Breast cancer: Pathology review

Last updated: January 15, 2024

Breast cancer: Pathology review

Exam 1 -AHN 548 -

Exam 1 -AHN 548 -

Anatomy of the breast
Anatomy clinical correlates: Breast
Mammary gland histology
Ovary histology
Fallopian tube and uterus histology
Cervix and vagina histology
Anatomy and physiology of the female reproductive system
Puberty and Tanner staging
Estrogen and progesterone
Menstrual cycle
Menopause
Pregnancy
Oxytocin and prolactin
Breastfeeding
Stages of labor
Precocious puberty
Delayed puberty
Klinefelter syndrome
Turner syndrome
5-alpha-reductase deficiency
Androgen insensitivity syndrome
Kallmann syndrome
Amenorrhea
Ovarian cyst
Premature ovarian failure
Ovarian torsion
Polycystic ovary syndrome
Krukenberg tumor
Ovarian sex-cord stromal tumors
Ovarian surface epithelial tumors
Ovarian germ cell tumors
Uterine fibroid
Endometriosis
Endometritis
Endometrial hyperplasia
Choriocarcinoma
Endometrial cancer
Cervical cancer
Pelvic inflammatory disease
Urethritis
Mastitis
Fibrocystic breast changes
Phyllodes tumor
Intraductal papilloma
Paget disease of the breast
Breast cancer
Gestational hypertension
Hyperemesis gravidarum
Preeclampsia & eclampsia
Gestational diabetes
Placenta previa
Placenta previa
Cervical incompetence
Placenta accreta
Placental abruption
Oligohydramnios
Polyhydramnios
Potter sequence
Intrauterine growth restriction
Preterm labor
Postpartum hemorrhage
Chorioamnionitis
Congenital toxoplasmosis
Congenital syphilis
Congenital cytomegalovirus (NORD)
Neonatal conjunctivitis
Neonatal herpes simplex
Neonatal sepsis
Congenital rubella syndrome
Neonatal meningitis
Miscarriage
Gestational trophoblastic disease
Ectopic pregnancy
Fetal alcohol syndrome
Uterine disorders: Pathology review
Cervical cancer: Pathology review
Benign breast conditions: Pathology review
Ovarian cysts and tumors: Pathology review
Vaginal and vulvar disorders: Pathology review
Breast cancer: Pathology review
Complications during pregnancy: Pathology review
Congenital TORCH infections: Pathology review
Amenorrhea: Pathology review
Estrogens and antiestrogens
Androgens and antiandrogens
Uterine stimulants and relaxants
Progestins and antiprogestins
Aromatase inhibitors
Prolactinoma
Breast cancer: Clinical
Abnormal uterine bleeding: Clinical
Cervical cancer: Clinical
Genito-pelvic pain and penetration disorder
Sexual dysfunctions: Clinical
Infertility: Clinical
Amenorrhea: Clinical
Contraception: Clinical
Physical and sexual abuse
Sexual orientation and gender identity
Female sexual interest and arousal disorder
Orgasmic dysfunction
Ovarian cysts, cancer, and other adnexal masses: Clinical
Vulvovaginitis: Clinical
Hypertensive disorders of pregnancy: Clinical
Perinatal infections: Clinical
Gestational trophoblastic disease: Clinical
Routine prenatal care: Clinical
Abnormal labor: Clinical
Neonatal jaundice: Clinical
Streptococcus agalactiae (Group B Strep)
Neonatal hepatitis
Neonatal respiratory distress syndrome
Jaundice
Jaundice: Clinical
Enuresis
Nocturnal enuresis
Elimination disorders: Clinical
Biliary colic
Night terrors
ADHD: Information for patients and families (The Primary School)
Attention deficit hyperactivity disorder
Autism spectrum disorder
Fragile X syndrome
Precocious and delayed puberty: Clinical
Constitutional growth delay
Inheritance patterns
Mendelian genetics and punnett squares
Mitochondrial myopathy
Body dysmorphic disorder
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Cri du chat syndrome
DiGeorge syndrome
Williams syndrome
Neurofibromatosis
Marfan syndrome
Achondroplasia
Osteogenesis imperfecta
Craniosynostosis
Myelodysplastic syndromes
Cystic fibrosis
Cystic fibrosis: Pathology review
Cystic fibrosis: Clinical
Alport syndrome
Spinal muscular atrophy
Muscular dystrophy
Hemophilia
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
Acute intermittent porphyria
Familial hypercholesterolemia
Gaucher disease (NORD)
Cleft lip and palate
Spina bifida
Developmental milestones: Clinical

