Early and very early hepatocellular carcinoma: when and how much do staging and choice of treatment really matter? A multi-center study. (73/2185)

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Do patients undergo prostate examination while having a colonoscopy? (74/2185)

OBJECTIVES: To determine the rate at which physicians report performing a digital rectal examination and comment on the prostate gland before performing colonoscopy in men 50 to 70 years of age. METHODS: A retrospective chart review of all men 50 to 70 years of age who had a colonoscopy in Kingston, Ontario, in 2005 was completed. It was noted whether each physician described performing a digital rectal examination before the colonoscopy, and if so, whether he or she commented on the prostate. RESULTS: In 2005, 846 eligible colonoscopies were performed by 17 physicians in Kingston, Ontario. In 29.2% of cases, the physician made no comment about having performed a digital rectal examination; in 55.8% of cases, the physician commented on having completed a digital rectal examination but said nothing about the prostate; and in 15.0% of cases, the physician made a comment regarding the prostate. No physician consistently commented on the prostate for all patients, and in no circumstances was direct referral to another physician or follow-up suggested. DISCUSSION: A colonoscopy presents an ideal opportunity for physicians to use a digital rectal examination to assess for prostate cancer. Physicians performing colonoscopies in men 50 to 70 years of age should pay special attention to the prostate while performing a digital rectal examination before colonoscopy. This novel concept may help maximize resources for cancer screening and could potentially increase the detection rate of clinically palpable prostate cancer.  (+info)

Automated regional registration and characterization of corresponding microcalcification clusters on temporal pairs of mammograms for interval change analysis. (75/2185)

A computerized regional registration and characterization system for analysis of microcalcification clusters on serial mammograms is being developed in our laboratory. The system consists of two stages. In the first stage, based on the location of a detected cluster on the current mammogram, a regional registration procedure identifies the local area on the prior that may contain the corresponding cluster. A search program is used to detect cluster candidates within the local area. The detected cluster on the current image is then paired with the cluster candidates on the prior image to form true (TP-TP) or false (TP-FP) pairs. Automatically extracted features were used in a newly designed correspondence classifier to reduce the number of false pairs. In the second stage, a temporal classifier, based on both current and prior information, is used if a cluster has been detected on the prior image, and a current classifier, based on current information alone, is used if no prior cluster has been detected. The data set used in this study consisted of 261 serial pairs containing biopsy-proven calcification clusters. An MQSA radiologist identified the corresponding clusters on the mammograms. On the priors, the radiologist rated the subtlety of 30 clusters (out of the 261 clusters) as 9 or 10 on a scale of 1 (very obvious) to 10 (very subtle). Leave-one-case-out resampling was used for feature selection and classification in both the correspondence and malignant/benign classification schemes. The search program detected 91.2% (238/261) of the clusters on the priors with an average of 0.42 FPs/image. The correspondence classifier identified 86.6% (226/261) of the TP-TP pairs with 20 false matches (0.08 FPs/image) relative to the entire set of 261 image pairs. In the malignant/benign classification stage the temporal classifier achieved a test A(z) of 0.81 for the 246 pairs which contained a detection on the prior. In addition, a classifier was designed by using the clusters on the current mammograms only. It achieved a test A(z) of 0.72 in classifying the clusters as malignant and benign. The difference between the performance of the temporal classifier and the current classifier was statistically significant (p=0.0014). Our interval change analysis system can detect the corresponding cluster on the prior mammogram with high sensitivity, and classify them with a satisfactory accuracy.  (+info)

Quantification of breast density with dual energy mammography: a simulation study. (76/2185)

Breast density, the percentage of glandular breast tissue, has been identified as an important yet underutilized risk factor in the development of breast cancer. A quantitative method to measure breast density with dual energy imaging was investigated using a computer simulation model. Two configurations to measure breast density were evaluated: the usage of monoenergetic beams and an ideal detector, and the usage of polyenergetic beams with spectra from a tungsten anode x-ray tube with a detector modeled after a digital mammography system. The simulation model calculated the mean glandular dose necessary to quantify the variability of breast density to within 1/3%. The breast was modeled as a semicircle 10 cm in radius with equal homogenous thicknesses of adipose and glandular tissues. Breast thicknesses were considered in the range of 2-10 cm and energies in the range of 10-150 keV for the two monoenergetic beams, and 20-150 kVp for spectra with a tungsten anode x-ray tube. For a 4.2 cm breast thickness, the required mean glandular doses were 0.183 microGy for two monoenergetic beams at 19 and 71 keV, and 9.85 microGy for two polyenergetic spectra from a tungsten anode at 32 and 96 kVp with beam filtrations of 50 microm Rh and 300 microm Cu for the low and high energy beams, respectively. The results suggest that for either configuration, breast density can be precisely measured with dual energy imaging requiring only a small amount of additional dose to the breast. The possibility of using a standard screening mammogram as the low energy image is also discussed.  (+info)

An EM approach to MAP solution of segmenting tissue mixture percentages with application to CT-based virtual colonoscopy. (77/2185)

Electronic colon cleansing (ECC) is an emerging technique developed to segment the colon lumen from a patient's abdominal computed tomography colonography (CTC) images. However, the residue stool and fluid tagged by contrast materials as well as mixed tissue distribution with partial volume (PV) effect impose several challenges for ECC, resulting in incomplete and overcomplete cleansings. To address the PV effect, this work investigated an improved maximum a posteriori expectation-maximization (MAP-EM) image segmentation algorithm which simultaneously estimates tissue mixture percentages within each image voxel and statistical model parameters for the tissue distribution. Given the segmented tissue mixture information beyond the image voxel level, not only the PV effect has been satisfactorily addressed as a particular case of tissue mixture problem, but incomplete and overcomplete ECC causes could also be maximally avoided. For clinical application to CTC that involves several issues transferring from theoretical analysis to practical validation, an innovative initialization procedure and refined estimation strategy were proposed to build an ECC pipeline based on the MAP-EM segmentation. The pipeline was evaluated based on 52 patient CTC studies, downloaded from the website of the Virtual Colonoscopy Screening Resource Center, by two radiologists. A noticeable improvement over the authors' previous ECC pipeline was documented. Several typical cases were also presented to show visually the improved performance of the presented ECC pipeline.  (+info)

Establishing the added benefit of measuring MMP9 in FOB positive patients as a part of the Wolverhampton colorectal cancer screening programme. (78/2185)

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Human papillomavirus type 18 DNA load and 2-year cumulative diagnoses of cervical intraepithelial neoplasia grades 2-3. (79/2185)

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Monoclonal gammopathy of undetermined significance (MGUS) consistently precedes multiple myeloma: a prospective study. (80/2185)

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