<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/"><channel rdf:about="http://www.clinicalimaging.org/?rss=yes"><title>Clinical Imaging</title><description>Clinical Imaging RSS feed: Current Issue. 
 Clinical Imaging  provides comprehensive coverage of new technology, new applications, and important issues concerning all diagnostic 
imaging methods. Under the editorship of Joseph P. Whalen, M.D.,  Clinical Imaging  explores the relative merits of established 
and developing diagnostic imaging technology, with regard to cost effectiveness, safety, and propriety where specific disorders and physiological 
systems are concerned.
The journal publishes: 
 • Original articles – peer–reviewed reports of new clinical developments

 
 • "Radiology Pathology Conference" features – a brief clinical history with physical findings, followed by a discussion 
of the radiologic imagings with a detailed correlation of the pathological findings 
 • Review articles – an overview of 
a key topic, with an invited editorial on the same subject 
 • Case reports – limited to important new observations 
 • 
Abstracts – summaries of significant papers in related journals 
 • Book Reviews 
 From ultrasound to MRI,  Clinical 
Imaging  provides essential information for radiologists, radiology residents, and radiologic technologists.</description><link>http://www.clinicalimaging.org/?rss=yes</link><dc:publisher>Elsevier Inc.</dc:publisher><dc:language>en</dc:language><dc:rights> © 2010 Published by Elsevier Inc. All rights reserved. </dc:rights><prism:publicationName>Clinical Imaging</prism:publicationName><prism:issn>0899-7071</prism:issn><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:publicationDate>March 2010</prism:publicationDate><prism:copyright> © 2010 Published by Elsevier Inc. All rights reserved. </prism:copyright><prism:rightsAgent>healthpermissions@elsevier.com</prism:rightsAgent><items><rdf:Seq><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707110000239/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001685/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109002332/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109000886/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003611/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001156/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001995/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001107/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109000606/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001259/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001247/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109002344/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001740/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109001193/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS089970710900117X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003192/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003222/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003209/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003210/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003246/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003258/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS089970710900326X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003271/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003283/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003295/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003301/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003313/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003325/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003337/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003349/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003350/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003362/abstract?rss=yes"/><rdf:li rdf:resource="http://www.clinicalimaging.org/article/PIIS0899707109003374/abstract?rss=yes"/></rdf:Seq></items></channel><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707110000239/abstract?rss=yes"><title>Contents</title><link>http://www.clinicalimaging.org/article/PIIS0899707110000239/abstract?rss=yes</link><description></description><dc:title>Contents</dc:title><dc:creator></dc:creator><dc:identifier>10.1016/S0899-7071(10)00023-9</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section></prism:section><prism:startingPage>i</prism:startingPage><prism:endingPage>ii</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001685/abstract?rss=yes"><title>Myocardial bridging on dual-source computed tomography: degree of systolic compression of mural coronary artery correlating with length and depth of the myocardial bridge</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001685/abstract?rss=yes</link><description>Abstract: Objective: To investigate the correlation between the degree of systolic compression of mural coronary artery (MCA) and the length and depth of myocardial bridging (MB) with dual-source computed tomography (DSCT).Methods: The length and depth of MB were measured from diastolic phase. All datasets were reconstructed in 5% steps of R-R interval. The optimum phases were chosen where the maximal and minimal diameters were shown. The degree of systolic compression of MCA was calculated. The correlation between length and depth of MB and the degree of systolic compression of MCA were analyzed by Pearson test.Results: The minimal diameters were found in 27 sites (90.0%) from 30% to 35% R-R interval, and the maximal diameters were found in 27 sites (90.0%) from 70% to 80% R-R interval. The correlation between systolic compression of MCA and length of MB was not significant (r=0.096, P=.613); however, the correlation between systolic compression of MCA and the depth of MB was significant (r=0.675, P&lt;.01).Conclusion: The minimal and maximal diameters of MCA are usually demonstrated in 30–35% and 70–80% R-R reconstruction interval, respectively. The degree of systolic compression of MCA correlates well with the depth of MB.