Prognostic Significance of Peritumoral and Intratumoral Lymphatic Vessels Density in Clinically Node-Negative (cN0) Oral Squamous Cell Carcinoma: A Preliminary Report

<i>Background and Objectives</i>: Oral squamous cell carcinoma (OSCC) is characterized by a high propensity for cervical lymph node metastasis, which remains a strong predictor of patient outcome. Despite advances in management, the prognosis for OSCC has not significantly improved, and the identification of reliable predictors for occult lymph node metastasis (OLNM) in clinically node-negative (cN0) patients is crucial for optimizing treatment strategies. Lymphovascular density (LVD) immunohistochemically assessed by podoplanin (D2-40) has been proposed as a potential biomarker for regional metastasis, but its prognostic value remains controversial. This study aimed to evaluate the prognostic significance of intratumoral (ILVD) and peritumoral lymphovascular density (PLVD) for OLNM in OSCC. <i>Materials and Methods</i>: A retrospective analysis was conducted on 43 cN0 patients with primary OSCC who underwent surgical resection and elective neck dissection (END) at a tertiary care cancer center. LVD was assessed by immunohistochemical staining for podoplanin (D2-40) in both intratumoral and peritumoral regions. Clinicopathological data were collected and statistically analyzed. <i>Results</i>: In observed cohort peritumoral LVD was significantly higher than intratumoral LVD. PLVD was also significantly higher in early-stage tumors (pT1/pT2) compared to advanced stages (pT3/pT4). Higher ILVD was significantly associated with the presence of OLNM. Neither ILVD nor PLVD demonstrated a statistically significant influence on overall survival, although a trend toward poorer outcomes was observed in patients with higher ILVD. <i>Conclusions</i>: ILVD was significantly associated with occult nodal metastasis, whereas PLVD was not. However, neither LVD parameter independently predicted overall survival. Results suggest that ILVD may serve as a useful marker for identifying cN0 OSCC patients at higher risk for occult metastasis.