Schneiderian Papillomas and Carcinomas: A Retrospective Study with Special Reference to p53 and p16 tumor suppressor gene expression and association with HPV

Author:

Cheung Florence M.F.1,Lau Tina W.S.1,Cheung Leslie K.N.1,Li Albert S.M.1,Chow Shun Kit2,Lo Anthony W.I.3

Affiliation:

1. From the Department of Clinical Pathology, Pamela Youde Nethersole Eastern Hospital, Hong Kong

2. Department of Ear, Nose & Throat, Pamela Youde Nethersole Eastern Hospital, Hong Kong

3. Department of Anatomical and Cellular Pathology, the Chinese University of Hong Kong.

Abstract

Schneiderian papillomas are uncommon benign tumors of the sinonasal area. They are prone to local aggressiveness and recurrence, and some undergo malignant progression. We analyzed specimens obtainedfrom 67 Chinese patients who had presented to the ENT department of a regional hospital with biopsy-proven schneiderian papilloma. Seven of these patients had either synchronous or metachronous carcinoma, 1 of whom had pure carcinoma in situ. For each case, we documentedthe morphology, immunohistochemical expression of tumor suppressor genes p53 and p16, and any association with human papillomavirus (HPV) infection as detected by either polymerase chain reaction or in situ hybridization techniques. We found that severe dysplasia andp53positivity were strongly associated with malignantprogression. Association with HPV was demonstrated in 22 of the 67patients (33%); the association was strongest among patients with exophytic papillomas and carcinomas. The effect of HPV in papilloma oncogenesis probably begins duringthe early phase, while other factors are responsible for progression to carcinoma. We conclude thatp53-positive, dysplastic schneiderian papillomas warrant aggressive surgical treatment.

Publisher

SAGE Publications

Subject

Otorhinolaryngology

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