Questions

USMLE® Step 1 style questions USMLE

0 of 14 complete

Start
A 62-year-old woman comes to the clinic due to a breast lump she felt while showering. Medical history is significant for hyperlipidemia and hypertension, which is managed with lovastatin and hydrochlorothiazide, respectively. Vitals are within normal limits. On physical examination, a lump in the right upper quadrant of the right breast and a palpable axillary lymph node are noted. She is sent for a mammography, which reveals no abnormalities. Ultrasound is obtained and shows a mass lesion. Core needle biopsy reveals cells that invaded the stroma aligned in a “single-file,” as depicted by the following image:

Reproduced from: Wikimedia Commons

Which of the following is the most likely diagnosis?  

Transcript

Watch video only

64-year-old Cassie comes to the office because of a new breast mass that she found on her monthly self-examination.

A mammogram shows microcalcification clusters so an excisional biopsy is performed.

Pathology shows high-grade cells with central necrosis in the lumen and dystrophic calcification in the center of the ducts without invasion of the basement membrane.

Later that day, a 58-year-old named Linda comes to the physician's office with eczematous dermatitis of the left nipple and areolar area for the past 24 months.

Her history reveals that the lesion has been treated unsuccessfully with topical steroids and has progressively distorted the nipple, resulting in nipple inversion.

Physical examination reveals scaly, crusted, and deformed left nipple with multiple plaques overlying the surrounding areola.

At first glance, you’d think Cassie and Linda have nothing in common, but the fact is, they have different forms of breast cancer!

Breast cancer is the most common malignancy in women and it’s typically seen in postmenopausal women, over 50 years of age.

Most breast cancers are adenocarcinomas and they typically arise from the terminal duct lobular units.

Breast cancer can present as a palpable hard mass, most commonly located in the upper outer quadrant of the breast.

Now, some breast cancers can be associated with amplification and overexpression of genes for estrogen receptors, progesterone receptors, and HER2/neu receptors.

For your exam, you have to remember that these receptors are important therapeutic and prognostic factors of breast cancer.

In other words, breast cancers that are associated with overexpression of estrogen and progesterone receptors are more susceptible to anti-estrogen medications, such as tamoxifen.

On the other hand, HER2/neu receptors, also known as erbB2 receptors, are coded by the ERB-B2 gene.

These receptors are transmembrane glycoproteins with tyrosine kinase activity that plays an important role in epithelial growth and differentiation.

HER2/neu receptors are present in small amounts in normal breast and ovarian cells; while they are overexpressed in 25-30% of breast cancers as well as in adenocarcinomas of the ovary, lung, stomach, and salivary glands.

Moreover, breast cancers that are associated with HER2/neu positivity are linked to more aggressive tumors; however, they are more likely to respond to anti-HER-2 monoclonal antibodies, like trastuzumab.

Another high-yield fact is that breast cancers that are estrogen negative, progesterone negative, and HER2/neu negative, or in other words, triple-negative, are linked to a more aggressive form of breast cancer.

Finally, breast cancer tends to metastasize first to the axillary lymph nodes, while in the later stages, the most common sites of metastases include lungs, liver, and bones.

Now, switching gears and moving on to risk factors!

The most common risk factors in females include advanced age and family history of breast cancer, which is considered the strongest risk factor.

The risk of hereditary breast cancer is increased even more in young women who have had more than one close relative with premenopausal breast cancer.

Also, a family history of ovarian cancer is linked to an increased risk for ovarian and breast cancer, because both of these cancers are associated with autosomal dominant mutations of BRCA1 and BRCA2 genes. BRCA genes codes for BRCA proteins that acts as a tumor suppressor that controls the cell cycle, helps repair DNA, and regulates transcription of DNA.

Moreover, women with the BRCA1 mutation have a 70-80% higher risk for developing breast cancer; and a 40% increased risk for developing ovarian cancer compared to women without the BRCA1 mutation.

Another commonly high yield factor on your exam is increased estrogen exposure like nulliparity, late first pregnancy, early menarche, and late menopause.

Other risk factors include alcohol consumption, absence of breastfeeding, and obesity in postmenopausal women.

