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breast cancer screening
 Breast cancer is the most common form of cancer in women.
 There are 200,000 new cases of breast cancer each year, resulting in 47,000 deaths per year.
 The lifetime risk of breast cancer is one in eight for a woman who is age 20.
 For patients under age 60, the chance of being diagnosed with breast cancer is 1 in about 400 in a given year.
 Fibrocystic change - macro Epithelial Hyperplasia
fibroadenoma   this is shown nicely in the picture on the right; the node is labeled with an " N" and the afferent lymphatic which drains the breast into this lymph node is labeled with an " L").
 notice the size difference             some flap used during the reconstructive part
Patient Age
The likelihood of certain conditions depends mainly upon age. Most breast disorders whether benign or malignant can occur in women of any age, but certain patterns are well known:
15 - 30: fibroadenomas (benign)
30 - 45: fibrocystic changes (benign)
45 - menopause : breast cysts (benign)
After menopause: cancer more likely
I. Pathophysiology
A. The etiology of breast cancer remains unknown,
but two breast cancer genes have been cloned?
the BRCA-1 and the BRCA-2 genes.
Only 10% of all of the breast cancers can be explained by mutations in these genes.
B. Estrogen stimulation is an important promoter of breast cancer.
Early menarche and late menopause are risk factors for breast cancer.
Late age at birth of first child or nulliparity also increase the risk of breast cancer.
C. Family history of breast cancer in a first degree relative and history of benign breast disease also increase the risk of breast cancer.
Recommended Intervals for Breast Cancer Screening Studies
Age <40 yr 40-49 yr 50-75 yr
Breast Self-
Examination Monthly by age 30 Monthly Monthly
Professional
Breast Examination Every 3 yr,
 ages 20-39
 Annually Annually
Mammography,
Low Risk Patient Annually Annually
Mammography,
High Risk Patient Begin at 35 yr Annually Annually
MANAGEMENT OF A MAMMOGRAPHICALLY SUSPICIOUS, NON-PALPABLE LESION. A negative core or FNA should not dissuade biopsy of a mammographically highly suspicious lesion, particularly a spiculated or stellate mass. Conversely, abnormalities that can be safely followed mammographically are not biopsied.
Method of biopsy depends on available facilities. The various biopsy methods are as follows:
 Needle-directed (guide wire directed) excisional biopsy
 The gold standard
 Facilities are widely available
 Most invasive method
 Questionable area is completely excised or at least extensively sampled
 Core needle biopsy
 Tissue obtained via a 14 gauge needle is interpretable by widely available pathologists
 Less invasive than needle-directed excisional biopsy but more so than fine needle aspiration
 The lesion is followed if the biopsy is benign and
 unless it is mammographically very suspicious
 or if the patient desires removal
 A cancer may be underdiagnosed because the lesion is not removed
 Fine needle aspiration
 Least traumatic since the sample is obtained via a 23 gauge needle
 Sample interpretation requires specialized expertise
 The lesion is followed if the biopsy is benign and
 unless it is mammographically very suspicious
 or if the patient desires removal
 A cancer may be underdiagnosed because the lesion is not removed
Localization can be obtained either stereotaxically or by ultrasound
 Stereotaxic localization
 Requires special equipment and is time consumming
 Almost all mammographically identified lesions, including microcalcifications can be localized
 If biopsies are done, each biopsy of the lesion requires a separate puncture
 Ultrasound localization
 Equipment is widely available and localization takes little time
 Not all lesions seen on mammograms can be visualized with ultrasound
 Imaging is in real time so the needle can be seen to actually enter the lesion
 Multiple areas of the lesion can be sampled through the same puncture
Comments:
 Non-mass lesions consisting of fewer than 30 microcalcifications are most reliably treated by needle-directed excisional biopsy unless all are removed because the sensitivity is about 85% in such instances.
 Contrast usually is taken up and disappears rapidly from breast cancers which can distinguish cancers from benign lesions on MRI. Biopsy can be avoided in most lesions that are not rapidly enhancing on MRI.
Algorithm:
 Mass seen on ultrasound
 Simple cyst. Mammogram in one year or aspirate.