</description><dc:title>Myocardial bridging on dual-source computed tomography: degree of systolic compression of mural coronary artery correlating with length and depth of the myocardial bridge</dc:title><dc:creator>Shi-he Liu, Qing Yang, Jiu-hong Chen, Xi-ming Wang, Min Wang, Cheng Liu</dc:creator><dc:identifier>10.1016/j.clinimag.2009.05.010</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-08-28</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-08-28</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>83</prism:startingPage><prism:endingPage>88</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109002332/abstract?rss=yes"><title>Diffusion-weighted MRI evaluation of breast cancer extension</title><link>http://www.clinicalimaging.org/article/PIIS0899707109002332/abstract?rss=yes</link><description>Abstract: Aim: To investigate the feasibility of using diffusion-weighted MR imaging (DWI) to accurately measure breast cancer extension.Materials and Methods: The extensions of 59 breast lesions were investigated on DW images and apparent diffusion coefficient (ADC) maps and compared to the pathological exams.Results: Three groups were observed: accurate, overdiagnosis, and false negative. There were no significant differences seen in accurate or false-negative group when b was 500 and 1000 s/mm2 when two lesions in the overdiagnosis group at both b values.Conclusion: DWI and the ADC value have potential for evaluating cancer extension.</description><dc:title>Diffusion-weighted MRI evaluation of breast cancer extension</dc:title><dc:creator>Qiu Long-Hua, Xiao Qin, Yang Wen-Tao, Tang Feng, Shen Kun-Wei, Wu Bin, Gu Ya-Jia</dc:creator><dc:identifier>10.1016/j.clinimag.2009.09.002</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-10-26</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-10-26</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>89</prism:startingPage><prism:endingPage>96</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109000886/abstract?rss=yes"><title>Low-cost phantoms for training of stereotactic vacuum-assisted biopsy of the breast</title><link>http://www.clinicalimaging.org/article/PIIS0899707109000886/abstract?rss=yes</link><description>Abstract: To test low-cost phantoms for training in stereotactic breast biopsy, we prepared eggplant with calcium powder; gelatin and turkey breast with coarse salt, peppercorns, and calcium powder, respectively; and short-bread pastry with salt. Three to 12 cores were harvested with an 11-gauge vacuum biopsy unit. Mammography images were taken before and after biopsy and from the biopsy cores.The pastry phantom provided the best simulation of microcalcifications for stereotactic biopsy with realistic cores, long durability, and short preparation time.</description><dc:title>Low-cost phantoms for training of stereotactic vacuum-assisted biopsy of the breast</dc:title><dc:creator>Arne Fischmann, Katja C. Siegmann</dc:creator><dc:identifier>10.1016/j.clinimag.2009.03.011</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-05-20</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-05-20</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>97</prism:startingPage><prism:endingPage>99</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003611/abstract?rss=yes"><title>Multimodality imaging of usual and unusual sites of metastasis which occur after definitive therapy for rectal cancer</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003611/abstract?rss=yes</link><description>Abstract: Rectal cancer is a common malignancy encountered largely after the fifth decade of life. Due to the recent advances in cancer therapy, which include chemoradiation therapy pre- and postoperatively, survival has improved. Radiologist has become an integral part of the patient management team to diagnose and localize the area of recurrent rectal cancer. Although typical pathways of rectal cancer spread have been described, recurrence may occur in unexpected locations due to the currently available aggressive therapy being able to control local disease. Imaging surveillance should include careful evaluation of expected and unexpected anatomic sites where tumor may recur. This paper will describe the common and uncommon locations of recurrent rectal cancer.</description><dc:title>Multimodality imaging of usual and unusual sites of metastasis which occur after definitive therapy for rectal cancer</dc:title><dc:creator>Priya Bhosale, Janio Szklaruk, Revathy Iyer</dc:creator><dc:identifier>10.1016/j.clinimag.2007.12.012</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-01-15</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-01-15</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>100</prism:startingPage><prism:endingPage>108</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001156/abstract?rss=yes"><title>Positive correlation between serum liver enzyme levels and standard uptake values of liver on FDG-PET</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001156/abstract?rss=yes</link><description>Abstract: Purpose: The aim of the study is to assess the relationship between serum liver enzyme level, hepatic virus infectious state, and standard uptake value of liver on 2-fluoro-2-deoxy-D-glucose (FDG)-positron emission tomography (PET).Material and Methods: It is the retrospective review study from September 2005 to September 2007. A total of 354 healthy subjects referred from the Department of Community Medicine and Health Examination Center of our hospital for health screening were reviewed retrospectively and recruited for analysis. Whole-body FDG-PET, serum liver enzyme levels [aspartate aminotransferase (AST) or SGOT and alanine aminotransferase (ALT) or SGPT], and hepatic B (HBV)/hepatic C virus (HCV) infectious states by checking serum antibodies were performed in all subjects. The mean and maximal values of standard uptake values (SUV) of liver were calculated. The relationships between serum liver enzyme levels, hepatic virus infectious states, and standard uptake values of liver on FDG-PET were evaluated.Result: There is statistically significant positive correlation between SGOT/SGPT and SUV of liver on FDG-PET. However, there are no significant differences in the SUV of liver on FDG-PET between HBV/HCV infection and nonhepatic virus infection subjects.Conclusion: High FDG uptake in the liver because of high level of SGOT/SGPT may lower the diagnostic sensitivity of hepatic malignant or infectious lesions on FDG-PET. For avoiding false-negative findings, careful evaluation of liver on FDG-PET and correlation with other clinical manifestations should be recommended in patients with high level of SGOT/SGPT. Nevertheless, neither HBV/HCV infectious states significantly influences on the SUV of liver on FDG-PET.