Grading and Study of Biological Markers in Ductal Carcinoma in situ and Concurrent Infiltrating Ductal Carcinoma of Breast
Introduction: Breast cancer is the most common cancer in women. Breast cancer has surpassed cervical cancer and is now the leading cause of cancer death; however, cervical cancer still remains common in rural areas. Aim: To assess the architectural pattern, nuclear grade, presence and absence of nec...
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Veröffentlicht in: | Journal of clinical and diagnostic research 2018-04, Vol.12 (4), p.EC01-EC04 |
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Sprache: | eng |
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Zusammenfassung: | Introduction: Breast cancer is the most common cancer in women. Breast cancer has surpassed cervical cancer and is now the leading cause of cancer death; however, cervical cancer still remains common in rural areas. Aim: To assess the architectural pattern, nuclear grade, presence and absence of necrosis of Infiltrating Duct Carcinoma (IDC) and concurrent Ductal Carcinoma in situ (DCIS) and to correlate the biological markers of the two. Materials and Methods: The present study was carried out in the Department of Pathology, Father Muller Medical College, Mangaluru, Karnataka, India from January 2011 to February 2013. The mastectomy and lumpectomy specimens received in the histopathology laboratory were studied for the presence of IDC and concurrent DCIS. Haematoxylin and Eosin (H&E) staining for histological diagnosis and IHC analysis for ER, PR and Her-2/neu was carried out. All the data were analysed using SSPS software version 13.0. Results: This study included total 60 cases of IDC (NOS) with concurrent DCIS. The mean age of patients was 48.6 years (SD ±11.21). Most common anatomic location was in the left breast. Majority of tumours were Grade 2 followed by Grade 3. The grades of the IDC and coexisting DCIS were concordant in 66.66% cases and 33.33% cases showed discordance. Also, 98.33% of cases showed similar expression of ER, PR and Her2/ neu in both the components. Statistically, a strong correlation was seen in the grades, ER, PR and Her2/neu expression of IDC and DCIS (p |
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ISSN: | 2249-782X 0973-709X |
DOI: | 10.7860/JCDR/2018/29321.11422 |