Anatomy of the nipple and breast ducts
Review Article

Anatomy of the nipple and breast ducts

Gustavo Zucca-Matthes1,2, Cícero Urban3, André Vallejo4

1Department of Gynaecology, Obstetrics and Mastology, School of Medicine of Botucatu, UNESP, Distrito de Rubine of Bot, Botucatu-SP, Brazil; 2Breast Unit, Barretos Cancer Hospital, Rua Antenor Villela Duarte, 1331, Barretos - SP, 14784-400, Brazil; 3Breast Unit, Nossa Senhora das Gras G Hospital, Curitiba, PR, Brazil; 4Breast Unit, Universidade Fluminense, Niterne, Rio de Janeiro, Brazil

Contributions: (I) Conception and design: G Zucca-Matthes; (II) Financial support: None; (III) Administrative support: None; (IV) Provision of study materials or patients: G Zucca-Matthes; (V) Collection and assembly of data: G Zucca-Matthes; (VI) Data analysis and interpretation: All authors; (VII) Manuscript writing: All authors; (VIII) Final approval of manuscript: All authors.

Correspondence to: Gustavo Zucca-Matthes, PhD, MD. Breast Unit, Barretos Cancer Hospital, Rua Antenor Duarte Villela, 1331, Barretos-SP, 17784-400, Brazil. Email: anguz75@gmail.com or zucca.mamarec@hcancerbarretos.com.br.

Abstract: Over time, variations of mastectomy came up and started allowing the oncological safety and the possibility of an immediate breast reconstruction. Nipple sparing mastectomy (NSM) procedures have strongly increased in frequency and have become one of the best alternatives to treat breast cancer, also improving overall aesthetic outcomes and the achievement of contralateral breast symmetry. The nipple areola-complex (NAC) must be considered the identity of the breast concerning self-esteem of patients. This paper will remind the main anatomical topics around the nipple and breast ducts.

Keywords: Breast; breast conserving treatment; mastectomy; mammoplasty; nipple; anatomy; breast cancer


Submitted Mar 13, 2015. Accepted for publication May 05, 2015.

doi: 10.3978/j.issn.2227-684X.2015.05.10


Introduction

Over time, variations of mastectomy came up and led to enhance the oncological safety and the possibility of an immediate breast reconstruction. Those techniques permit the conservation of skin, inframammary fold and specially the nipple areola complex (NAC) to achieve better outcomes.

Nowadays the number of publications describing a nipple sparing mastectomy (NSM) has strongly increased. Regarding self-esteem the nipple must be considered the identity of the breast. Therefore, in order to increasing safe indications of sparing NAC this paper will revise the main anatomical topics around the nipple and breast ducts.


History of the anatomy (1)

Several important remarks on the NAC anatomy were made by Sir Astley Cooper [1840]. Over the last 160 years some of the anatomy knowledge acquired has changed (2) since Cooper’s original work. For example, the glandular tissue is depicted as 15-20 lobes radiating out from the nipple, whereas Cooper stated that he observed up to 22 ducts leading to the nipple but considered that many of these ducts were not functional and that there were normally fewer than 12 patent ducts opening at the nipple.

Actually, the breast is described as being composed of glandular and adipose tissue held together by a loose framework of fibers called Cooper’s ligaments. Histological studies demonstrate that the lobes are composed of lobules, which consist of clusters of alveoli containing mammary secretory epithelial cells (3). The alveoli are connected to very small ducts that join to form larger ducts draining the lobules. These larger ducts finally merge to a unique duct for each lobe. Under the areola, this single duct is depicted as widening into a lactiferous sinus before narrowing at the base of the nipple and terminating at its orifice on the surface of the nipple (1,4). Adipose tissue of the breast is situated between lobes rather than within lobules.


Embryology (5)

The beginning of mastogenesis occurs around the sixth week of development. At 9 months there is a clear linear elevation, called “milk line”. By the eighth week, the mammary gland is formed from the thickening located in the epidermic “milk line” in the area of the final breast. There is a proliferation of basal cells that invade the underlying mesoderm and at the same time, it will occur a regression of mammary segment, yielding papillary primordium. After the 31st week of intrauterine life, papillary bag suffer occlusion, forming the NAC. The nipple will appear at time of birth.

The areola is recognized by forming a circular area free of hair sketches, also appearing branched glands around (Montgomery).


Nipple abnormality

These anomalies could be classified into multiple conditions.

