Myoepithelial Cell Markers in Salivary Gland Neoplasms

Author:

Furuse Cristiane1,de Sousa Suzana O. Machado,Nunes Fabio Daumas,de Magalhaes Marina Helena Cury Gallottini2,de Arauijo Vera Cavalcanti3

Affiliation:

1. Department of Oral Pathology, Sao Leopoldo Mandic Dental Research Institute, Campinas

2. Department of Oral Pathology, School of Dentistry, University of Sao Paulo, Sao Paulo, Brazil.

3. Department of Oral Pathology, Sao Leopoldo Mandic Dental Research Institute, Campinas; Disciplina de Patologia Bucal, Faculdade de Odontologia USP, Av. Prof. Lineu Prestes, 2227, 05508-900, Sao Paulo-SP, Brazil.

Abstract

We compared the immunoexpression of 5 myoepithelial cell (MEC) markers (asmooth-muscle actin, calponin, h-caldesmon, vimentin, and S-100-protein) using 16 pleomorphic adenomas (PA), 15 adenoid cystic carcinomas (ACC), and 3 epithelialmyoepithelial carcinomas (EMC) of salivary glands. The cx-smooth-muscle actin was useful for identification of MECs, especially in cribriform and tubular ACC, followed by EMC. Calponin was similar to ct-smooth-muscle actin, except for polygonal and plasmacytoid cells of PA and for solid ACC, which showed a-smooth-muscle actin negative and calponin positive. H-caldesmon was negative. Vimentin immunostained all MEC types, and was negative in luminal cells. S-100 protein was expressed both in the nuclei and cytoplasm of MECs and luminal cells, especially in PA. The best way to identify MEC is using a-smooth-muscle actin or calponin, plus vimentin, since in tumors MECs are hardly ever fully differentiated.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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