Perineural invasion is a feature associated with significantly poorer outcomes when present in cutaneous squamous cell carcinoma (CSCC). The incidence of this subset of CSCC continues to rise in the US, as does the confusion surrounding exactly how it should be managed. While management typically in
Neural cell adhesion molecule expression: No correlation with perineural invasion in cutaneous squamous cell carcinoma of the head and neck
β Scribed by C. Arturo Solares; Ian Brown; Glen M. Boyle; Peter G. Parsons; Benedict Panizza
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 238 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Background.
Perineural invasion (PNI) in cutaneous squamous cell carcinoma of the head and neck (CSCCHN) is associated with decreased survival, particularly in patients with clinical signs of cranial nerve involvement. There is evidence to indicate that neural cell adhesion molecule (NβCAM) confers capability of PNI. We analyzed our own patient population to determine if NβCAM predicted clinical PNI in CSCCHN.
Methods.
Tissue from patients with CSCCHN and clinical PNI, who underwent surgery between 1998 and 2005, was immunostained for NβCAM. In addition, nonβPNI CSCCHN and normal nerve sections were also stained. A section of neuroendocrine tumor was included in each slide as a positive control. In addition, most of the sections also had an βinbuilt controlβ in the CD56 positive natural killer T cells that formed part of the inflammatory reaction to the tumors.
Results.
Tissue was available from 14 patients with CSCCHN and clinical PNI. The analysis was carried out in 14 patients without PNI and 4 normal nerves. NβCAM was not expressed in any of our PNI CSCCHN specimens or nonβPNI controls. It was strongly expressed in the neuroendocrine tumors and positive inβbuilt controls, as well as in normal nerve tissue.
Conclusion.
NβCAM expression did not predict neurotropism in our patient population. Additional studies are required to identify the cell surface markers expressed by CSCCHN which confer neurotropism capabilities. Β© 2009 Wiley Periodicals, Inc. Head Neck, 2009
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