Characteristic MR Signal of Velopharyngeal-Related Muscles on Cine-MRI in Patients with Oral Cancers and Preserved Swallowing Function: An Exploratory Feasibility Study
Year: 2026
Type: article
Study design: Observational Study
Abstract: BACKGROUND/OBJECTIVES: Surgically treated oral cancer patients often face velopharyngeal insufficiency, which adversely impacts their quality of life (QOL). Our past investigations revealed noticeable MR signal shifts in velopharyngeal-related muscles during water deglutition on CMR among healthy individuals. We hypothesized that analyzing these distinct signal fluctuations could offer a novel visual perspective for detecting deglutition anomalies in surgical oral cancer cases. This feasibility study aimed to assess velopharyngeal-related muscular performance via CMR in post-operative oral cancer patients. METHODS: Nineteen patients with oral malignancies were prospectively evaluated pre- and post-operatively. Twelve quantitative CMR metrics alongside subjective dysphagia scores were investigated. We analyzed whether signal intensity (SI) ratio alterations in these muscles correlated with dysphagia severity and clinical parameters. RESULTS: Although three specific CMR parameters significantly worsened post-operatively, muscle MR signal values increased during deglutition without significant variation between pre- and post-surgical states. Subjective swallowing assessments remained entirely normal across all subjects. CONCLUSIONS: This preliminary investigation indicates that CMR can visualize stable velopharyngeal-related muscle activity after surgery in oral cancer patients maintaining adequate swallowing status. Nevertheless, confirmation via larger, symptomatic patient cohorts alongside gold-standard techniques remains mandatory.
Source: Tomography
Institutions: Kyushu Dental University, Fukuoka Dental College
Language: English
Subfield: Speech and Hearing
Field: Health Professions
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,896
OpenAlex ID: W7203822217
