Breast Pathology

Author:   Melinda Sanders, MD ,  Jean Simpson ,  David Elder
Publisher:   Demos Medical Publishing
ISBN:  

9781936287680


Pages:   328
Publication Date:   26 March 2014
Format:   Hardback
Availability:   Out of stock   Availability explained
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

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Breast Pathology


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Full Product Details

Author:   Melinda Sanders, MD ,  Jean Simpson ,  David Elder
Publisher:   Demos Medical Publishing
Imprint:   Demos Medical Publishing
Dimensions:   Width: 21.60cm , Height: 2.00cm , Length: 27.90cm
Weight:   1.281kg
ISBN:  

9781936287680


ISBN 10:   1936287684
Pages:   328
Publication Date:   26 March 2014
Audience:   College/higher education ,  Professional and scholarly ,  Postgraduate, Research & Scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   Out of stock   Availability explained
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

Table of Contents

"""1. Alterations of enlarged lobular units; 1.1 apocrine cyst versus columnar cell lesion without atypia; 1.2 columnar cell lesion with atypia versus columnar cell lesion without atypia; 1.3 secretory change versus columnar cell lesion with atypia ; 1.4 hypersecretory change versus ductal carcinoma in situ ; 1.5 papillary apocrine change versus apocrine ductal carcinoma in situ; 2. Epithelial proliferative lesions ; 2.1 Usual hyperplasia versus atypical ductal hyperplasia; 2.2 Gynecomastoid ñtype hyperplasia versus micropapillary atypical ductal hyperplasia or micropapillary ductal carcinoma in situ; 2.3 Usual hyperplasia (solid pattern) versus atypical ductal hyperplasia; 2.1 Prominent myoepithelial cells versus atypical ductal hyperplasia; 2.2 Papilloma involved by florid hyperplasia versus atypical ductal hyperplasia ; 2.3 Atypical ductal hyperplasia versus low grade ductal carcinoma in situ; 2.4 Cribriform atypical ductal hyperplasia versus collagenous spherulosis; 2.5 Atypical ductal hyperplasia versus atypical lobular hyperplasia; 2.6 Florid hyperplasia versus intermediate or high grade ductal carcinoma in situ; 2.7 Mucocele-like lesion with atypical ductal hyperplasia versus mucocele-like lesion without atypia; 2.8 Papillary apocrine change versus apocrine atypical ductal hyperplasia or apocrine ductal carcinoma in situ ; ; 3 Ductal carcinoma in situ; 3.1 Ductal carcinoma in situ versus atypical lobular hyperplasia in a papilloma; 3.2 Ductal carcinoma in situ versus microinvasive carcinoma; 3.3 Entrapped epithelial elements post biopsy of ductal carcinoma in situ in papilloma versus invasion; 3.4 Spindle cell pattern ductal carcinoma in situ versus florid hyperplasia; 3.5 Encysted noninvasive papillary carcinoma versus atypical ductal hyperplasia in a papilloma; 3.6 Pagetís disease versus toker cells; 3.7 Ductal carcinoma in situ versus lobular carcinoma in situ; 3.8 Secretory ductal carcinoma in situ versus usual hyperplasia with clear cells; 3.9 Pagetoid pattern ductal carcinoma in situ versus ALH; 3.10 Radiation change versus ductal carcinoma in situ; ; 4 Lobular carcinoma in situ; 4.1 Classic lobular carcinoma in situ versus variant lobular carcinoma in situ; 4.2 Classic lobular carcinoma in situ versus atypical lobular hyperplasia; 4.3 Usual hyperplasia with prominent myoepithelial cells versus lobular neoplasia; 4.4 Ductal involvement by cells of atypical lobular hyperplasia versus low grade ductal carcinoma in situ; ; 5 Sclerosing and adenotic lesions; 5.1 Nodular sclerosing adenosis versus papilloma; 5.2 Papilloma versus adenomyoepithelioma; 5.3 Radial scar versus pure tubular carcinoma; 5.4 Sclerosed adenotic papilloma versus tubular carcinoma; 5.5 Sclerosing adenosis versus microglandular adenosis; 5.6 Nonspecific perilobular or periductal chronic inflammation versus sclerosing lymphocytic lobulitis; ; 6 Fibroepithelial lesions; 6.1 Fibroadenoma versus cellular fibroadenoma; 6.2 Fibroadenoma versus benign phyllodes tumor; 6.3 Benign phyllodes tumor versus borderline phyllodes tumor; 6.4 Borderline phyllodes tumor versus malignant phyllodes tumor; 6.5 Malignant phyllodes tumor versus pure sarcoma ; ; 7 Stromal lesions; 7.1 Myofibroblastoma versus fibromatosis; 7.2 Epithelioid myofibroblastoma versus pure invasive lobular carcinoma; 7.3 Myofibroblastoma versus low grade spindle cell metaplastic carcinoma; 7.4 Spindle cell metaplastic carcinoma versus post biopsy spindle cell nodule; 7.5 Fibromatosis versus scar; ; 8 Special type carcinomas; 8.1 Invasive pure lobular carcinoma versus lobular variant carcinomas versus no special type carcinoma with lobular features ; 8.2 Pure nvasive cribriform carcinoma versus cribriform ductal carcinoma in situ ; 8.3 Invasive pure tubular carcinoma versus no special type carcinoma with tubular features ; 8.4 Pure mucinous carcinoma versus mucocele-like lesion; 8.5 Pure medullary carcinoma versus no special type carcinoma with medullary features; 8.6 Secretory carcinoma versus no special type carcinoma; 8.7 Adenoid cystic carcinoma versus no special type carcinoma with myoepithelial phenotype or ductal carcinoma in situ ; 8.8 Low grade spindle cell metaplastic carcinoma versus fibromatosis; 8.9 Adenosquamous carcinoma versus squamous metaplasia; 8.10 Histiocytes versus histiocytoid variant of invasive lobular carcinoma; 8.11 Atypical lobular hyperplasia involving sclerosing adenosis versus invasive lobular carcinoma; ; 9 Invasive carcinomas of no special type, special considerations; 9.1 Lymphovascular invasion versus retraction artifact; 9.2 Invasive micropapillary features versus retraction artifact; 9.3 No special type tumors with immunohistochemical evidence of neuroendocrine differentiation versus small cell carcinoma; 9.4 High grade carcinoma versus lymphoma; ; 10 Sentinel lymph nodes ; 10.1 Benign transport versus isolated tumor cell clusters; 10.2 Isolated tumor cells versus micrometastasis; 10.3 Micrometastasis versus capsular lymphatic involvement; 10.4 Micrometastasis versus benign glandular inclusion; ; 11 Vascular lesions of the breast; 11.1 Perilobular capillary hemangioma; 11.2 Atypical vascular lesion ; 11.3 Low grade angiosarcoma ; 11.4 High grade angiosarcoma; 11.5 Epithelioid angiosarcoma; ; """

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Author Information

Melinda E. Sanders, MD, is Associate Professor of Pathology, Microbiology and Immunology Anatomic Pathology Division, Subspecialty Consultant in Breast Pathology, Vanderbilt University Medical Center. Jean F. Simpson, MD, is President, Breast Pathology Consultants, Inc., Nashville, TN; and Adjunct Professor of Pathology, University of South Alabama, Mobile, Alabama David E. Elder, MB, ChB, is Professor of Pathology and Laboratory Medicine and Vice Chair for Anatomic Pathology at the Hospital of the University of Pennsylvania.

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