</description><dc:title>Positive correlation between serum liver enzyme levels and standard uptake values of liver on FDG-PET</dc:title><dc:creator>Chun Y. Lin, Hueisch J. Ding, Tsann Lin, Cheng C. Lin, Tsung H. Kuo, Chia H. Kao</dc:creator><dc:identifier>10.1016/j.clinimag.2009.05.007</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-07-23</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-07-23</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>109</prism:startingPage><prism:endingPage>112</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001995/abstract?rss=yes"><title>Endometriosis following cesarean section: ultrasonography and magnetic resonance imaging</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001995/abstract?rss=yes</link><description>Abstract: We present three cases of endometriosis developing in the abdominal wall following cesarean section.The patients were examined by Doppler ultrasonography (US) and magnetic resonance imaging (MRI). The object is to describe the US and MRI findings of the lesion and evaluate their role in the diagnosis and management.In our opinion, a single procedure is sufficient in evaluating the lesion and in reaching the diagnosis.</description><dc:title>Endometriosis following cesarean section: ultrasonography and magnetic resonance imaging</dc:title><dc:creator>Anja Randriamarolahy, Hubert Perrin, Jean Michel Cucchi, Françoise Fuerxer, Philippe Brunner, Jean Noël Bruneton</dc:creator><dc:identifier>10.1016/j.clinimag.2009.08.025</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-01-06</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-01-06</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>113</prism:startingPage><prism:endingPage>115</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001107/abstract?rss=yes"><title>Imaging findings of femoroacetabular impingement syndrome: focusing on mixed-type impingement</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001107/abstract?rss=yes</link><description>Abstract: The aim of our study was to analyze the imaging findings of femoroacetabular impingement (FAI). Eight consecutive patients [age range, 19–46 years (mean, 28.6 years); M/F ratio=7:1] who underwent operation for FAI were analyzed. We analyzed bump, acetabular retroversion and protrusion, and osteoarthritis in the radiographs. In MR arthrography, we analyzed α-angle, anterolateral labral tear, cartilage abnormality, herniation pit, paralabral cyst, subchondral cyst, and marrow edema. We correlated the imaging findings with operative findings. In the radiographs, all eight patients showed bump and osteoarthritis (Kellgren–Lawrence score II–IV), and five (62.5%) patients showed acetabular retroversion. In MR arthrography, anterolateral labral tear and mild cartilage abnormality (Outerbridge grade I and II) were seen in all eight patients; increased α-angle was seen in six cases (75%). Anterolateral labral tear, bump, and mild cartilage abnormality were seen in all eight patients during operation. According to the above findings, we divided the patients into three cam-type and five mixed-type FAI. In the five mixed-type FAI, both bump and acetabular retroversion were seen. The mixed-type FAI is the most prevalent type in our study. The main imaging findings of mixed-type FAI were acetabular retroversion, bump, and early osteoarthritis in radiographs, and anterolateral labral tear, cartilage abnormality, and increased α-angle in MR arthrography.</description><dc:title>Imaging findings of femoroacetabular impingement syndrome: focusing on mixed-type impingement</dc:title><dc:creator>Suk-Joo Hong, Won Yong Shon, Chang Yoon Lee, Jae Sung Myung, Chang Ho Kang, Baek Hyun Kim</dc:creator><dc:identifier>10.1016/j.clinimag.2009.04.025</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-06-22</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-06-22</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>116</prism:startingPage><prism:endingPage>120</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109000606/abstract?rss=yes"><title>Papillary thyroid carcinoma on sonography</title><link>http://www.clinicalimaging.org/article/PIIS0899707109000606/abstract?rss=yes</link><description>Abstract: Objective: The purpose of this study is to investigate the characteristics of papillary thyroid carcinomas (PTCs) on color duplex sonography (CDUS).Methods: We retrospectively reviewed 115 nodules (104 patients) with PTC confirmed by pathology from February 1, 2005, to August 31, 2008. The size, border, calcification, echotexture, hemodynamics (peak systolic velocity and resistance index) of the thyroid nodules and cervical lymph nodes on CDUS were analyzed.Results: There was a close relationship between the size of the nodule and the vascularity of the thyroid carcinoma (P=.000). Microcalcification increased the suspicion for malignancy of the thyroid nodule. A hypoechoic thyroid nodule with abundant internal vascularity, ill-defined border and microcalcification was highly suggested PTC.Conclusion: CDUS plays an important role in the early detection of PTC and cervical lymph node metastasis, which would provide surgeons with valuable information for planning surgical intervention. Mastering manifestations of PTC on CDUS will improve the accuracy in the diagnosis of PTC. CDUS-guided fine needle aspiration of the thyroid nodule is the standard in the diagnosis of thyroid carcinoma and metastasis pre- and postthyroidectomy.</description><dc:title>Papillary thyroid carcinoma on sonography</dc:title><dc:creator>Quan-shui Li, Sheng-hua Chen, Hua-hua Xiong, Xiao-hua Xu, Zhen-zhou Li, Guo-qiang Guo</dc:creator><dc:identifier>10.1016/j.clinimag.2009.03.003</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-05-25</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-05-25</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>121</prism:startingPage><prism:endingPage>126</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001259/abstract?rss=yes"><title>Positive predictive values of sonographic features of solid thyroid nodule</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001259/abstract?rss=yes</link><description>Abstract: Aim: The purpose of this study was to assess the positive predictive value of the suspicious sonographic features of solid nodules of the thyroid.Materials and methods: After approval by our institutional review board, we evaluated 594 sonographically detected nodules on which fine needle aspiration biopsy had been performed from January