Paget's Disease of the Breast
Paget's Disease of the Breast
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Paget's Disease of the Breast is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- mammary Paget's disease
- Paget's disease of the nipple
- Paget's disease of the nipple and areola
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
Paget's disease of the breast is a rare form of breast cancer that almost exclusively occurs in women. However, rare cases have been reported in men. Paget's disease of the breast is characterized by inflammatory, "eczema-like" changes of the nipple that may extend to involve the areola, which is the circular, darkened (pigmented) region of skin surrounding the nipple. Initial findings often include itching (pruritus), scaling, and crusting of and/or discharge from the nipple. In individuals with Paget's disease of the breast, distinctive tumor cells (known as Paget cells) are present within the outermost layer of skin (epidermis) of the nipple, when viewed under a microscope. Most women with this disorder have an underlying cancer (malignancy) affecting the milk ducts (ductal carcinoma). The milk ducts are the channels that carry milk secreted by lobes of the breast to the nipple. The exact cause of Paget's disease of the breast is not fully understood.
Paget's disease of the breast was originally reported in 1874 by Sir James Paget, an English surgeon, who also described an unrelated skeletal condition known as Paget's disease of the bone. It is essential to note that these disorders are distinct entities that are medically unrelated.
Paget's disease of the breast is a malignant (cancerous) condition that initially appears as chronic, inflammatory, "eczema-like" changes of the nipple and adjacent areas.
In individuals with Paget's disease of the breast, initial characteristic skin changes may include the appearance of reddish (erythematous), scaling, crusting, and/or abnormally thickened skin patches (plaques) or lesions on the nipple that may extend to adjacent areas of the areola. Some affected individuals may also have abnormal discharge from the nipple. Additional symptoms may include itching (pruritus) or burning sensations and/or oozing or bleeding of the affected area. Eventually, pain and sensitivity of the affected area may be present. Early on, the skin symptoms of Paget's disease of the breast may fluctuate, improving only to worsen again. Paget's disease of the breast usually affects one breast (unilateral), but there are rare cases in which both breasts are involved (bilateral).
The initial skin changes of Paget's disease of the breast may appear relatively benign and many individuals may overlook such symptoms, mistakenly attributing them to an inflammatory skin condition or infection. As a result, diagnosis may be delayed, often up to six months or more. Most individuals with the condition eventually seek medical attention due to associated itching or burning sensations, soreness, or pain of the affected area.
Most women with Paget's disease of the breast have an underlying malignancy, which may be completely contained within the milk ducts (ductal carcinoma in situ) or may have invaded the surrounding tissue, potentially spreading to the lymph nodes under the arms (axillary lymph nodes) and other regions of the body (metastatic disease).
Approximately 50 percent or more of affected individuals may have a lump or mass that may be felt (palpated) below the nipple. Some individuals with Paget's disease of the breast may have additional symptoms or physical findings. For example, in some instances, the nipple may turn inward (retracted nipple).
The overall disease course may vary greatly from one person to another, depending upon the nature and size of an underlying malignancy, whether a palpable breast tumor is present upon diagnosis, whether metastatic disease is present, specific treatment measures followed, and other possible factors.
Two main theories have been proposed to explain the development of Paget's disease of the breast. One theory suggests that distinctive cancer cells called Paget's cells break off from an underlying tumor or malignancy within the breast and travel through the milk ducts to the nipples. Supportive evidence includes laboratory studies demonstrating that Paget cells and the underlying breast cancer share certain characteristics, thus appearing to originate from the same cell population. In addition, malignant cells have been shown to extend along breast ductal tissue from the underlying breast tumor to the nipple. Accordingly, many researchers have concluded that Paget cells appear to be derived from the lining (epithelium) of the milk ducts, invading and multiplying (proliferating) within the surface tissue (epidermis) of the nipple and adjacent areas of the areola. This theory explains why most individuals with Paget's disease of the breast have an underlying form of cancer.
The second theory suggests that the presence and spread of Paget cells represents a distinct disease process originating in the outer skin layer of the nipple. The malignant changes occur without warning and for no known reason (spontaneously). This theory would explain the rare cases where no underlying malignancy is present or where the underlying malignancy is a different tumor type.
As with other cancers, the exact underlying cause or causes of malignancy associated with Paget's disease of the breast remain unknown. Researchers speculate that genetic and immunologic abnormalities, environmental factors (e.g., exposure to ultraviolet rays, certain chemicals and ionizing radiation), diet, stress, and/or other factors may play contributing roles in causing specific types of cancer. Investigators at the National Cancer Institute and elsewhere are conducting ongoing basic research to learn more about the many factors that may result in cancer.
In individuals with cancer, including breast malignancies, tumor development results from abnormal changes in the structure of certain cells. The specific cause of such changes is unknown. However, current research suggests that abnormalities of DNA (deoxyribonucleic acid), which is the carrier of the body's genetic code, are the underlying basis of cellular malignant transformation. In many cases, these abnormal changes may appear to occur spontaneously for unknown reasons (sporadically).