 Cyst with debris. Aspirate for cytology
 Solid. FNA
 Unsatisfactory. Core or surgical excision.
 Benign. Repeat ultrasound in 3 months and ultrasound or mammogram in 1 and 2 years unless patient wants it excised.
 Malignant. Surgical excision.
 Mass not seen on ultrasound. Stereotaxic core or surgical excision. Mammogram in 6, 12, and 24 months if the core is benign.
 Calcifications
 Fewer than 30. Surgical excision unless all can be removed by multiple stereotaxic cores. (note: sensitivity of 85% is reported for the usual stereotaxic biopsy.)
 30 or more calcifications. Stereotaxic core.
 Architectural distortion. Surgical excision.
Note:
1. Lesions diagnosed as atypical hyperplasia on core biopsy should be surgically excised.
2. Lesions diagnosed as in situ cancer should be surgically excised and histologically examined to determine if there is an invasive element.
    peau d'orange way of the peau dorange formation every thing is in the understanding the anatomy
before and after treatment
II. Diagnosis and evaluation
A. Clinical evaluation of a breast mass
should assess
 the duration of the lesion,
 associated pain,
 relationship to the menstrual cycle or exogenous
 hormone use,
 and change in size since discovery.
 The presence of nipple discharge and its character
 bloody
 or tea-colored,
 unilateral or bilateral,
 spontaneous or expressed) should be assessed.
B. Menstrual history.
 The date of last menstrual period,
 age of menarche,
 age of menopause
 or surgical removal of the ovaries,
 regularity of the menstrual cycle,
 previous pregnancies,
 age at first pregnancy,
 lactation history should be determined.
C. History of previous breast biopsies,
 breast cancer,
 or cyst aspiration
should be investigated.
Previous or current hormone replacement therapy
Breast Cancer Screening
and dates and results of previous mammograms should be ascertained.
D. Family history should document breast cancer in relatives and the age
at which family members were diagnosed.
III.Physical examination[see self examination on breast exploration]
A. The breasts should be inspected for
 asymmetry,
 deformity,
 skin retraction,
 erythema,
 peau d'orange (indicating breast edema),
 and nipple retraction,
 discoloration,
 or inversion.
B. Palpation
1. The breasts should be palpated while the patient is sitting and then supine with the ipsilateral arm extended.
The entire breast should be palpated systematically.
2. The mass should be evaluated for
 size,
 shape,
 texture,
 tenderness,
 and fixation to skin or chest wall.
 The location of the mass should be documented with a diagram in the chart.
 The nipples should be expressed to determine whether discharge can be induced.
 Nipple discharge should be evaluated for single or multiple ducts, color, and any associated mass.
3. The axillae should be palpated for adenopathy.
 Enlarged lymph nodesshould be assessed for
 size,
 number,
 and fixation.
 The supraclavicular and cervical nodes should also be assessed.
IV.Breast imaging[see in exploration for the details]
A. Mammography
1. Screening mammography
is performed in the asymptomatic patient and consists of two views.
 Patients are not examined by a,mammographer.
 Screening mammography reduces mortality from breast cancer and should usually be initiated at age 40.
2. Diagnostic mammography
 is performed after a breast mass has been detected.
 Patients usually are examined by a mammographer, and films are interpreted immediately and additional views of the lesion are completed.
 Mammographic findings predictive of malignancy include spiculated masses with architectural distortion and microcalcifications.
 A normal mammography in the presence of a palpable mass does not exclude malignancy.
B. Ultrasonography
 is used as an adjunct to mammography to differentiate solid from cystic masses.
 It is the primary imaging modality in patients younger than 30 years old.
V. Methods of breast biopsy
A. Stereotactic core needle biopsy.
 Using a computer-driven stereotactic unit,
 the lesion is localized in three dimensions, and an automated biopsy needle obtains samples.
 The sensitivity and specificity of this technique are 95-100% and 94-98%, respectively.
B. Palpable masses. Fine-needle aspiration biopsy (FNAB)
 has a sensitivity ranging from 90-98%. Nondiagnostic aspirates require surgical biopsy.