to December 2005. Among these, pure cystic lesions and inadequate pathologic results were excluded. The remaining 530 solid thyroid nodules were analyzed by two radiologists. Each lesion was classified based on four sonographic features that suggested malignancy: microcalcifications; an irregular or microlobulated margin; marked hypoechogenicity; and a shape that was taller than wide. The sensitivity, specificity, positive predictive value, and negative predictive value of the each sonographic feature were calculated.Results: Final pathologic results showed that 97 (18.3%) of 530 nodules were malignant. The positive predictive values for malignancy in each sonographic feature were microcalcifications, 38.6% (39/101); an irregular or microlobulated margin, 28.2% (70/248); marked hypoechogenecity, 49.4% (38/77); taller than wide shape, 59.8% (49/82). In terms of relative risk, microcalcification [P&lt;.01, relative risk (RR)=3.115, 95% CI: 1.724–5.628], hypoechogenecity (P&lt;.01, RR=2.510, 95% CI: 1.290–4.881). The shape of nodule which was taller than wide (P&lt;.01, RR=7.624, 95% CI: 4.156–13.986) revealed the highest predictive sonographic finding suggesting malignancy. However, margin is the least significant feature of detection of thyroid malignancy (P=.27, RR=1.395, 95% CI: 0.777–2.505).Conclusion: The three sonographic features of solid thyroid nodule, that is, microcalcifications, marked hypoechogenecity, and a taller than wide shape are meaningful findings in the diagnosis of thyroid malignancy. The shape that was taller than wide was the most reliable sonographic feature for predicting malignancy.</description><dc:title>Positive predictive values of sonographic features of solid thyroid nodule</dc:title><dc:creator>Yoo Jin Hong, Eun Ju Son, Eun-Kyung Kim, Jin Young Kwak, Soon Won Hong, Hang-Seok Chang</dc:creator><dc:identifier>10.1016/j.clinimag.2008.10.034</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-09-14</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-09-14</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Original Articles</prism:section><prism:startingPage>127</prism:startingPage><prism:endingPage>133</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001247/abstract?rss=yes"><title>Bilateral thalamic infarction—a rare manifestation of dural venous sinus thrombosis</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001247/abstract?rss=yes</link><description>Abstract: Bilateral infarctions of the thalamus account for only a small fraction of ischemic strokes and carry a poor prognosis. These infarcts rarely have a venous etiology. A case secondary to straight sinus thrombosis is presented. Difficulties in considering the diagnosis and its radiological appearances are discussed. A simple imaging pathway including computed tomographic angiography and magnetic resonance imaging including a susceptibility-weighted sequence is presented in order to facilitate determination of the exact etiology in order to optimize therapy accordingly.</description><dc:title>Bilateral thalamic infarction—a rare manifestation of dural venous sinus thrombosis</dc:title><dc:creator>Johannes Gossner, Jörg Larsen, Michael Knauth</dc:creator><dc:identifier>10.1016/j.clinimag.2009.05.008</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-08-12</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-08-12</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>134</prism:startingPage><prism:endingPage>137</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109002344/abstract?rss=yes"><title>CT and MR imaging of Susac syndrome in a young male presenting with acute disorientation</title><link>http://www.clinicalimaging.org/article/PIIS0899707109002344/abstract?rss=yes</link><description>Abstract: Susac syndrome is a rare neurologic disorder first described by Susac et al. in 1979. Clinically, Susac syndrome consists of a triad including encephalopathy, branch retinal artery occlusion, and sensorineural hearing loss. Microinfarction is believed to be the basic histologic feature and MR is considered the best imaging modality. This case documents the typical imaging findings of Susac syndrome, as well as the unique MR imaging finding of cranial nerve enhancement.</description><dc:title>CT and MR imaging of Susac syndrome in a young male presenting with acute disorientation</dc:title><dc:creator>Andrew M. Allmendinger, Vadim Spektor, Sylvie Destian</dc:creator><dc:identifier>10.1016/j.clinimag.2009.09.003</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-10-26</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-10-26</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>138</prism:startingPage><prism:endingPage>142</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001740/abstract?rss=yes"><title>Use of diffusion-weighted imaging in recurrent central nervous system Whipple's disease: a case report and review of the literature</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001740/abstract?rss=yes</link><description>Abstract: A case of Whipple's disease with development of antibiotic resistance is reported. The patient's symptomatology correlated with evolution of diffusion abnormality rather than with lesion enhancement. The lesion demonstrated no hyperperfusion, moderately elevated choline, and decreased N-acetylaspartate.Conventional magnetic resonance (MR) imaging findings of central nervous system Whipple's disease are nonspecific and may mimic neoplasm. MR perfusion and spectroscopy findings are reported, which may assist in diagnosis. Change in diffusion restriction appears to be a potential imaging indicator of clinical progression and response to therapy.</description><dc:title>Use of diffusion-weighted imaging in recurrent central nervous system Whipple's disease: a case report and review of the literature</dc:title><dc:creator>Amit A. Raheja, Yvonne W. Lui, Alberto Pinzon-Ardila, Ruth P. Lim, Steven A. Sparr</dc:creator><dc:identifier>10.1016/j.clinimag.2009.05.011</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-09-17</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-09-17</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>143</prism:startingPage><prism:endingPage>147</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109001193/abstract?rss=yes"><title>Radiologic appearance of a bronchial granular cell tumor with secondary obstructive changes</title><link>http://www.clinicalimaging.org/article/PIIS0899707109001193/abstract?rss=yes</link><description>Abstract: Bronchial granular cell tumor is a rare neoplasm. This report describes a 16-year-old female with this tumor in the right upper lobe. An ill-defined mass with peripheral infiltration was recognized on a chest radiograph. Thoracic computed tomography showed an intrabronchial mass lesion at the proximal portion of the bronchial bifurcation of the right B1 segment. The tumor completely occluded the bronchial lumen and thus caused obstructive changes of the lung distal to the tumor.