  • Accessory nipple. One to five percent of the population, equal incidence in male and females. Usually found in the inframammary region, and are prone to the same diseases as normal nipples. Excision is only indicated for cosmetic purposes, discomfort during menstruation, anxiety, pain, or restriction of arm movement (6).
  • Athelia is characterized by the congenital absence of the nipple areolar complex with the presence of breast tissue (7). This condition can be inherited by autosomal dominant inheritance, or as a part of a syndrome (e.g., Poland’s).
  • Amastia is the complete absence of breast structures.
  • Amastia is the absence of breast tissue with preservation of the NAC.
  • Inverted nipple is a condition where the nipple, instead of pointing outward, is retracted into the breast. In some cases, the nipple will be temporarily protruded if stimulated, but in others, the inversion remains regardless of stimulus. Women and men can have inverted nipples. Most common nipple variations that women are born with are caused by short ducts or a wide areola muscle sphincter (8).

Anatomy of NAC (1,5)

The NAC comprises two basic structures: the areola and the nipple (Figure 1).

Figure 1 Schematic view of nipple areola-complex (NAC).

The areola has a round shape and a varying size, on average 3 to 6 centimeters, normally situated around the forth rib level. It has sebaceous glands that make projections on its surface, forming tubercle of morgani, or areolar glands, which during pregnancy become enlarged giving rise to tubercles of Montgomery.

Some authors believe that such structures represent accessory mammary glands and it has been observed milk secretion output with manual expression of these tubers (this supposition leads some surgeons to prefer the use of the skin sparing mastectomy instead of nipple or areola sparing mastectomies because of oncological concerns).

In the center of the areola emerges a papillar cylindrical formation varying in size, averaging 10 to 12 millimeters (mm) wide by 9 to 10 mm in height. Its skin is similar to the areola, but has no sebaceous glands. It has 10 to 20 corresponding pores as the output of the milk ducts.

The NAC has no subcutaneous tissue. The skin of the nipple rests on a thin layer of smooth muscle, areolar muscle fibers which are distributed in two directions: radial and circular. The muscle of Sappey responsible for circular fibers and the muscle of Meyerholz, formed by the radial fibers.

The areolar muscle is continued in the papilla with longitudinal and circular fibers surrounding the milk ducts along with connective tissue support. Its contraction is responsible for the ejection of secretion in the milk sinuses and for the telotism of the papilla, “mimicking an erection”.

Below the areolar muscle there is a thin layer of fat which disappears as it approaches the papilla. In this pre-mammary fat tissue layer vessels are found running on radiated sense.

Blood supply

The NAC is mainly supplied by internal mammary artery, also known as internal thoracic artery, which is branch of the subclavian artery. Internal mammary artery sends perforating branches along the first, second, third and fourth intercostal spaces, crossing the pectoralis major and irrigating the inner half of the breast, including the NAC. The intercostal arteries, which are branch of the aorta, also cross the pectoralis major and irrigate the deep surface of the breast, complementing the arterial vascularization of the NAC.

Venous drainage of breast is divided into two systems: superficial and deep. The superficial veins run along the anterior surface of the fascia, following the path of areola under the NAC, called venous plexus of Haller.

Recently the use of breast MRIs have become increasingly common in breast cancer work-up. Previously obtained breast MRIs may facilitate oncoplastic surgery by delineating the blood supply to the NAC. Seitz et al. (9) retrospectively reviewed 52 breasts underwent to breast MRI over 1-year period. Blood supply to the NAC was classified into five anatomic zones (“NACsomes”): medial (type I), lateral (type II), central (type III), inferior (type IV) and superior (type V). Twenty-eight breasts had type I only blood supply, 22 breasts had multi-zone blood supply (type I + II, n=20; type I + III, n=2), one breast had type II only blood supply, and a single breast had type III only blood supply. Anatomic symmetry was observed in 96% of patients. Superomedial source vessels supplying the NAC were predominant (Figure 2).

Figure 2 Schematic view of blood supply of NAC by “NACsomes” (Type I yellow—medial, Type II green—lateral, Type III pink—central, Type IV purple—inferior and Type V orange—superior).

Innervation

The skin surface of the breast is innervated by the first to sixth intercostal nerves and a supraclavicular branch of the superficial cervical plexus. The nipple is innervated by the fourth intercostal nerve. Objective investigations about the real impact of breast size on NAC sensibility threshold should be better clarified. Longo et al. (10) suggested that large and heavy breasts may potentially produce a chronic nerve traction injury, causing an inverse relationship between breast volume and sensibility. Concerning mammoplasty, the fibrotic scar at the areolar edges could be responsible for the progressive sensibility worsening over time 6 to 48 months. Another interesting mentioned phenomenon is neural organization in the somatosensory system after reduction mammoplasty. Phantom sensations are reported after partial and total breast amputation for cancer, possibly due to both rearranging of peripheral nerves and remapping on different subcortical and cortical somatosensory areas.