1. The skin is prepped with alcohol and the lesion is immobilized with the nonoperating hand.
 A 10 mL syringe, with a 18 to 22 gauge needle, is introduced in to the central portion of the mass at a 90? angle.
 When the needle enters the mass, suction is applied by retracting the plunger, and the needle is advanced.
 The needle is directed into different areas of the mass while maintaining suction on the syringe.
2. Suction is slowly released before the needle is withdrawn from the mass.
 The contents of the needle are placed onto glass slides for pathologic examination.
Breast Cysts
C. Nonpalpable lesions
1. Needle localized biopsy
a. Under mammographic guidance, a needle and hookwire are placed into the breast parenchyma adjacent to the lesion.
The patient is t aken to the operating room along with mammograms for an excisional breast biopsy.
b. The skin and underlying tissues are infiltrated with 1% lidocaine with epinephrine.
 For lesions located within 5 cm of the nipple, a periareolar incision may be used or use a curved incision located over the mass and parallel to the areola.
 The skin and subcutaneous fat are incised, then the lesion is palpated and the mass is excised.
c. After removal of the specimen, a specimen x-ray is performed to confirm that the lesion has been removed.
The specimen can then be sent fresh for pathologic analysis.
d. The subcutaneous tissues should be closed with a 4-0 chromic catgut suture, and the skin should be closed with 4-0 subcuticular suture.
Breast Cysts
I. Clinical evaluation
A. A breast cyst is palpable as a smooth, mobile, well-defined mass.
 If thecyst is tense, the texture may be very f irm, resembling a cancer.
 Aspiration will determine whether the lesion is solid or cystic.
 Breast cyst fluid may vary from straw-colored to dark green.
 Cytology is not routinely necessary.
 The cyst should be aspirated completely.
B. If a mass remains after drainage or if the fluid is bloody, excisional biopsy is indicated.
 If no palpable mass is felt after drainage, the patient should be reexamined in 3-4 weeks to determine whether the cy st recurs.
 Recurrent cysts can be re-aspirated.
 Repeated recurrence of the cyst requires an open biopsy to exclude intracystic tumor.
C. Nonpalpable cysts.
If the cyst wall is seen clearly seen on ultrasound and there is no interior debris or intracystic tumor, these simple cysts do not need to be aspirated.
 Any irregularity of the cyst wall or debris within the cyst requires a needle localized biopsy.
Fibroadenomas
I. Clinical evaluation
A. Fibroadenomas frequently present in young women as
 firm,
 smooth,
 lobulated masses that are highly mobile.
 They have a benign appearance on mammography and are solid by ultrasound.
B. A tissue diagnosis can be obtained by fine needle aspiration biopsy or excisional biopsy.
II. Management of fibroadenomas
A. Fibroadenomas may be followed conservatively after the diagnosis has been made. If the mass grows, it should be excised.
B. Large fibroadenomas (>2.5 cm) should usually be excised. Often
Breast Cancer
 fibroadenomas will grow in the presence of hormonal stimulation, such as pregnancy.
Breast Cancer
 The initial management of the breast cancer patient consists of assigning a clinical stage based on examination.
 The stage may be altered once the final pathology of the tumor has been determined.
 Staging of breast cancer is based on the TNM staging system.
I. Preoperative staging in stage I and II breast cancer.
Preoperative workup should include a
 CBC,
 SMA18,
 and chest x-ray.
 If elevated alkaline phosphatase or hypercalcemia is present, a bone scan should be completed.
 Abnormal liver function tests should be investigated with a CT scan of the liver.
AmeriStages of breast cancer
Carcinoma in situ
Stage I
Stage II
Stage III
Stage IV
Inflammatory breast cancer
Recurrent
 STAGE EXPLANATION
Stages of breast cancer
 Once breast cancer has been found, more tests will be done to find out if the cancer has spread from the breast to other parts of the body.
 This is called staging. To plan treatment, a doctor needs to know the stage of the disease.
 The following stages are used for breast cancer.
Carcinoma in situ
 About 15% to 20% of breast cancers are very early cancers. They are sometimes called carcinoma in situ. There are two types of breast cancer in situ.
