Escaping from Flatland: clinical and biological aspects of human mammary duct anatomy in three dimensions

Accurate knowledge of breast duct anatomy in three dimensions is needed to understand normal breast development, how intraepithelial neoplasia may spread through a breast, and the potential for diagnostic and therapeutic access to breast parenchyma via the nipple. This paper reports three related exploratory studies. In study 1, the median number of milk‐collecting ducts in the nipple was determined in 72 breasts excised for cancer; in study 2, the volumes of all 20 complete duct systems (‘lobes’) in an autopsy breast were measured from 2 mm serial ‘subgross’ sections; and in study 3, a 3D digital model of all collecting ducts in a mastectomy nipple was made from 68 100 µm serial sections. The mastectomy nipples contained 11–48 central ducts (median 27, inter‐quartile range 21–30). In the autopsy breast, the largest ‘lobe’ drained 23% of breast volume; half of the breast was drained by three ducts and 75% by the largest six. Conversely, eight small duct systems together accounted for only 1.6% of breast volume. The 3D model of the nipple revealed three distinct nipple duct populations. Seven ducts maintained a wide lumen up to the skin surface (population A); 20 ducts tapered to a minute lumen at their origin in the vicinity of skin appendages (population B) on the apex of the nipple; and a minor duct population (C) arose around the base of the papilla. Major variations in duct morphology and extent define highly variable territories in which intraepithelial neoplasia could grow. While population A ducts appear accessible to duct endoscopy or lavage, population B and population C ducts may be less accessible. Copyright © 2004 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

[1]  A. Dixson,et al.  Masculine Somatotype and Hirsuteness as Determinants of Sexual Attractiveness to Women , 2003, Archives of sexual behavior.

[2]  Seiichi Takenoshita,et al.  Computer‐assisted complete three‐dimensional reconstruction of the mammary ductal/lobular systems , 2001, Cancer.

[3]  Christopher B Umbricht,et al.  Detection of breast cancer cells in ductal lavage fluid by methylation-specific PCR , 2001, The Lancet.

[4]  A. Roulin,et al.  Female barn owls (Tyto alba) advertise good genes , 2000, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[5]  Johannes Streicher,et al.  A new episcopic method for rapid 3-D reconstruction: applications in anatomy and embryology , 1998, Anatomy and Embryology.

[6]  Sanford H Barsky,et al.  Breast-duct endoscopy to study stages of cancerous breast disease , 1996, The Lancet.

[7]  J. Going,et al.  Three dimensional anatomy of complete duct systems in human breast: pathological and developmental implications. , 1996, Journal of clinical pathology.

[8]  M. Halliwell,et al.  Atlas of Ultrasound and Ductal Echography of the Breast: the Introduction of Anatomic Intelligence Into Breast Imaging , 1995 .

[9]  A. Møller,et al.  Female swallow preference for symmetrical male sexual ornaments , 1992, Nature.

[10]  W. M. Morek,et al.  Breast Volume Measurement of 598 Women Using Biostereometric Analysis , 1989, Annals of plastic surgery.

[11]  H J Gundersen,et al.  The efficiency of systematic sampling in stereology and its prediction * , 1987, Journal of microscopy.

[12]  E. Robecchi [Pathology of the breast]. , 1954, Minerva ginecologica.

[13]  E. Piette,et al.  A Textbook of Histology , 1936, The Indian Medical Gazette.

[14]  Tumours of the Breast: Their Pathology, Symptoms, Diagnosis and Treatment , 1932, The Indian Medical Gazette.

[15]  W. Weninger,et al.  Phenotyping transgenic embryos: a rapid 3-D screening method based on episcopic fluorescence image capturing , 2002, Nature Genetics.

[16]  D. Cosgrove The breast , 1999, European Radiology.

[17]  A. Møller Stress, developmental stability and sexual selection. , 1997, EXS.