CT findings of mild forms or early manifestations of acute cholecystitis
Abstract Objective The objective of this study was to determine the most predictive CT feature of the mild forms or early manifestations of acute cholecystitis. Materials and Methods Two radiologists analyzed CT of 34 patients with mild or early acute cholecystitis and 34 control patients for perich...
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Published in: | Clinical imaging Vol. 33; no. 4; pp. 274 - 280 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New York, NY
Elsevier Inc
01-07-2009
Elsevier Elsevier Limited |
Subjects: | |
Online Access: | Get full text |
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Summary: | Abstract Objective The objective of this study was to determine the most predictive CT feature of the mild forms or early manifestations of acute cholecystitis. Materials and Methods Two radiologists analyzed CT of 34 patients with mild or early acute cholecystitis and 34 control patients for pericholecystic increased attenuation on the arterial phase, indistinctness of the interface between the gallbladder (GB) and the liver, enhancement of the GB wall, and increased attenuation of the GB bile. Results There were significant differences in the mean values for each CT feature but increased attenuation of the GB bile between patients and control group ( P <.05). The most significant predictor of mild or early acute cholecystitis on CT was the presence of pericholecystic increased attenuation on the arterial phase (sensitivity, 82.4%), followed by indistinctness of the interface between the GB and liver (sensitivity, 38.0%), which were identified by both observers with good agreement ( κ =0.735 and κ =0.687). Conclusions The pericholecystic increased attenuation on arterial phase CT was the most significant predictor of mild forms or early manifestations of acute cholecystitis. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0899-7071 1873-4499 |
DOI: | 10.1016/j.clinimag.2008.11.004 |