Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Objectives: The aim of this study was performed to investigate the apparent diffusion coefficient (ADC) for distinguishing between benign and malignant lesions in submandibular and sublingual spaces.
Methods: Thirteen patients with benign and malignant lesions in submandibular and sublingual spaces were evaluated by MRI. The MRI were obtained by a 1.5 T MR unit using a head coil, and included T1-weighted image (T1WI), T2-weighted image (T2WI) and diffusion-weighted image (DWI). The ADC maps were calculated automatically by the DWI obtained with b = 800 s/mm. We placed regions of interest (ROI) to measure the ADC values on ADC maps, and the ADC value were automatically analyzed. The ADC in benign and malignant lesions were compared by Mann-Whitney U test with a 5% significance level.
Results: Regarding all lesions, T1WI, T2WI and DWI showed low-, high- and high-signal intensity area, respectively. The ADC of malignant lesions (1.10 ± 0.05 × 10 mms) was lower than those of benign lesions (2.36 ± 0.64 × 10 mms, p = 0.001).
Conclusion: The ADC could be effective for the objectively and quantitatively diagnosis of submandibular and sublingual malignant tumors.
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http://dx.doi.org/10.1007/s11282-025-00857-8 | DOI Listing |