Intraepidermal Cells of Paget's Carcinoma of the Breast Can Be Genetically Different from Those of the Underlying Carcinoma

Luca Morandi, Annalisa Pession, Gian Luca Marucci, Maria Pia Foschini, Giancarlo Pruneri, Giuseppe Viale, Vincenzo Eusebi

Research output: Contribution to journalArticle

Abstract

Paget's carcinoma (PC) of the breast is characterized by neoplastic cells of "glandular" type located within the epidermis of the nipple-areolar complex, often associated with an underlying ductal carcinoma, either in situ or invasive. At present the origin of PC cells is controversial, although there is a widespread opinion that PC cells are "foreign" elements to the epidermis resulting from an epidermotropic migration of neoplastic elements from an underlying ductal carcinoma. An alternative view is that some cases result from neoplastic transformation of preexisting, innocent intraepidermal clear cells of the nipple-areolar complex (Toker cells) that migrate from nonneoplastic ducts. Consequently, 10 cases were studied using methods for clonality (ie, loss of heterozygosity and mitochondrial DNA displacement loop sequence analysis). Microdissection of intraepidermal neoplastic cells and of cells from underlying duct carcinomas and metastases was performed. In no fewer than 2 cases, PC cells were genetically different from underlying lesions, which showed consistent homology among themselves. Therefore, it is suggested that the rtde of epidermotropism by neoplastic cells from an underlying carcinoma is not applicable to all cases, and that in some cases PC cells might be the result of neoplastic transformation of preexisting intraepidermal nonneoplastic cells. Consequently, the underlying tumors are coincidental neoplastic lesions (collision tumors).

Original languageEnglish
Pages (from-to)1321-1330
Number of pages10
JournalHuman Pathology
Volume34
Issue number12
DOIs
Publication statusPublished - Dec 2003

Keywords

  • Breast
  • Clonality
  • Displacement loop
  • Loss of heterozygosity
  • Paget's carcinoma

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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