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Differential diagnosis of pleomorphic adenoma by immunohistochemical means

Published online by Cambridge University Press:  29 June 2007

Toshiro Nishimura*
Affiliation:
Departments of Otolaryngology, School of Medicine, Kanazawa University
Mitsuru Furukawa
Affiliation:
Departments of Otolaryngology, School of Medicine, Kanazawa University
Ei Kawahara
Affiliation:
Departments of Pathology, School of Medicine, Kanazawa University
Atsuo Miwa
Affiliation:
Section of Pathology, Toyama Central Prefectural Hospital.
*
Toshiro Nishimura, M.D., Department of Otolaryngology, Suzu City General Hospital, lidamachi 5–9, Suzu 927–12, Ishikawa, Japan.

Abstract

Immunohistochemical study of major salivary gland tumours was performed on 60 pleomorphic adenomas, five basal cell adenomas and 10 adenoid cystic carcinomas to determine the diagnostic value of each antigen. Immunoreactivity examined were intermediate filaments (keratin, vimentin, desmin and glial fibrillary acidic protein [GFAP]) and related substances (actin, S-100 protein and secretory component). In pleomorphic adenomas, there was positive immunoreactivity for GFAP which was not observed in normal tissue or other neoplastic tissues. Immunoreactivity of GFAP was closely related to myxomatous and early chondromatous differentiation in pleomorphic adenoma. It is considered that GFAP immunoreactivity should be assessed in the occasional differential diagnostic dilemma of pleomorphic adenoma versus adenoid cystic carcinoma and basal cell adenoma, because of its ability to show potential and definite myxochondromatous differentiation.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 1991

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References

Anderson, C., Knibbs, R. D., Abbott, J. S., Pederson, C., Krutch koff, D. (1990) Glial fibrillary acidic protein expression in pleomorphic adenoma of salivary gland: an immunoelectron microscopic study. Ultrastructural Pathology, 14: 263271.CrossRefGoogle ScholarPubMed
Hsu, S., Raine, L., Fanger, H. (1981) Use of avidin-biotin-peroxidase complex (ABC) in immunohistochemical techniques: a comparison between ABC and unlabelled antibody (PAP) procedure. Journal of Histochemistry and Cytochemistry, 29: 577580.CrossRefGoogle Scholar
Moll, R., Franke, W. W., Schiller, L. D. (1982) The catalogue of human cytokeratins: patterns of expression in normal epithelia, tumours and cultured cells. Cell, 31: 1124.CrossRefGoogle ScholarPubMed
Nakazato, Y., Ishizeki, J., Takahashi, K., Yamaguchi, H., Kamei, T., Mori, T. (1982) Localization of S-100 protein and glial fibrillary acidic protein-related antigen in plomorphic adenoma of the salivary glands. Laboratory Investigations, 46: 621626.Google Scholar
Thackray, C. A., Lucas, B. R. (1974) Tumours of the major salivary glands, 1st ed., Armed Forces Institute of Pathology. Washington, D.C., p. 1639.Google Scholar
Thackray, C. A., Sobin, H. L. (1972) Histologic typing of salivary gland tumours. 1st ed., World Health Organization, Geneva, p. 2027.Google Scholar