 One type is ductal carcinoma in situ (DCIS; also known as intraductal carcinoma); the other type is lobular carcinoma in situ (LCIS). LCIS is not cancer, but for the purpose of classifying the disease, it is called breast cancer in situ, carcinoma in situ, or stage 0 breast cancer.
 Sometimes LCIS is found when a biopsy is done for another lump or abnormality found on the mammogram.
 Patients with this condition have a 25% chance of developing breast cancer in either breast in the next 25 years.
Stage I
 The cancer is no larger than 2 centimeters (about 1 inch) and has not spread outside the breast.
Stage II
 Any of the following may be true:
 The cancer is no larger than 2 centimeters but has spread to the lymph
 nodes under the arm (the axillary lymph nodes).
 The cancer is between 2 and 5 centimeters (from 1 to 2 inches). The cancer
 may or may not have spread to the lymph nodes under the arm.
 The cancer is larger than 5 centimeters (larger than 2 inches) but has
 not spread to the lymph nodes under the arm.
Stage III
 Stage III is divided into stages IIIA and IIIB.
 Stage IIIA is defined by either of the following:
 The cancer is smaller than 5 centimeters and has spread to the lymph nodes
 under the arm, and the lymph nodes are attached to each other or to
 other structures.
 The cancer is larger than 5 centimeters and has spread to the lymph
 nodes under the arm.
 Stage IIIB is defined by either of the following:
 The cancer has spread to tissues near the breast (skin or chest wall,
 including the ribs and the muscles in the chest).
 The cancer has spread to lymph nodes inside the chest wall along the breast
 bone.
Stage IV
 The cancer has spread to other organs of the body, most often the bones, lungs, liver, or brain.
 Or, tumor has spread locally to the skin and lymph nodes inside the neck, near the collarbone.
Inflammatory breast cancer
 Inflammatory breast cancer is a special class of breast cancer that is rare.
 The breast looks as if it is inflamed because of its red appearance and warmth.
 The skin may show signs of ridges and wheals or it may have a pitted appearance. Inflammatory breast cancer tends to spread quickly.
Recurrent
 Recurrent disease means that the cancer has come back (recurred) after it has been treated. It may come back in the breast, in the soft tissues of the chest (the chest wall), or in another part of the body.
cStages
Stage 1
Tumor <=2 cm with no lymph node metastasis
Stage 2
Tumor >2 cm or positive lymph nodes
Stage 3
Locally advanced Breast Cancer (Skin or Chest wall)
Stage 4
Metestatic Breast Cancer (Lung, Liver, Bones, Brain)
Prognosis
Stage 1:
Five year survival: 90%
Stage 2
Five year survival: <60%
Seven Year survival
One to three Nodes Positive: 60%
Over 3 Nodes Positive: 38%
an Joint Committee on Cancer TNM staging for breast cancer
Methods
Axillary Node dissection
Conventional staging procedure
Complications
Numbness in axillae
Hand and arm Lymphedema (may be severe)
Sentinel Node Breast Biopsy
Major Risk Factors
Female Gender: 75% have no other known risk factors
Age related Breast Cancer Incidence in women
Age 25 years = 1:19608 risk
Age 30 years = 1:2525 risk
Age 35 years = 1:622 risk
Age 40 years = 1:217 risk
Age 45 years = 1:93 risk
Age 50 years = 1:50 risk
Age 55 years = 1:33 risk
Age 60 years = 1:24 risk
Age 65 years = 1:17 risk
Age 70 years = 1:14 risk
Age 75 years = 1:11 risk
Age 80 years = 1:10 risk
Age 85 years = 1:9 risk
Lifetime = 1:8 risk
Other Risk Factors
History of Breast Cancer
Personal History
Inversely related to Age
Risk: 0.5% - 1% per year for at least 15 years
Family History relative risk
First Degree relative: 2.3 relative risk
Unilateral/Postmenopause: 1.2 relative risk
Unilateral/Premenopause: 1.8 relative risk
Bilateral/Postmenopause: 4.0 relative risk
Bilateral/Premenopause: 8.8 relative risk
Second Degree relative: 1.5 relative risk
Mother and Sister affected: 14.0 relative risk
References
Sattin (1985) JAMA 253
Parity
Age at first birth
Age at first birth <20 years: 1.0 relative risk
Age at first birth 20-24 years: 1.2 relative risk
Age at first birth 25-29 years: 1.6 relative risk
Age at first birth 30-35 years: 1.9 relative risk
Age at first birth >35 years: 2.4 relative risk
Nulliparous: 2.0 relative risk
Hyperplasia on Breast Biopsy
Fibrocystic breast changes: No increased risk
Hyperplasia
No atypia: 2.0 relative risk
Atypia (4% Incidence): 5.0 relative risk
Special Topics
Estrogen Replacement Therapy (>5 years of use)
Risk increased by 40% (1.4 relative risk)
Alcohol may increase risk (limit to 1 drink/month)
Reference
Colditz (1995) New Eng J Med 332:1589-93
Oral Contraceptives
No (or minimal) increased Breast Cancer risk
Reference
Swanson (1992) J Amer Med Women's Assoc 47:140-8
Elective Abortion
No increased risk of Breast Cancer
Reference
Melbye (1997) JAMA 336:81-5
Lactation
Risk decreases with 2 years of cummulative Lactation
Affects premenopausal risk (not postmenopausal risk)
Reference
Newcomb (1994) N Eng J Med 338: 81-7
 Definitions for classifying the Primary Tumor (T) are the same for clinical and pathologic staging.
 All measurements refer to the tumor's greatest dimension, and the "cm" in the measurements refers to centimeters.
 For reference: 1 inch = 2.54 cm.
TX
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Primary tumor cannot be assessed
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T0
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No evidence of primary tumor
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Tis
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Carcinoma in situ, intraductal carcinoma (DCIS), lobular carcinoma in situ (LCIS), or Paget's disease of the nipple with no tumor
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T1
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Tumor 2 cm (centimeters) or less
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T1a
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0.5 cm or less
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T1b
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More than 0.5 cm but not more than 1 cm
