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160 SURGICAL FOUNDATIONS: ESSENTIALS OF BREAST SURGERY
differences, none of the six trials demonstrated a difference in overall survival for BCT compared with mastectomy. The trials also demonstrated several points worth mentioning.
When discussing treatment options with patients, many leantoward mastectomyto avoid any chance of local recurrence. It is important to note that mastectomy does not guaran­tee freedom from local recurrence. This is true for all stages of breast cancer. Recurrence rates after mastectomy range from 3% to 20%, dep­ending on the size of the tumor, the presence of regional metastases, and the use of systemic the­rapy. Overallthe risk ofa localrecurrence isabout the same for BCT and mastectomy. Chest wall recurrences after mastectomy tend to occur later than in-breast recurrences after breast conser­vation, although most will occur within the first 3 years after surgery for both groups.
Radiation eradicates microscopic residual foci that are present in the breast after surgery. The effects of radiation have no effect on the future risk of breast cancer. Therefore the risk of a second primary cancer in the treated breast is the same as in the contralateral breast.
The six randomized trials all demonstrated that even when local recurrence was higher (as with lumpectomy without radiation), overall survival was the same. This has been interpreted as meaning that local therapy has minimal if any effect on the risk of developing distant dis­ease. Based on this interpretation, surgeons have been increasingly willing to accept therapies that have higher rates of local recurrence, argu­ing that even if an increased number of those patients ultimately require completion mastec­tomy, overall survival would not be affected. But these trials were all individually too small to detect a small impact on overall survival.
Even if there was no difference in overall survival when comparing BCT to mastectomy, patients who had BCT and developed a local recurrence do have a worse outcome. In one matched-pair analysis, BCT patients who had a local recurrence had an overall survival of 71% compared to 81% for those who did not have a local recurrence. This in itself did not prove that prospectively preventing a local recurrence would have improved survival by this degree. It could be that the local recur­rence is a marker reflecting the propensity of the tumor to metastasize distantly. So rather than metastases developing from the recur­rence, the patients with more aggressive tumors are more likely to develop both.
So does the prevention of a local recurrence improve overall survival? Yes, as demonstrated
by the Early Breast Cancer Trialists Collabora­tive Group (ECGTCG) metaanalysis. Several of the randomized trials that established the effi­cacy of breast conservation included arms in which women underwent lumpectomy alone, without radiation, and most demonstrated that despite a significant increase in local recur­rence, there was no impact on overall survival. However, these trials did not have the power to detect a small survival advantage from the improved local control provided by radiation therapy. In addition, the morbidity and mor­tality associated with radiation therapy nega­ted some survival advantage, particularly with older methods for delivering radiation. The most recent update of the ECGTCG metaanaly­sis demonstrates that the 15-year breast cancer mortality risks were significantly lower in the patients who received radiation therapy (30.5 versus 35.9, P ¼ .002). A pooled analysis of mortality data from 13 randomized trials also showed a worse survival in women who did not receive radiation therapy, with an 8.6% excess mortality. These data clearly demon­strate that improved local control does impact survival, and women with an exceedingly high risk of in-breast recurrence with BCT com­pared to mastectomy may be better served by the latter. It also establishes that radiation is a critical component of BCT.