</description><dc:title>Radiologic appearance of a bronchial granular cell tumor with secondary obstructive changes</dc:title><dc:creator>Naoki Kutuya, Aoi Akiduki</dc:creator><dc:identifier>10.1016/j.clinimag.2009.05.003</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-07-16</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-07-16</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>148</prism:startingPage><prism:endingPage>151</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS089970710900117X/abstract?rss=yes"><title>Solid pseudopapillary tumor of the pancreas in children: typical radiological findings and pathological correlation</title><link>http://www.clinicalimaging.org/article/PIIS089970710900117X/abstract?rss=yes</link><description>Abstract: We report a case series of three children with solid pseudopapillary tumor of the pancreas (SPT) in which a complete radiological work-up, including ultrasound, computed tomography scans, and MRI, has been carried out. The aim of this article is to highlight the characteristic imaging findings of SPT in the pediatric age group and to establish a correlation with typical histopathological findings of the lesion.</description><dc:title>Solid pseudopapillary tumor of the pancreas in children: typical radiological findings and pathological correlation</dc:title><dc:creator>Saad Al-Qahtani, Francois Gudinchet, Tarek Laswed, Pierre Schnyder, Sabine Schmidt, Maria-Chiara Osterheld, Leonor Alamo</dc:creator><dc:identifier>10.1016/j.clinimag.2009.06.024</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2009-08-28</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2009-08-28</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>152</prism:startingPage><prism:endingPage>156</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003192/abstract?rss=yes"><title>Case reports</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003192/abstract?rss=yes</link><description></description><dc:title>Case reports</dc:title><dc:creator></dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.003</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Case Reports</prism:section><prism:startingPage>157</prism:startingPage><prism:endingPage>157</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003222/abstract?rss=yes"><title></title><link>http://www.clinicalimaging.org/article/PIIS0899707109003222/abstract?rss=yes</link><description>Cardiac Imaging Direct Diagnosis in Radiology is one of a series named Dx-Direct composed of 12 Thieme books covering the main subspecialties in radiology such as gastrointestinal, musculoskeletal, and interventional radiology. The aim of the “Dx-Direct” is not to present and describe all possible cardiovascular diseases but only the cases radiologists are most likely to see in their typical working day. All the books in the series discuss each condition or disease following the same format: Definitions (Epidemiology, Etiology), Imaging Signs, Clinical Aspects (Typical Presentation, Treatment Options, Course and Prognosis), Differential Diagnosis and key References. All sections are well balanced, easy and fast to read, with just the right level of detail. Since cardiac imaging has typically a multimodality approach, it is worthy of notice to begin each Imaging Sign section indicating the modality of choice which would allow the reader to reach the right diagnosis. Particularly valuable are the What Does the Clinician Want to Know and the Tips and Pitfalls Sections, presented at the end of each case, that discuss those aspects with simplicity, frequently introducing the main clinical data not to be forgotten by the radiologist. The key references are comprehensive and updated.</description><dc:title></dc:title><dc:creator>Pietro Torricelli</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.006</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-01-25</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-01-25</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Book Reviews</prism:section><prism:startingPage>158</prism:startingPage><prism:endingPage>158</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003209/abstract?rss=yes"><title></title><link>http://www.clinicalimaging.org/article/PIIS0899707109003209/abstract?rss=yes</link><description>In the last decade, we have seen a diffusion and an exponential growth of diagnostic metabolic imaging by PET and PET/CT, particularly in oncology. This imaging modality has revolutionized and improved the management and sometimes the treatment of several pathologies, not only in oncology. The main reason for its success is that by PET we can image biological functions instead of anatomy. Consequently, nowadays, PET/CT in joining the morphological and functional imaging has, in many cases, replaced conventional CT as an essential diagnostic medium in managing patients with cancer, neurological diseases, and cardiovascular disorders.</description><dc:title></dc:title><dc:creator>Eugenio Borsatti</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.004</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-01-25</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-01-25</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Book Reviews</prism:section><prism:startingPage>158</prism:startingPage><prism:endingPage>159</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003210/abstract?rss=yes"><title></title><link>http://www.clinicalimaging.org/article/PIIS0899707109003210/abstract?rss=yes</link><description>In this voluminous textbook, the objective of the authors is to help the readers, in particular the gastrointestinal radiologists facing problematic abdominal images, in reaching the correct diagnosis. The book is subdivided into five sections: the first one, “Advanced Modalities as Problem-Solving Tool,” discusses in four chapters the role of ultrasonography, multidetector computed tomography, magnetic resonance