Lymphatic drainage

The lymphatic drainage of the breast is carried through superficial and deep plexus. Superficially, there are the areolar plexus and the subareolar plexus of Sappey. The subareolar plexus receives the glandular lymph vessels and they continue towards the papilla and the areolar plexus, finally reaching the lymph nodes into the axilla.


Nipple areola-complex (NAC) by ultrasound

Ramsay et al. used ultrasound imaging to re-investigate the anatomy of the lactating breast. They showed that the mean number of main ducts at base of nipple was 9.6 (range, 6-18) and 9.2 (range, 4-14) for the left breast and right breast, respectively, which was not significantly different. The common sac-like appearance of lactiferous sinuses under the areola was not observed during scanning. The mean number of ducts and the diameter of main ducts were not related to nipple diameter, areola radius or milk production for individual breasts (2).


Nipple and breast feeding

Characteristics of nipple are an important factor in the success of breast feeding. Minimum nipple length of seven millimeters has shown to be specific for a highly successful rate of breastfeeding (11). Short, flat, or inverted nipples can be related to physical and psychological negative effects for the breastfeeding mother.


Nipple-sparing mastectomy (NSM)

It is clear that when a total mastectomy is performed, the removal of the NAC increases the sensation of mutilation, and the risk of tumor involvement should be considered within the spectrum of lumpectomy, skin-sparing mastectomy, and modified-radical mastectomy. Controlled-trials have clearly demonstrated the oncologic equivalence of modified-radical and skin-sparing mastectomies, where the risk of future breast cancer occurrence is low but not zero (12,13).

Current reports on NSM are most common to single-institution series. However the number of NSM procedures has increased over the past years. Tumor involvement is reported in over 35% of the patients when tumor size is more than 2 cm, especially when the tumor is situated in the subareolar area (14). NSM can be performed for prophylactic mastectomy and the treatment of selected breast cancer with oncologic safety. The risk of skin and nipple necrosis is a frequent complication of NSM procedure, and it is usually related to the volume of breast removed (15).

Despite varying indications and surgical protocols reports of the development of cancer in the NAC following NSM are remarkably rare. Different aspects should be considered to be a selection criteria for NSM indication as well as primary tumors located outside the areola margins, no nipple retraction or bloody discharge from the nipple, no retro areolar microcalcifications, no inflammatory signs and no retro areolar tumor infiltration at the frozen section (13,16,17). In our experience the most important aspect to allow the indication for a NSM is the negative frozen subareolar biopsy area during the surgery. The rate of a positive subareolar biopsy ranges between 2.2% to 12% (13,18).

Tumoral aspects will be important to take into account when considering the indication of adjuvant therapies. Overall, NSM is associated with high patient satisfaction rates (19-22).


Tips

The NAC may host benign pathologies, especially during pregnancy and puerperium. In addition, it has an important role in breast surgery when tumors can be resected through an incision that circles the areola (periareolar or “round block technique”). This technique can be used in numerous types of breast surgery. It allows the scar to go up to the periareolar circle which is in itself generally inconspicuous. In cases of tumoral excision, the round block produces a discreet scar and a more regular breast contour (23). Scar in this region maintains good aesthetic. It is recommended that the incisions are made just outside the areola in darker-skinned patients and immediately inside the areola in lighter-skinned patients. This is because the lighter shade of scar tissue.


Conclusions

Development of the current practice depends on a solid knowledge. Consistent knowledge of the anatomy of the NAC allows surgeons to perform better surgical procedures decreasing the sensation of mutilation without decreasing the chance of cure. The NAC is undoubtedly the identity of the breast.


