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J Clin Pathol 2005;58:1311-1314 doi:10.1136/jcp.2004.025205
  • Original article

Maspin expression in carcinoma ex pleomorphic adenoma

  1. M T Martins1,
  2. A Altemani2,
  3. L Freitas2,
  4. V C Araújo3
  1. 1Department of Oral Pathology, School of Dentistry, University of São Paulo, 05508-900, São Paulo, SP, Brazil
  2. 2Department of Pathology, School of Medicine, University of Campinas, 13083-970 Campinas, SP, Brazil
  3. 3São Leopoldo Mandic Centre, 13041-445 Campinas, SP, Brazil
  1. Correspondence to:
    Dr M T Martins
    Department of Oral Pathology, School of Dentistry, University of São Paulo, Avenue Prof. Lineu Prestes, 2227, 05508-900, São Paulo, SP, Brazil; mariliamusp.br
  • Accepted 30 March 2005

Abstract

Aims: To investigate the presence and distribution of the protein maspin in carcinoma ex pleomorphic adenoma (CXPA).

Methods: Maspin expression was studied by means of immunohistochemistry in 16 cases of CXPA, using the labelled polymer method.

Results: According to the extent of invasion, the tumours were subdivided into: intracapsular (five cases), minimally invasive (four cases), and invasive (seven cases). Twelve patients had carcinoma with only epithelial differentiation, whereas four had a malignant myoepithelial component. Non-luminal cells in the duct-like structures of the remnant pleomorphic adenoma were strongly positive for maspin, whereas only a few luminal cells were immunopositive. A few positive cells were seen in the frequent hypocellular and hyalinised areas. Maspin was abundantly expressed, mainly in non-luminal cells, in transitional areas of CXPA with only epithelial differentiation. In frankly carcinomatous areas there was a gradual decrease in maspin expression. Almost all cells were maspin positive in CXPA with a myoepithelial component. When present, luminal cells were in general negative for maspin.

Conclusions: When only epithelial cells undergo malignant transformation, maspin expression is gradually lost. In cases with a myoepithelial component, maspin expression is high, and this might be related to the tumour suppressor activity attributed to this cell.

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