imaging, and positron emission tomography. The fifth chapter concludes this section with a very informative review of “A Multidimensional Approach to Abdominal Imaging.” Section 2, “Problem Solving: Disease Categories,” deals with localization and spread of disease; emphasizes the point that often the pathologic process is not localized to a specific organ and its origin may be removed from its present localization; and discusses the discovery by computed tomography of small incidentalomas, incidental asymptomatic lesions, and how to follow them. In “Imaging Evaluation of Acute Abdominal Pain,” the authors review the numerous possible causes and the related different diagnostic conclusions. The chapter “Imaging Evaluation of Trauma” presents the role of the different imaging procedures in the study of a trauma, wherever its location in the abdominal cavity. In “A Brief Guide to Cancer Imaging,” the staging and spread of malignant tumors involving the abdomen and pelvis are discussed. This section ends with a chapter dealing with common inherited and metabolic disorders.</description><dc:title></dc:title><dc:creator>Antonio F. Govoni</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.005</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Book Reviews</prism:section><prism:startingPage>159</prism:startingPage><prism:endingPage>159</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003246/abstract?rss=yes"><title>Imaging features of cavernous hemangiomas of the orbit [in French]</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003246/abstract?rss=yes</link><description>Cavernous hemangioma is the most frequent benign tumor of the orbit. The clinical presentation is that of a slowly progressive intra-orbital mass with variable degrees of exophthalmos. CT typically demonstrates the presence of a well-defined oval or rounded shaped mass but MRI provides superior evaluation of the orbit. The tumor is intra-conal in 80% of cases and usually shows TlW hypo-intensity, T2W hyperintensity and heterogeneous contrast enhancement that becomes more homogeneous on delayed imaging (5 minutes).</description><dc:title>Imaging features of cavernous hemangiomas of the orbit [in French]</dc:title><dc:creator>B. Dallaudiere, Y. Benayoun, M.P. Boncoeur-Martel, P.Y. Robert, J.P. Adenis</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.008</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>160</prism:startingPage><prism:endingPage>160</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003258/abstract?rss=yes"><title>Specimen radiographs assist in identifying and assessing resection margins of occult breast carcinomas</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003258/abstract?rss=yes</link><description>For carcinoma specimens with non-grossly identifiable lesions such as microcalcifications, difficulties may be encountered in locating these abnormalities and sampling the margins that are at risk. This is magnified in the case of skin-sparing procedures where the margin is a much greater surface area and is the operation of choice in patients with diffuse microcalcifications and/or multifocal in situ disease. The objective of this study was to determine the efficacy of specimen radiographs of mastectomy in identifying occult carcinoma associated with microcalcifications and assessing the resection margins. We reviewed the histology and corresponding specimen radiographs of 16 patients with diffuse and widespread microcalcifications and who underwent skin-sparing mastectomy. After the specimens were serially sectioned, specimen radiographs of each section of the specimens were obtained with digital mammography equipment. Findings in the specimen radiographs were used to direct the histologic sampling of the specimens. On gross examination, two (12.5%) mastectomy specimens had identifiable discreet masses; the lesions were 4 and 7 mm, respectively. Histologic examination revealed the presence of carcinoma in 13 (81%) cases; seven with both infiltrating and in situ carcinoma and six with in situ carcinoma alone. The remaining three patients demonstrated only changes of biopsy site without any residual carcinoma. Microcalcifications were associated with in situ carcinoma in all malignant cases. Among the 12 cases with microcalcifications present at or within 2 mm of the margins, in situ carcinoma was present at the margins in three cases and located within 2 mm of the margins in two cases. All margins were negative in all cases with microcalcifications that were at least 1 cm away from the resection margins. The average number of tissue blocks examined was 16.6±5.4. The average number of tissue blocks sampled among randomly selected mastectomy specimens was 15.2±5.4. There was no statistically significant difference in the number of blocks between mastectomy cases with specimen radiographs taken and those without (t-test). Our study suggests that specimen radiographs may assist in identifying occult breast carcinoma associated with microcalcifications and assessing the resection margins without increased sampling.</description><dc:title>Specimen radiographs assist in identifying and assessing resection margins of occult breast carcinomas</dc:title><dc:creator>E.S. Young, D.H. Hogg, H. Krontiras, W. Bernreuter, M. Urist, K.I. Bland, D.C. Chhieng</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.009</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>160</prism:startingPage><prism:endingPage>160</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS089970710900326X/abstract?rss=yes"><title>Assessment of regional left ventricular function by dual source computed tomography: interobserver variability and validation to laevocardiography</title><link>http://www.clinicalimaging.org/article/PIIS089970710900326X/abstract?rss=yes</link><description>Assessment of left ventricular function is possible in contrast-enhanced cardiac CT data sets. However, rapid ventricular motion especially in systole can lead to artifacts. Dual source computed tomography (DSCT) has high temporal resolution which effectively limits motion artifact. We therefore assessed the accuracy of DSCT to detect regional left ventricular wall motion abnormalities in comparison to invasive cine angiocardiography.