Acknowledgements

The authors appreciate the cooperation of all colleagues in the Breast Unit—Barretos Cancer Hospital.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Bannister LH, Berry MM, Collins P, et al, editors. Gray’s Anatomy. 38th ed. New York: Churchill Livingstone, 1995:417-24.
  2. Ramsay DT, Kent JC, Hartmann RA, et al. Anatomy of the lactating human breast redefined with ultrasound imaging. J Anat 2005;206:525-34. [PubMed]
  3. Tobon H, Salazar H. Ultrastructure of the human mammary gland. II. Postpartum lactogenesis. J Clin Endocrinol Metab 1975;40:834-44. [PubMed]
  4. Vorherr H. The Breast: morphology, physiology and lactation. London, UK: Academic Press, 1974.
  5. Franco JM. Mastologia: formação do especialista. 1st ed. São Paulo: Atheneu, 1997.
  6. Aydogan F, Baghaki S, Celik V, et al. Surgical treatment of axillary accessory breasts. Am Surg 2010;76:270-2. [PubMed]
  7. Trier WC. Complete breast absence. Case report and review of the literature. Plast Reconstr Surg 1965;36:431-9. [PubMed]
  8. Alexander JM, Grant AM, Campbell MJ. Randomised controlled trial of breast shells and Hoffman’s exercises for inverted and non-protractile nipples. BMJ 1992;304:1030-2. [PubMed]
  9. Seitz IA, Nixon AT, Friedewald SM, et al. “NACsomes”: A new classification system of the blood supply to the nipple areola complex (NAC) based on diagnostic breast MRI exams. J Plast Reconstr Aesthet Surg 2015;68:792-9. [PubMed]
  10. Longo B, Campanale A, Farcomeni A, et al. Long-term sensory recovery of nipple-areola complex following superolateral pedicled reduction mammaplasty. Plast Reconstr Surg 2013;132:735e-742e. [PubMed]
  11. Puapornpong P, Raungrongmorakot K, Paritakul P, et al. Nipple length and its relation to success in breastfeeding. J Med Assoc Thai 2013;96 Suppl 1:S1-4. [PubMed]
  12. Petit JY, Veronesi U, Orecchia R, et al. Nipple-sparing mastectomy in association with intra operative radiotherapy (ELIOT): A new type of mastectomy for breast cancer treatment. Breast Cancer Res Treat 2006;96:47-51. [PubMed]
  13. Spear SL, Willey SC, Feldman ED, et al. Nipple-sparing mastectomy for prophylactic and therapeutic indications. Plast Reconstr Surg 2011;128:1005-14. [PubMed]
  14. Agarwal S, Agarwal S, Neumayer L, et al. Therapeutic nipple-sparing mastectomy: trends based on a national cancer database. Am J Surg 2014;208:93-8. [PubMed]
  15. Chirappapha P, Petit JY, Rietjens M, et al. Nipple sparing mastectomy: does breast morphological factor related to necrotic complications? Plast Reconstr Surg Glob Open 2014;2:e99. [PubMed]
  16. Vlajcic Z, Zic R, Stanec S, et al. Nipple-areola complex preservation: predictive factors of neoplastic nipple-areola complex invasion. Ann Plast Surg 2005;55:240-4. [PubMed]
  17. Lohsiriwat V, Petit J. Nipple Sparing Mastectomy: from prophylactic to therapeutic standard. Gland Surg 2012;1:75-9. [PubMed]
  18. Kneubil MC, Lohsiriwat V, Curigliano G, et al. Risk of locoregional recurrence in patients with false-negative frozen section or close margins of retroareolar specimen in nipple-sparing mastectomy. Ann Surg Oncol 2012;19:4117-23. [PubMed]
  19. Yueh JH, Houlihan MJ, Slavin SA, et al. Nipple-sparing mastectomy: evaluation of patient satisfaction, aesthetic results, and sensation. Ann Plast Surg 2009;62:586-90. [PubMed]
  20. Didier F, Arnaboldi P, Gandini S, et al. Why do women accept to undergo a nipple sparing mastectomy or to reconstruct the nipple areola complex when nipple sparing mastectomy is not possible? Breast Cancer Res Treat 2012;132:1177-84. [PubMed]
  21. Didier F, Radice D, Gandini S, et al. Does nipple preservation in mastectomy improve satisfaction with cosmetic results, psychological adjustment, body image and sexuality? Breast Cancer Res Treat 2009;118:623-33. [PubMed]
  22. Zucca-Matthes G, Manconi A, da Costa Viera RA, et al. The evolution of mastectomies in the oncoplastic breast surgery era. Gland Surg 2013;2:102-6. [PubMed]
  23. Benelli L. A new periareolar mammaplasty: the “round block” technique. Aesthetic Plast Surg 1990;14:93-100. [PubMed]
Cite this article as: Zucca-Matthes G, Urban C, Vallejo A. Anatomy of the nipple and breast ducts. Gland Surg 2016;5(1):32-36. doi: 10.3978/j.issn.2227-684X.2015.05.10