Columnar cell lesions of the breast: The missing link in breast cancer progression? A morphological and molecular analysis


Autoria(s): Simpson, P. T.; Gale, T.; Reis-Filho, J. S.; Jones, C.; Parry, S.; Sloane, J. P.; Hanby, A.; Pinder, S. E.; Lee, A. H. S.; Humphreys, S.; Ellis, I. O.; Lakhani, S. R.
Contribuinte(s)

S. E. Mills

Data(s)

01/06/2005

Resumo

Columnar cell lesions (CCLs) of the breast are a spectrum of lesions that have posed difficulties to pathologists for many years, prompting discussion concerning their biologic and clinical significance. We present a study of CCL in context with hyperplasia of usual type (HUT) and the more advanced lesions ductal carcinoma in situ (DCIS) and invasive ductal carcinoma. A total of 81 lesions from 18 patients were subjected to a comprehensive morphologic review based upon a modified version of Schnitt's classification system for CCL, immunophenotypic analysis (estrogen receptor [ER], progesterone receptor [PgR], Her2/neu, cytokeratin 5/6 [CK5/6], cytokeratin 14 [CK14], E-cadherin, p53) and for the first time, a whole genome molecular analysis by comparative genomic hybridization. Multiple CCLs from 3 patients were studied in particular detail, with topographic information and/or showing a morphologic spectrum of CCL within individual terminal duct lobular units. CCLs were ER an PgR positive, CK5/6 and CK14 negative, exhibit low numbers of genetic alterations and recurrent 16q loss, features that are similar to those of low grade in situ and invasive carcinoma. The molecular genetic profiles closely reflect the degree of proliferation and atypia in CCL, indicating some of these lesions represent both a morphologic and molecular continuum. In addition, overlapping chromosomal alterations between CCL and more advanced lesions within individual terminal duct lobular units suggest a commonality in molecular evolution. These data further support the hypothesis that CCLs are a nonobligate, intermediary step in the development of some forms of low grade in situ and invasive carcinoma. Copyright: © 2005 Lippincott Williams & Wilkins, Inc.

Identificador

http://espace.library.uq.edu.au/view/UQ:74733

Idioma(s)

eng

Publicador

Lippincott Williams & Wilkins

Palavras-Chave #Pathology #Surgery #Breast Cancer #Columnar Cell Lesions #Comparative Genomic Hybridization #Precursor Lesion #Carcinoma In-situ #Standard Reference Intervals #Tubular Carcinoma #Genetic Pathways #Hyperplasia #Diagnosis #Proliferations #Management #Disease #C1 #321020 Pathology #730108 Cancer and related disorders #110316 Pathology (excl. Oral Pathology) #1103 Clinical Sciences
Tipo

Journal Article