Cells that undergo malignant transformation typically revert to a less specialized, more primitive form (anaplasia or loss of differentiation), meaning that they are no longer capable of performing their intended, specialized functions within the tissue in question. Malignant cells pass their abnormal changes on to their "daughter" cells and typically grow and divide at an unusually rapid, uncontrolled rate. This uncontrolled cellular growth may eventually result in invasion of surrounding tissues, infiltration of regional lymph nodes, and spread of the malignancy (metastasis) via the bloodstream, the lymphatic circulation, or other means.
Paget's disease of the breast is a rare form of breast cancer that almost exclusively affects women. However, there have been rare cases in which the disorder has occurred in men. Paget's disease of the breast most commonly affects middle-aged individuals, primarily occurring between 50 to 60 years of age, although it has been reported in individuals in their 20s. It is thought to represent less than 5 percent of all breast cancers. The exact prevalence and incidence of Paget's disease of the breast in the general population is unknown.
Symptoms of the following disorders may be similar to those of Paget's disease of the breast. Comparisons may be useful for a differential diagnosis:
Extramammary Paget's disease (EMPD) is characterized by the development of a reddish, scaling lesion that resembles that seen in Paget's disease of the breast but does not occur on the breasts. The term extramammary refers to regions other than or outside of the breasts. In those with EMPD, additional symptoms and findings may include itching, burning, pain, and/or bleeding of the affected area. EMPD often involves the female or male external genitals (e.g., vulva, glans penis) and/or the region around the anus (perianal region). EMPD of the vulva is associated with an underlying cancer (carcinoma) in about 30 percent of cases; involvement of the perianal area is associated with a distant or underlying carcinoma in up to approximately 73 percent of cases.
Eczema is a common inflammatory condition characterized by itching (pruritus) and redness (erythema) of upper skin layers (i.e., superficial dermatitis). The condition is also often associated with blistering or scabbing, scaling, oozing, crusting, and thickening of affected skin areas. There are multiple types of eczema that may result from various internal (endogenous) and/or external (exogenous) factors, including an excessive immune response to certain, usually environmental agents.
Bowen disease is a rare skin disorder. Affected individuals develop a slow-growing, reddish scaly patch or plaque on the skin. Sun exposed areas of the skin are most often affected. Bowen disease only affects the outermost layer of the skin (epidermis). Lesions are usually not painful or may not be associated with any symptoms (asymptomatic). In most cases, treatment is highly successful. Bowen disease is considered a pre-cancerous condition, although the risk of developing skin cancer is less than 10 percent. The disorder usually affects older adults. The exact cause of Bowen disease is unknown, although there are identified risk factors such as chronic sun exposure. (For more information on this disorder, choose "Bowen" as your search term in the Rare Disease Database.)
Malignant melanoma is a form of skin cancer that develops from the melanin cells of the upper layer of the skin (epidermis) or from similar cells that may be found in moles (nevi). In early stages most melanomas do not produce any specific symptoms. Later, they may appear as lesions that do not heal or as existing moles that show changes in size or color. This type of skin cancer eventually spreads to the lower skin levels and adjacent tissue and may result in new tumor growths in vital organs of the body. (For more information on this disorder, choose "malignant melanoma" as your search term in the Rare Disease Database.)
Paget's disease of the breast is diagnosed based upon thorough clinical examination, identification of characteristic physical findings, a complete patient history, and a variety of specialized tests. The disorder can be confused with other skin conditions such as eczema potentially causing a delay in the diagnosis.
Clinical Testing and Work-Up
Tests that may be used to help diagnose Paget's disease of the breast include blood tests, surgical removal (biopsy) and microscopic examination of affected breast tissue, mammography or specialized x-ray imaging of the breasts, and/or microscopic evaluation of any nipple discharge for cancerous cells (cytologic smear).
During a biopsy a small sample of breast tissue is taken and examined under a microscope to determine whether Paget cells are present. If a lump is found in the breast, a sample of that tissue will also be taken.
A mammography is an x-ray of the breast tissue and may be used to determine whether Paget cells are present. A mammography is also used to detect or rule out whether an underlying cancer is present. Additional specialized imaging techniques such as an ultrasound or magnetic resonance imaging (MRI) may be used to create additional images of the breast and to determine whether an underlying cancer is present.
If nipple discharge is present, a sample may be taken and studied to detect the presence of Paget cells.
If affected individuals have an underlying invasive cancer, then a sentinel lymph node biopsy may be performed. During this biopsy, a sample of tissue is taken from the lymph nodes under the armpits (axillary lymph nodes) to check and see whether cancer has spread to this area. A physician will locate and remove the sentinel lymph node, which refers to the first (or first few) lymph node(s) to which cancer cells are most likely to spread.
The therapeutic management of individuals with Paget's disease of the breast may require the coordinated efforts of a team of medical professionals, such as physicians who specialize in the diagnosis and treatment of cancer (medical oncologists), specialists in the use of radiation to treat cancer (radiation oncologists), surgeons, oncology nurses and other healthcare professionals.
