Breast Cancer with Neoductgenesis: Histopathological Criteria and Its Correlation with Mammographic and Tumour Features

Author:

Zhou Wenjing1ORCID,Sollie Thomas2,Tot Tibor3ORCID,Pinder Sarah E.4,Amini Rose-Marie5,Blomqvist Carl6,Fjällskog Marie-Louise7,Christensson Gunilla8,Abdsaleh Shahin7,Wärnberg Fredrik19

Affiliation:

1. Department of Surgical Sciences, Uppsala University, 751 85 Uppsala, Sweden

2. Department of Pathology, Örebro University, 701 85 Örebro, Sweden

3. Department of Pathology, Falun Central Hospital, 791 82 Falun, Sweden

4. Department of Research Oncology, King’s College London, London SE1 9RT, UK

5. Department of Immunology, Genetics and Pathology, Uppsala University, 751 85 Uppsala, Sweden

6. Department of Oncology, Helsinki University Central Hospital, 00029 Helsinki, Finland

7. Department of Radiology, Oncology and Radiation Science, Uppsala University, 751 85 Uppsala, Sweden

8. Department of Surgery, Falun Central Hospital, 791 82 Falun, Sweden

9. Department of Surgery, Uppsala Academic Hospital, 751 85 Uppsala, Sweden

Abstract

Introduction. Breast cancer with mammographic casting type calcifications, high grade DCIS with an abnormal number of ducts, periductal desmoplastic reaction, lymphocyte infiltration, and tenascin-C (TN-C) overexpression has been proposed to represent a more aggressive form of breast cancer and has been denominated as breast cancer with neoductgenesis. We developed histopathological criteria for neoductgenesis in order to study reproducibility and correlation with other tumour markers.Methods. 74 cases of grades 2 and 3 DCIS, with or without an invasive component, were selected. A combined score of the degree(s) of concentration of ducts, lymphocyte infiltration, and periductal fibrosis was used to classify cases as showing neoductgenesis, or not. Diagnostic reproducibility, correlation with tumour markers, and mammographic features were studied.Results. Twenty-three of 74 cases were diagnosed with neoductgenesis. The kappa value between pathologists showed moderate reproducibility (0.50) (95% CI; 0.41–0.60). Neoductgenesis correlated significantly with malignant type microcalcifications and TN-C expression (P=0.008and 0.04) and with ER, PR, and HER2 status (P<0.00001for all three markers).Conclusions. We developed histological criteria for breast cancer with neoductgenesis. Neoductgenesis, by our applied histopathological definition was related to more aggressive tumour biology and malignant mammographic calcifications.

Publisher

Hindawi Limited

Subject

Cancer Research,Pharmacology (medical),Oncology

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