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Sialoblastoma: A case report and review of the literature on congenital epithelial tumors of salivary Gland origin

  • Chuen Hsueh
  • , F. Gonzalez-Crussi*
  • *Corresponding author for this work
  • Northwestern University

Research output: Contribution to journalJournal Article peer-review

46 Scopus citations

Abstract

The histologic, immunohistochemical, and ultrastructural features of a congenital epithelial tumor of the parotid were studied. The tumor was characterized by solid nests of epithelial cells intermingled with proliferating ductal structures lined by a double layer of cells. Immunoperoxidase staining for cytokeratin, vimentin, actin, and S-100 protein showed the presence of cytokeratin in the ductal cells as well as the presence of vimentin, actin, and S-100 protein in the outermost layer of the ducts. The solid nests were focally reactive to S-100 and vimentin. Ultrastructural examination revealed myoepithelial cells with replication of basement membrane material. The tumor recurred 17 months after excision without lymph node involvement or metastasis. The term "sialoblastoma" is favored. Review of the literature on congenital, epithelial salivary gland tumors showed that a few cases recurred locally and only one case had regional lymph node involvement. No distant metastasis has been reported..

Original languageEnglish
Pages (from-to)205-214
Number of pages10
JournalFetal and Pediatric Pathology
Volume12
Issue number2
DOIs
StatePublished - 1992
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Basal cell adenoma
  • Congenital tumor
  • Parotid gland
  • Salivary gland

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