Patient Selection

Although the surgeon plays many roles in the management of breast cancer, one of the most important is deciding whether the patient is a good candidate for BCT or whether the patient will require a mastectomy (Box 12–2).
BOX 12–2 WORKUP TO DETERMINE SUITABILITY FOR BREAST CONSERVATION
Complete history and physical
Past medical history
Medications
Complete family history
Thorough bilateral breast
examination
Bilateral mammogram with diagnostic imaging of the cancer
Review of the histology
? Ultrasound of the primary tumor
? Magnetic resonance imaging
16112—SURGICAL MANAGEMENT OF PRIMARY BREAST CANCER
There are several absolute contraindications to breast conserving therapy, some relative con­traindications, and some factors that are not contraindications, but are wrongly thought to be. The American College of Surgeons, the American College of Radiology, the College of American Pathologists, the Society of Surgical Oncology and the Canadian Steering Commit­tee on Clinical Practice Guidelines for the Care and Treatment of Breast Cancer have devel­oped consensus standards of care for BCT. The evaluation of the breast cancer patient to determine whether she is a suitable candidate for BCT includes:
A complete history and physical examina­tion before treatment. This includes a complete past medical history, present medications, and family history of cancer.
Bilateral mammographic evaluation, with appropriate magnification views, within 3 months of surgery. The tumor size, whether the mass is associated with microcalcifications, and the extent of the calcifications within and outside the mass should be included in the report.
Accurate histologic assessment of the pri­mary tumor, including histologic subtype and hormone receptor status. Thus a core-needle biopsy or excisional biopsy rather than fine-needle aspiration is the optimum choice for making a tissue diag­nosis when BCT is considered.
The most difficult part of the evaluation is the assessment of the patient’s needs and expectations. This requires that the patient and her physician discuss the ben­efits and risks of mastectomy compared to BCT in regard to long-term sur vival, the possibility and consequence of local recur­rence, and the impact on cosmetic out­come and psychosocial adjustment.
Recently, the use of magnetic resonance imaging (MRI) to determine eligibility for BCT has become more popular. Proponents state it can more accurately determine the extent of the tumor as well as identify multicentricity. However, the use of MRI is not without contro­versy. MRI of the breast is highly sensitive, but has limited specificity (see Chapter 2). As such, MRI will detect many benign lesions that would otherwise not preclude breast conservation. MRI is also limited in its ability to detect ductal carcinoma in situ (DCIS), which is often a rea­son why negative margins are not attainable. Most importantly, many institutions have the ability to perform MRI but not the technology
to perform MRI-guided biopsy. If a woman undergoes a preoperative MRI and other lesions are detected, then she may undergo additional mammograms or ultrasound to try to identify, and biopsy, the MRI-detected lesion. However, if the mammogram and ultrasound are unable to identify the lesion and MRI-guided biopsy is not available, the woman is placed in a diffi­cult position. She can ignore the findings of the MRI and proceed with BCT (risking inc­reased recurrence) or proceed with mastectomy knowing she might have been a suitable candi­date for breast preservation. Many women nat­urally choose the latter, and even when MRI­guided biopsy is available, some women choose mastectomy rather than go through additional biopsies. Thus the use of MRI may be leading to an unnecessary increase in mastectomy rates without having a significant effect on local recurrence rates. Further prospective studies are necessary before MRI can be considered a routine part of the preoperative staging pro­cess, and a full discussion of the risks, benefits, and possible outcomes of preoperative MRI should be discussed in detail with the patient. Preoperative MRI may be a reasonable option in patients who have dense breast tissue, limit­ing the ability of mammography to detect the true extent of the cancer or second cancers, or in women with a high risk of synchronous cancers (such as women with BRCA mutations) who desire breast conservation rather than bilateral mastectomies.

Absolute Contraindications

Multicentricity is an absolute contraindication to BCT (Box 12–3). This means two or more tumors are located in separate quadrants of the
BOX 12–3 ABSOLUTE CONTRAINDICATIONS TO BREAST CONSERVING THERAPY
Patient does not desire breast
conservation therapy
Unable to receive radiation therapy
First or second trimester of pregnancy (see Chapter 22)
Collagen-vascular disease
Previous chest wall radiation
Diffuse suspicious microcalcifications on
mammography
Multicentric disease
Inability to achieve negative margins
162 SURGICAL FOUNDATIONS: ESSENTIALS OF BREAST SURGERY
breast. In patients with a known breast cancer and a suspicious lesion on either physical exa­mination or breast imaging, a biopsy should be performed on the second lesion before pro­ceeding with breast conservation, even if this means an additional procedure. Multicentri­city is not the same as multifocality, which implies multiple foci of tumor when examined histologically. This has more to do with the pattern of tumor growth. The presence of mul­tifocality is not a contraindication to BCT, as long as negative margins can be obtained. Likewise, the presence of two masses within the same quadrant may not require mastec­tomy. This may represent a dumbbell-shaped tumor. If both masses can be excised in one excision, this is acceptable if the cosmetic result is reasonable. On the other hand, performing more than one lumpectomy for multiple tumors is associated with high rates of local recurrence (>30%) and poor cosmetic outcomes.
The presence of diffuse microcalcifications on mammography, often described as extend­ing beyond one quadrant, is another contrain­dication to breast conservation. These often, but not always, represent DCIS extending beyond the invasive cancer. Unfortunately, the pathology report of the mastectomy speci­men often does not reveal extensive DCIS associated with these calcifications, which can make the surgeon and the patient ques­tion the need for the mastectomy. However, the presence of the calcifications not only may indicate more extensive disease, but also may make surveillance of the breast for local recurrence extremely difficult.
Another contraindication is a history of prior therapeutic irradiation to the breast region, which when combined with the proposed treatment would result in an excessively high total radiation dose to the chest wall. This includes women who have already been treat­ed for breast cancer in that breast with radia­tion and women who have had radiation for other reasons such as for Hodgkin’s lymphoma (Fig. 12–2). Prior radiation to other body sites is not a contraindication. Sometimes in eval­uating a patient with a history of radiation, there is a question as to the dose and exact fields used. In these cases, it is best to obtain the previous treatment record and consult with a radiation oncologist before proceeding with breast conservation.
Pregnancy in the first or second trimester is an absolute contraindication to the use of breast irradiation. It may be possible to perform breast-conserving surgery in the third
Lymph nodes
Cervical
Supraclavicular
Mediastinal
Axillary
Figure 12–2. The field of radiation (including the mantle field) for Hodgkin’s disease. (From Roses D. Breast Cancer. Philadelphia: Elsevier, 2005.)
Mantle field
trimester, deferring breast irradiation until after delivery. Breast cancer during pregnancy is discussed in more detail in Chapter 22.
Because lumpectomy and radiation go hand in hand, one must consider the morbidity of radiation therapy when one is discussing lump­ectomy with the patient. Radiation often leads to fatigue, may lead to skin changes and inflam­mation of the breast, and can result in a tempo­rary cough secondary to fibrosis of the lung. In the long term, radiation can lead to pro­longed breast edema, shrinkage of the breast or induration of the cavity, fat necrosis, exces­sive fibrosis, irradiation pneumonitis, rib frac­tures, and pleural effusion. Cardiac effects and radiation-induced secondaryneoplasms arealso a concern. These are discussed in more detail in Chapter 15. However, it is important that the surgeon be able to discuss these with the patient when presenting the choice between BCT and mastectomy. On the other hand, the surgeon must be careful not to present mastectomy as “a way to avoid radiation”; depending on the pathology results, postmastectomy radiation may still be recommended.

