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Breast Cancer: The Path to Diagnosis

Medically reviewed by Maybell Nieves, M.D.
Written by Kelly Crumrin
Updated on August 22, 2024

Catching breast cancer early improves the chances of treating it effectively. Breast cancer is often identified during a routine screening mammogram. Some people might go to their doctor after they notice symptoms of breast cancer during a regular monthly self-exam.

If a doctor suspects you might have breast cancer, they will usually refer you to a cancer specialist known as an oncologist. Specialists who treat breast cancer include medical oncologists, surgical oncologists, radiation oncologists, geneticists, pathologists, psycho-oncologists, and plastic surgeons. Multiple specialists often work together as a team to treat people with breast cancer. A medical oncologist is usually the doctor who diagnoses breast cancer and manages the treatment process.

How Is Breast Cancer Diagnosed?

Breast cancer is usually suspected after a mass in the breast tissue is identified. Since treatment is more effective the earlier the breast cancer is diagnosed, most doctors will want to schedule tests as soon as possible.

Tests and What They Show

Imaging scans can show the shape, size, and location of potential tumors, but only a biopsy and pathology report can provide conclusive results on whether tissue is breast cancer or not. Laboratory exams, genetic tests, blood tests, and other tests help the oncologist better understand the type of breast cancer as well as its stage and grade.

Imaging Tests

If a tumor is felt during self-exam or identified by a screening mammogram, it is not necessarily breast cancer. Imaging tests are often the first step in checking a suspicious lump. The results of an imaging test may make a diagnosis of breast cancer more or less likely.

The most common imaging test used for suspected breast cancer is a diagnostic mammogram. Both screening and diagnostic mammograms use X-rays to image the tissue of the breast. In a diagnostic mammogram, the technician takes many more images of the breast — including more angles and views. Other imaging tests used to diagnose breast cancer can include ultrasound and magnetic resonance imaging (MRI). Imaging tests are often painless or may cause minimal discomfort.

Biopsy

If breast cancer was not ruled out by the results of imaging exams, the doctor will likely perform a biopsy. Less than 25 percent of breast biopsies show growths that are cancerous (also known as invasive or malignant).

Taking a biopsy — a sample of suspected cells — is the only certain way to diagnose breast cancer. There are several techniques used to biopsy breast tissue. Lymph nodes in the chest or under the arm may also be biopsied to check for any trace of cancer cells.

Needle biopsy is one of the most common and least invasive methods for breast biopsy. First, your breast will be numbed. A hollow needle will be inserted one or more times into the breast to remove tiny amounts of breast tissue. Needle biopsy may be uncomfortable, but it leaves no scar.

If needle biopsy is inconclusive, the doctor may perform an incisional or excisional biopsy. In these types of biopsy, you will receive medication to sedate you. The doctor will use a scalpel to cut into the breast. Incisional biopsy removes a smaller piece of tissue. Excisional biopsy is more involved; the doctor will remove a larger piece of cancerous tissue along with a rim of normal tissue around it. Incisional and excisional biopsies usually leave a scar.

Blood Tests

The doctor may order blood tests to check the function of your bone marrow, liver, and kidneys. Blood tests may also check for hepatitis. If the test results show any problems, it may influence the doctor’s treatment recommendations.

Laboratory Testing

Biopsied tissue will be examined in the pathology lab. The pathologist will view the tissue samples under the microscope to determine whether it is cancerous, and if so, what grade the tumor should be assigned.

If the tissue is cancerous, the cells will be analyzed to determine whether they are positive or negative for estrogen, progesterone, or human epidermal growth factor receptor 2 (HER2) receptors. The results of this analysis decide the molecular subtype of the cancer.

Genomic tests such as Oncotype DX will evaluate genes in the cancer cells and provide detailed predictions about how the tumor is likely to grow, how effective some treatments will be, and the odds of the tumor returning later on.

Results of the biopsy and Oncotype DX reports provide vital information the oncologist needs to stage the tumor and make recommendations on which treatments will be most effective.

Talk With Others Who Understand

MyBCTeam is the social network for people with breast cancer and their loved ones. On MyBCTeam, more than 72,000 members come together to ask questions, give advice, and share their stories with others who understand life with breast cancer.

Have you been diagnosed with breast cancer? What tests were helpful for you? Do you have any advice for others undergoing testing? Share your experiences in the comments below, or start a conversation by posting on MyBCTeam.

Updated on August 22, 2024

A MyBCTeam Member

Go girl ,they say it really helps

May 11, 2022
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Is A CA 29-27 Result Of 44.5 High? I Know It Should Be 0-38, But Does This Fluctuate?

June 29, 2024 by A MyBCTeam Member 4 answers
Maybell Nieves, M.D. graduated from Central University of Venezuela, where she completed medical school and general surgery training. Learn more about her here.
Kelly Crumrin is a senior editor at MyHealthTeam and leads the creation of content that educates and empowers people with chronic illnesses. Learn more about her here.

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