</description><dc:title>Assessment of regional left ventricular function by dual source computed tomography: interobserver variability and validation to laevocardiography</dc:title><dc:creator>T. Pflederer, K.T. Ho, T. Anger, R. Krahner, G. Muschiol, A. Renz, W.G. Daniel, S. Achenbach</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.010</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>160</prism:startingPage><prism:endingPage>161</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003271/abstract?rss=yes"><title>Quantitative assessment of left ventricular systolic wall thickening using multidetector computed tomography</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003271/abstract?rss=yes</link><description>Multidetector computed tomography (MDCT) of the heart provides both anatomical and functional information. The objective of this study was to evaluate the accuracy of quantitative assessment of left ventricular contractile function in relation to two-dimensional transthoracic echocardiography (TTE).</description><dc:title>Quantitative assessment of left ventricular systolic wall thickening using multidetector computed tomography</dc:title><dc:creator>T.S. Kristensen, K.F. Kofoed, D.V. Møller, M. Ersbøll, T. Kühl, P. von der Recke, L. Køber, M.B. Nielsen, H. Kelbæk</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.011</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>161</prism:startingPage><prism:endingPage>161</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003283/abstract?rss=yes"><title>Comparison of 64 MDCT coronary CTA and coronary angiography in the detection of coronary artery stenosis in low risk patients with stable angina and acute coronary syndrome [in French]</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003283/abstract?rss=yes</link><description>To determine the accuracy of 64 MDCT coronary CTA (CCTA) compared to coronary angiography in low-risk patients with stable angina and acute coronary syndrome and determine the number of significant coronary artery stenoses (&gt;50%) in these patients.</description><dc:title>Comparison of 64 MDCT coronary CTA and coronary angiography in the detection of coronary artery stenosis in low risk patients with stable angina and acute coronary syndrome [in French]</dc:title><dc:creator>G. Cazalas, A. Sarran, N. Amabile, K. Chaumoitre, S. Marciano-Chagnaud, A. Jacquier, F. Paganelli, M. Panuel</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.012</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>161</prism:startingPage><prism:endingPage>161</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003295/abstract?rss=yes"><title>Juxtapapillary duodenal diverticula: MDCT findings in 1010 patients and proposal of a new classification</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003295/abstract?rss=yes</link><description>The aim of this study is to analyze the MDCT findings of juxtapapillary duodenal diverticula (JPDD) and to propose a new radiological classification.   CT-examinations of 1010 consecutive patients, all examined by 16-row MDCT of the abdomen over a time period of 20 months were retrospectively analyzed. All study patients were examined by triple phase CT (native, arterial and portal venous CT scan) of the abdomen and all received positive oral contrast prior to the examination. Thirty-three patients showed a juxtapapillary duodenal diverticulum, which could be seen on all CT scans, but usually was depicted most clearly on the thin collimated arterial phase CT images. Size of diverticula range from 4 mm to 4.5 cm (mean 1.7 cm). In 17 cases the diverticulum was located ventrally to the vaterian sphincter complex, extending less or more into the pancreas at the site where the dorsal and the ventral anlage of the pancreas have fused (type I). 12 diverticula were located dorsally to the sphincter complex (type II).Three patients presented with a bilobated juxtapapillary diverticulum extending to both sides, ventrally and dorsally (type III) and one patient showed a little diverticulum ventrally to the minor papilla (type IV).Three patients presented with food impaction in the diverticulum but only one of these patients with a large IPDD showed a Lemmel-syndrome, whereas the other three patients with non-calculous extrahepatic cholostasis showed larger diverticula without food impaction. MDCT allows to identify four different types of juxtapapillary duodenal diverticula and using the proposed classification may be helpful for a more exact, anatomy based radiological description of this CT finding.</description><dc:title>Juxtapapillary duodenal diverticula: MDCT findings in 1010 patients and proposal of a new classification</dc:title><dc:creator>W. Wiesner, Ch. Beglinger, D. Oertli, W. Steinbrich</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.013</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>161</prism:startingPage><prism:endingPage>161</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003301/abstract?rss=yes"><title>Color Doppler sonography of small bowel wall changes in 21 consecutive cases of acute mesenteric ischemia</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003301/abstract?rss=yes</link><description>To describe the small bowel wall changes observed with color Doppler sonography in acute mesenteric ischemia with comparison with its outcome.   We reviewed the sonographic findings of 21 patients with a final diagnosis of acute mesenteric ischemia (12 acute arterial forms and 9 acute venous forms). These examinations included identification of non peristaltic thin-walled fluid-filled intestinal loops (with or without pneumatosis), thickened intestinal wall (&gt;3 mm) (noted as stratified or not), and preserved or absent mural flow assessed with color Doppler. Sonographic findings were compared with the surgical data (n=16) or with the clinical outcome (n=5).</description><dc:title>Color Doppler sonography of small bowel wall changes in 21 consecutive cases of acute mesenteric ischemia</dc:title><dc:creator>E.M. Danse, A. Kartheuser, H.M. Paterson, P.-F. Laterre</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.014</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>161</prism:startingPage><prism:endingPage>162</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003313/abstract?rss=yes"><title>Liver capsule retraction adjacent to a circumscribed liver lesion: review of 26 cases with histological confirmation [in French]</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003313/abstract?rss=yes</link><description>To review the histological features of 26 circumscribed liver lesions associated with liver capsule retraction ad discuss the differential diagnosis while evaluating for the presence of fibrous stromal reaction.