at unenhanced CT and may suggest the next appropriate imaging study for definitive characterization.
Editorial Comment
A hyperdense cyst refers to a cyst that demonstrates high attenuation on nonenhanced CT scans. Hemorrhage or proteinaceous debris is the most common cause, but renal cell carcinoma may eventually demonstrate similar findings. A hyperdense renal cyst can be considered benign if it is sharply marginated or homogeneous or demonstrates a hematocrit effect on nonenhanced and contrastenhanced scan and demonstrates no significant enhancement on postcontrast scans. Because internal structures within a hyperdense renal cyst cannot be well evaluated by nonenhanced CT, US or MR imaging can be used for the differentiation. When sonography is performed, the mass is usually cystic but occasionally do not present all the sonographic criteria for a simple cyst. Actually internal septations and absence of posterior wall troughtransmission are frequently found.
The authors present an interesting observation, which should be useful for adequate characterization of hyperdense renal lesion found on nonenhanced CT scans particularly in those patients submitted to a noncontrast CT scans for the detection of urolithiasis. They found that the attenuation of a renal mass and its degree of heterogeneity are useful findings in distinguishing a highattenuation renal cyst from renal cell carcinoma on unenhanced CT images. If the density of the mass is greater than 70 HU and the mass is homogeneous, there is a chance of almost 100% (99.9%) that the mass is benign hyperdense renal cyst. They concluded that in this situation there is no need for contrast enhanced CT scan and highresolution US studies or MR imaging can be used as complimentary test.
Dr. Adilson Prando
Chief, Department of Radiology
Vera Cruz Hospital
Campinas, São Paulo, Brazil
Email: aprando@mpc.com.br
Imaging
Publication Dates
-
Publication in this collection
29 Aug 2007 -
Date of issue
June 2007