Specific therapeutic procedures and interventions may vary, depending upon numerous factors, such as extent of the primary tumor (stage) and degree of malignancy (grade); the nature, size, and invasiveness of an underlying breast malignancy and the presence or absence of metastatic disease; individual's age and general health; and/or other elements. Decisions concerning the use of particular interventions should be made by physicians and other members of the health care team in careful consultation with the patient, based upon the specifics of his or her case; a thorough discussion of the potential benefits and risks; patient preference, and other appropriate factors.
Treatment has traditionally included surgical removal of breast tissue, adjacent lymph nodes, and, in some cases, underlying muscles of the upper chest wall and other tissues (modified radical or radical mastectomy). Some individuals may only require a simple mastectomy, in which the breast and the lining over the chest muscles are removed.
In selected cases where there is no palpable breast mass and negative mammograms, or in those with disease confined to the nipple and areola, conservative tissue-sparing surgery (lumpectomy) may be recommended. During this surgery, the nipple and areola are removed along with a small section of breast tissue. A physician will attempt to remove as little breast tissue as necessary. Individuals who received a lumpectomy will receive follow up radiation therapy.
Individuals with Paget's disease of the breast will receive additional, supportive therapy called adjuvant therapy that is designed to complement surgery and prevent the cancer from recurring. Adjuvant therapy may include radiation therapy, anti-cancer drugs (chemotherapy) and hormone therapy.
Photodynamic therapy (PDT), a procedure in which a drug known as a photosensitizer is used along with a special type light, has been used to treat some individuals with Paget's disease of the breast. During photodynamic therapy, the drug is administered to an affected individual and absorbed by the affected cells. A specific wavelength of light is used to active the drug which binds with oxygen creating a chemical that destroys the affected cells. Initial results have shown that PDT is safe, well tolerated and may be a less invasive alternative therapy for individuals with Paget's disease of the breast. However, studies so far have been limited and more research is necessary to determine the long-term safety and effectiveness off PDT for the treatment of individuals with Paget's disease of the breast.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Toll-free: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Fouad D. Paget's disease of the breast in a male with lymphomatoid papulosis: a case report. J Med Case Reports. 2011;5:43. http://www.ncbi.nlm.nih.gov/pubmed/21276228
Nardelli AA, Stafinski T, Menon D. Effectiveness of photodynamic therapy for mammary and extra-mammary Paget's disease: a state of the science review. BMC Dermatol. 2011;11:13. http://www.ncbi.nlm.nih.gov/pubmed/21676258
Siponen E, Hukkinen K, Heikkila P, Joensuu H, Leidenius M. Surgical treatment in Paget's disease of the breast. Am J Surg. 2011;200:241-246. http://www.ncbi.nlm.nih.gov/pubmed/20678619
Seetharam S, Fentiman IS. Paget's disease of the nipple. Women's Health. 2009;5:397-402.
Caliskan M, Gatti G, Sosnovskikh I, et al. Paget's disease of the breast: the experience of the European Institute of Oncology and review of the literature. Breast Cancer Res Treat. 2008;112:513-521. http://www.ncbi.nlm.nih.gov/pubmed/18240020
Subramanian A, Birch H, McAvinchey R, Stacey-Clear A. Paget's disease of uncertain origin. Int Semin Surg Oncol. 2007;4:12. http://www.ncbi.nlm.nih.gov/pubmed/17480238
Laronga C, Hasson D, Hoover S, et al. Paget's disease in the era of sentinel lymph node biopsy. Am J Surg. 2006;192:481-483. http://www.ncbi.nlm.nih.gov/pubmed/16978954
Marcus E. The management of Paget's disease of the breast. Curr Treat Options Oncol. 2004;5:153-160. http://www.ncbi.nlm.nih.gov/pubmed/14990209
Sakorafas GH, Blanchard K, Sarr MG, Farley DR. Paget's disease of the breast. Cancer Treat Rev. 2001;27:9-18. http://www.ncbi.nlm.nih.gov/pubmed/11735019
Bodnar M, Miller OF 3rd, Tyler W. Paget's disease of the male breast associated with intraductal carcinoma. J Am Acad Dermatol. 1999;40:829-831. http://www.ncbi.nlm.nih.gov/pubmed/10321627
Kollmorgen DR, Varanasi JS, Edge BS, Carson WE 3rd. Paget's disease of the breast: a 33-year experience. J Am Coll Surg. 1998;187:171-177. http://www.ncbi.nlm.nih.gov/pubmed/9704964
Mayo Clinic for Medical Education and Research. Paget's Disease of the Breast. August 24, 2010. Available at: http://www.mayoclinic.com/health/pagets-disease-of-the-breast/DS00771 Accessed On: September 6, 2011.
National Cancer Institute. Paget's Disease of the Nipple. June 27, 2005. Available at: http://www.cancer.gov/cancertopics/factsheet/Sites-Types/paget-breast Accessed On: August 31, 2011.
Kao GF. Mammary Paget Disease. Emedicine Journal, Dec 17, 2009. Available at: http://emedicine.medscape.com/article/1101235-overview Accessed on: August 31, 2011.
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