</description><dc:title>Liver capsule retraction adjacent to a circumscribed liver lesion: review of 26 cases with histological confirmation [in French]</dc:title><dc:creator>D. Da Ines, V. Petitcolin, V. Lannareix, P.F. Montoriol, J. Joubert Zakeyh</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.015</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>162</prism:startingPage><prism:endingPage>162</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003325/abstract?rss=yes"><title>Transarterial ethanol ablation for sporadic and non-hemorrhaging angiomyolipoma of the kidney</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003325/abstract?rss=yes</link><description>We evaluated the efficacy and side effects of transarterial ethanol ablation in sporadic and non-hemorrhaging angiomyolipomas (AMLs) in the kidney.   A total of 10 patients with solitary and sporadic AMLs underwent selective transarterial absolute ethanol ablation for prophylaxis against hemorrhage. We confirmed the ratio areas of tumor vessel on angiogram, those of infraction on post-ablation computed tomography (CT) and those of tumor reduction in a 3-, 6- and 12-month follow-up CT.</description><dc:title>Transarterial ethanol ablation for sporadic and non-hemorrhaging angiomyolipoma of the kidney</dc:title><dc:creator>S. Takebayashi, A. Horikawa, M. Aral, S. Iso, K. Noguchi</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.016</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>162</prism:startingPage><prism:endingPage>162</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003337/abstract?rss=yes"><title>Differentiation of osteoporotic and neoplastic vertebral fractures by chemical shift [in-phase and out-of phase] MR imaging</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003337/abstract?rss=yes</link><description>The objective of this study was to establish the cut-off value of the signal intensity drop on chemical shift magnetic resonance imaging (MRI) with appropriate sensitivity and specificity to differentiate osteoporotic from neoplastic wedging of the spine.</description><dc:title>Differentiation of osteoporotic and neoplastic vertebral fractures by chemical shift [in-phase and out-of phase] MR imaging</dc:title><dc:creator>Y. Ragab, Y. Emad, T. Gheita, M. Mansour, A. Abou-Zeid, S. Ferrari, J.J. Rasker</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.017</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>162</prism:startingPage><prism:endingPage>162</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003349/abstract?rss=yes"><title>Imaging patterns in elastofibroma dorsi</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003349/abstract?rss=yes</link><description>Elastofibroma dorsi is a rare pseudotumor of the soft tissues. Its clinicoradiologic characteristics lead to a correct diagnosis.   We followed 43 patients with elastofibroma dorsi with a confirmed histological diagnosis or on the basis of typical imaging pattern (ultrasound, CT, MR) confirmed by evolution.</description><dc:title>Imaging patterns in elastofibroma dorsi</dc:title><dc:creator>M. Battaglia, D. Vanel, P. Pollasarri, A. Balladelli, M. Alberghini, E.L. Staals, C. Monti, S. Galletti</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.018</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>162</prism:startingPage><prism:endingPage>162</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003350/abstract?rss=yes"><title>Infantile fibrosarcoma: magnetic resonance imaging findings in six cases</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003350/abstract?rss=yes</link><description>To retrospectively review magnetic resonance (MR) imaging features in a series of six infantile fibrosarcomas to find out if MR can suggest this unusual diagnosis and to highlight the value of MR during and following treatment.</description><dc:title>Infantile fibrosarcoma: magnetic resonance imaging findings in six cases</dc:title><dc:creator>S. Canale, D. Vanel, D. Couanet, C. Patte, C. Caramella, C. Dromain</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.019</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>163</prism:startingPage><prism:endingPage>163</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003362/abstract?rss=yes"><title>Radiocontrast media associated exanthema: identification of cross-rentification of cross-reactivity and tolerability by allergologic testing</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003362/abstract?rss=yes</link><description>All iodinated radiocontrast media (RCM) may cause hypersensitivity reactions, either immediate-type within 5–10 min of RCM injection or delayed-type, which become apparent more than 1 h after RCM exposure. Delayed-type hypersensitivity to RCM may pose a problem for future radiologic investigations because due to possible immunological cross-reactivity all iodinated RCM are usually avoided.</description><dc:title>Radiocontrast media associated exanthema: identification of cross-rentification of cross-reactivity and tolerability by allergologic testing</dc:title><dc:creator>C.S. Seitz, P. Pfeuffer, P. Raith, E.-B. Bröcker, A. Trautmann</dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.020</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-03-01</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-03-01</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section>Abstracts</prism:section><prism:startingPage>163</prism:startingPage><prism:endingPage>163</prism:endingPage></item><item rdf:about="http://www.clinicalimaging.org/article/PIIS0899707109003374/abstract?rss=yes"><title>Meetings and courses</title><link>http://www.clinicalimaging.org/article/PIIS0899707109003374/abstract?rss=yes</link><description></description><dc:title>Meetings and courses</dc:title><dc:creator></dc:creator><dc:identifier>10.1016/j.clinimag.2009.12.021</dc:identifier><dc:source>Clinical Imaging 34, 2 (2010)</dc:source><dc:date>2010-01-25</dc:date><prism:publicationName>Clinical Imaging</prism:publicationName><prism:publicationDate>2010-01-25</prism:publicationDate><prism:volume>34</prism:volume><prism:number>2</prism:number><prism:issueIdentifier>S0899-7071(10)X0002-X</prism:issueIdentifier><prism:section></prism:section><prism:startingPage>164</prism:startingPage><prism:endingPage>164</prism:endingPage></item></rdf:RDF>