Reconceiving Perineural Invasion in Cutaneous Squamous Cell Carcinoma: From Biological to Histopathological Assessment

Pathobiology. 2024;91(6):442-454. doi: 10.1159/000539484. Epub 2024 Jul 24.

Abstract

Background: Perineural invasion (PNI) is a complex molecular process histologically represented by the presence of tumor cells within the peripheral nerve sheath and defined when infiltration into the 3 nerve sheath layers can be clearly identified. Several molecular pathways have been implicated in cSCC. PNI is a well-recognized risk factor in cutaneous squamous cell carcinoma (cSCC) and its accurate assessment represents a challenging field in pathology daily practice.

Summary: As a highly intricate and dynamic process, PNI involves a contingent on bidirectional signaling interactions between the tumor and various nerve components, such as Schwann cells and neurons. The current staging systems recommend the identification of PNI as a dichotomous variable (presence vs. absence) to identify a subgroup of high-risk patients. However, recent further insights revealed that the evaluation of morphological PNI-related features in cSCC may enhance the prognostic stratification of patients and may optimize the current staging guidelines for recurrence risk assessment and improvement of patient selection for postoperative adjuvant treatments. Furthermore, recent emerging biomarkers could redefine early PNI detection.

Key messages: This review provides updated insights into cSCC with PNI, focusing on molecular and cellular pathogenic processes, and aims to increase knowledge on prognostic relevant PNI-related histological features.

Keywords: Cellular mechanisms; Cutaneous squamous cell carcinoma; Histopathology; Incidental PNI; Perineural invasion.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor / metabolism
  • Carcinoma, Squamous Cell* / pathology
  • Humans
  • Neoplasm Invasiveness*
  • Peripheral Nerves / pathology
  • Prognosis
  • Skin Neoplasms* / pathology

Substances

  • Biomarkers, Tumor

Grants and funding

This study was supported by grants from Associazione Italiana per la Ricerca sul Cancro (AIRC) under IG 2020 - ID 24503 (RN).