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T1c
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More than 1 cm but not more than 2 cm
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T2
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Tumor more than 2 cm but not more than 5 cm
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T3
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Tumor more than 5 cm
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T4
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Tumor of any size with direct extension to chest wall or skin
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T4a
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Extension to chest wall
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T4b
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Edema (including peau d'orange) or ulceration of the skin of the breast or satellite skin nodules confined to the same breast
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T4c
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Both T4a and T4b
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T4d
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Inflammatory carcinoma
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Definitions for classifying the Regional Lymph Nodes (N)
NX
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Regional lymph nodes cannot be assessed (e.g., previously removed)
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N0
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No regional lymph node metastasis
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N1
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Metastasis to movable axillary lymph node(s) on the same side
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N2
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Metastasis to axillary lymph node(s) on the same side fixed to one another or other structures
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N3
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Metastasis to internal mammary lymph node(s) on the same side
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Definitions for classifying the Distant Metastasis (M)
MX
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Presence of distant metastasis cannot be assessed
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M0
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No distant metastasis
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M1
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Distant metastasis (includes metastasis to lymph node(s) on the same side, but above the collar bone
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The various TNM classifications are then used to describe the various Clinincal stages as follows:
Stage 0
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Tis
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N0
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M0
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Stage I
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T1
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N0
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M0
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Stage IIA
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T0
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N1
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M0
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T1
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N1
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M0
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T2
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N0
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M0
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Stage IIB
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T2
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N1
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M0
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T3
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N0
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M0
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Stage IIIA
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T0
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N2
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M0
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T1
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N2
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M0
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T2
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N2
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M0
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T3
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N1
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M0
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T3
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N2
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M0
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Stage IIIB
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T4
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Any N
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M0
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Any T
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N3
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M0
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Stage IV
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Any T
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Any N
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M1
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II. Surgical options for stage I and II breast cancer
A. Breast conservation therapy (BCT)
has been shown to result in survival and local recurrence rates equivalent to modified radical mastectomy; therefore, breast conservation is the preferred therapy for stage I and II breast cancer.
