Abstract
Objectives: (1) To assess the statistical correlation between the tumor thickness (TT) by ultrasonography
(USG) and microscopic measurement in cases of early oral tongue squamous cell carcinoma
(OTSCC). (2) To assess the predictive capacity of TT by ultrasound in detecting nodal
metastasis. Materials and Methods: Prospective analysis was performed in 24 patients for a period of 2 years from 2012
to 2013. Nodal status and TT measurement was done preoperatively by neck and intraoral
USG respectively in cases of early (pT1 & T2, clinically N0) OTSCC. As per the institution
protocol after histopathological confirmation of malignancy, all patients underwent
resection of primary lesion and ipsilateral elective neck dissection (Level - I to
IV). Measurement of TT was obtained intraoperatively from fresh glossectomy specimen
and postoperatively from histopathological paraffin section examination. The statistical
correlation between TT measured by USG and histopathology was assessed by Pearson’s
correlation coefficient. Chi-square test was used to find the association of pathological
T stage, TT with pathological nodal status. Results: Significant statistical correlation was seen between TT by USG and microscopic measures.
Between the two, TT measurements were within 1 mm in 37.5% (9/24) of cases, within
2 mm in 29.16% (7/24), and was greater than 2 mm in 8 cases. The Pearson’s correlation
r is 0.678 (P < 0.001) and ICC (interclass correlation coefficient) is 0.808. The average difference
between microscopic and US thickness (Bias) is -0.14637 and the limits of agreement
is (4.717, -4.863) with 95% limits of agreement. The rate of occult nodal metastasis
was 16.6% and TT of <4 mm had no incidence of nodal metastasis. Conclusion: Ultrasonographic evaluation is reliable and cost-effective tool to measure the TT
preoperatively, which will be of help in deciding the management in early OTSCC. TT
of 4 mm and above was predictor of occult cervical nodal metastasis.
Keywords
Ultrasound tongue - oral tongue cancer - squamous cell cancer