Remember that after menopause, estrogen levels typically drop, but adipose tissue converts androstenedione to estrone, which is a weak estrogen.

Finally, you shouldn’t forget the influence of race in breast cancer:

Caucasians are at the highest risk while people of African descent are at increased risk for the development of triple-negative breast cancer.

Alternatively, risk factors for breast cancer in men include BRCA2 mutation and Klinefelter syndrome.

In terms of screening and diagnosis, according to the American Cancer Society guidelines, women aged 45-54 years should also undergo screening mammography every year.

If a breast mass is palpated during physical exam, a woman should undergo mammography which is the initial imaging technique used for palpable breast lesions in women older than 35 years.

Clinicians can also use needle biopsy to evaluate suspicious breast lesion since this is the most specific diagnostic tool.

As far as the treatment goes, breast cancer is treated with surgery, radiation therapy, and systemic therapy.

Surgical management of breast cancer can be performed as a radical mastectomy, which stands for removal of one or both breasts; or breast-conserving, which stands for removal of cancerous tissue while avoiding mastectomy.

Chemotherapy agents include trastuzumab, a monoclonal antibody against HER-2/neu receptors and tamoxifen, which is a selective estrogen receptor modulator.

Finally, aromatase inhibitors like anastrozole can also be used to treat estrogen receptor positive breast cancers in postmenopausal individuals.

Now breast cancer can be subdivided into non-invasive and invasive breast cancers.

First, let’s start with non-invasive breast cancers.

Now, remember that at the time when they are found, they have not crossed the basement membrane and invaded other tissue.

These include ductal carcinoma in situ, Paget disease of the breast, and lobular carcinoma in situ.

Ductal carcinoma in situ, or DCIS, is a precancerous lesion characterized by a mass of neoplastic cells that arise from epithelial cells in the terminal duct lobular unit.

As they proliferate, neoplastic cells fill the lumen of the duct, but at the same time, they do not invade into the basement membrane, which is why they are “in situ”.

In most cases, DCIS affects only one ductal system; but in some individuals, it can present as a more extensive lesion that spread to surrounding breast tissue.

In addition, DCIS accounts for 15-30% of all carcinomas found on screening mammograms; and 50% of all carcinomas identified on diagnostic mammograms.

Now there are two subtypes of ductal carcinoma in situ: comedo DCIS and non-comedo DCIS.

Comedo DCIS, also referred to as comedocarcinoma, is associated with solid sheets of pleomorphic, high-grade malignant cells, which indicate that this cancer is growing rapidly.

Moreover, central malignant cells can die and result in central necrosis, which can eventually calcify and form dystrophic calcifications.

Additional findings can include chronic inflammation and periductal concentric fibrosis.

Finally, if left untreated, malignant cells can eventually penetrate the basement membrane and invade the surrounding breast tissue, forming a poorly defined palpable breast nodule.

So for your exam, you have to remember that comedocarcinoma typically does not produce a mass lesion unless it has invaded the surrounding breast tissue; instead, it’s most commonly identified as microcalcification clusters on mammography.

In contrast to comedo DCIS, non-comedo DCIS is not associated with central necrosis and it’s subdivided into three types: papillary and micropapillary DCIS, which are characterized by malignant cells that are arranged in a finger-like pattern within the duct; cribriform DCIS, which is characterized by gaps between malignant cells; and solid DCIS, where cancer cells completely fill the duct.

The next non-invasive breast malignant condition is Paget disease of the breast!

Paget disease occurs when ductal carcinoma, either in situ or invasive, extends up to the lactiferous ducts and into the nipple and areola.

So, you have to know that women with this condition typically present with an eczematous skin lesion or persistent dermatitis in the nipple and adjacent areas.

The diagnosis of Paget disease of the breast is established by obtaining a biopsy, but women with Paget disease must undergo mammography to detect the presence of underlying breast cancer.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Variation of Breast Cancer Risk Among BRCA1/2 Carriers" JAMA (2008)
  4. "Diagnostic value of vacuum-assisted breast biopsy for breast carcinoma: a meta-analysis and systematic review" Breast Cancer Research and Treatment (2010)
  5. "Estrogen and progesterone receptors in breast cancer" Future Oncology (2014)
  6. "Ductal carcinoma in situ of breast: update 2019" Pathology (2019)