 The technique includes
 lumpectomy,
 axillary lymph nodedissection,
 and breast irradiation.
1. Contraindications to BCT
a. Contraindications to radiotherapy (ie, prior breast irradiation,ongoing pregnancy)
b. Steroid-dependent collagen vascular disease
c. Tumor-breast ratio that would result in an unacceptable cosmetic result (eg, a large tumor in a small breast)
d. Diffuse, malignant microcalcifications on mammography
e. Tumor greater than 5 cm in diameter
2. Lumpectomy technique.
Incisions should be curvilinear and parallel with the nipple.
 A gross margin of 1 cm should be removed.
 The lumpectomy specimen is given immediately to the pathologist for inking and for an assessment of the gross margins.
 Subcutaneous tissue is closed, and the skin is approximated with a subcuticular suture.
3. Follow-up following BCT consists of a physical examination every 3-4 months for the first 3 years,
 every 6 months for the next 2-3 years,
 then yearly.
 A SMA18 and CBC are done at each visit and a chest x-ray is done yearly.
4. A posttreatment mammography of the treated side is done 6 months after the completion of radiotherapy, then every 6 months for the first 2 years,
followed by annual mammograms. Yearly mammography should be performed on the opposite breast.
B. Modified radical mastectomy
 consists of a total mastectomy and an axillary node dissection.
 In staging axillary lymphadenectomy, levels I and II are removed routinely.
 Reconstruction of the breast should be offered to all patients undergoing mastectomy.
 Physical examination schedule and blood work are the same as for lumpectomy.
 The chest wall should be examined for of recurrence.
 Mammography of the opposite breast should continue yearly.
III.Locally advanced breast cancer (LABC)
 consists of T3 N0 (stage IIB), IIIA, and IIIB breast cancer.
 All LABC patients should undergo staging with CBC, SMA18, bone scan, and CT scan of chest and abdomen.
A. Noninflammatory LABC.
Multimodality therapy consists of neoadjuvant chemotherapy (ie, given before surgery),
 modified radical mastectomy, radiotherapy to the chest wall,
 axilla and supraclavicular nodes, and further chemotherapy.
B. Inflammatory LABC (T4d). Inflammatory breast cancer is characterized by erythema of the skin, skin edema, warmth, tenderness, and an underlying
tumor mass.
Treatment requires aggressive multi-modality therapy.
C. Follow-up. Patients should be followed closely because they are at higher risk of local and distant recurrence.
IV.Ductal carcinoma in situ (DClS)
 consist of Tis, stage 0 lesions.
 These lesions consists of malignant ductal cells that have not penetrated the basement membrane.
 DCIS is a precursor of invasive ductal cancer.
A. Physical examination is usually normal with DCIS.
The most common presentation is suspicious microcalcifications on mammography.
DCIS can cause a nipple discharge or a palpable mass.
B. Surgical therapy
1. BCT. Lumpectomy and adjuvant radiotherapy are an alternative to mastectomy in well-localized DCIS when negative microscopic margins
can be obtained.
2. Total mastectomy, including removal of the nipple areolar complex and breast tissue, results in survival rates of 98-99%.
An axillary dissection is not done routinely because the chance of nodal involvement is only 1-2%.
Free Tissue Flaps
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Pedicle Tissue Flaps
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Is cut completely free from its donor site and then moved to a new site near or far.
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Skin, fat and muscle is cut free from its donor site and moved to near-by area.
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Blood supply is cut and the arteries and veins are reconnected in the new area.
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Blood supply is never cut, the flap remains attached to its original site by the blood vessels.
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Can be moved anywhere on the body that allows re-attachment of the blood supply.
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Can only be moved as far as the blood supply will allow.
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Includes skin, fat, and muscle.
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Includes skin, fat, and muscle.
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Works very well for breast reconstruction, can give a very nice result.
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Works very well for breast reconstruction, can give a very nice result.
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Technically a more difficult operation, usually takes longer to perform, only done by surgeons with microvascular training.
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Not as technically demanding of an operation, can usually be performed a bit quicker.
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Complications less common, but much more difficult to deal with if they occur.
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Complication rate is higher, but easier to deal with.
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