Relative Contraindications

Some oncologists consider connective tissue disease to be an absolute contraindication to breast conservation because many of these patients tolerate irradiation very poorly. How­ever, most consider it a relative contraindica­tion, depending on the type of connective tissue disease and the relative risks and bene­fits of therapy. Scleroderma is an absolute con­traindication. Systemic lupus erythematosus patients may also have a poor reaction to radi­ation therapy. For other types of collagen­vascular disease, such as Raynaud phenomenon, rheumatoid arthritis, Sjo¨gren’s syndrome, or polymyositis, the response to radiation has not been as severe, and these patients may still be considered for BCT.
16312—SURGICAL MANAGEMENT OF PRIMARY BREAST CANCER
The ideal candidate for breast conservation is the patient with T1 or T2 tumors and a breast large enough to encompass an adequate resection. However, this is subjective and size is not an absolute contraindication. Women with large breasts can undergo resection of a 4- or 5-cm tumor with a good cosmetic result and successfully undergo breast irradiation, although they may require radiation in the prone position to assure reproducibility of the patient set-up. Patients with large tumors who still want breast conservation may con­sider neoadjuvant chemotherapy to down­stage the tumor (see Chapter 18).
Finally, there is the question of microscopic negative margins. Often described as a con­traindication to BCT is the inability to obtain negative margins. If after a reasonable attempt at reexcision there are still diffusely positive margins, then a mastectomy is indicated. It is ideal that negative margins be obtained before proceeding to radiation, because the majority of studies have demonstrated a lower local recurrence rate with negative compared to posi­tive margins. The impact of a closemargin is less clear, and the decision whether to reexcise must be made on a case-by-case basis, taking into consideration the radiation planned and the use of systemic therapy. Close margins, which have been associated with an increased risk of recurrence in some series but not in others.

Not Contraindications

There are several features that may be associated with an increased risk of recurrence, but are not necessarily contraindications to breast conser­vation (Box 12–4). The most commonly mis­quoted contraindication is the presence of axillary nodal metastases, whether these are clinical or pathologic. Given the increased like­lihood of systemic disease when the lymph nodes are positive, the impact of local control on overall survival diminishes. In addition, the risk of chest wall recurrence after mastectomy increases with the number of positive axillary lymph nodes. This is not true for breast con­servation, possibly due to the use of radiation therapy. This is why chest wall radiation is con­sidered after a mastectomy when the axillary nodes are positive (see Chapter 15).
Age is not a contraindication to BCT; physi­ologic age and the presence of comorbid con­ditions should be the primary determinants of local therapy in older women. It is also obviously wrong to assume that an older woman would be less concerned with her physical appearance or the effects of a
BOX 12–4 VARIABLES NOT CONSIDERED TO BE CONTRAINDICATIONS TO BCT
Variables Associated with an Increased Risk of Recurrence after Breast Conservation
Tumor size
Positive or close margins
High grade
Angiolymphatic invasion
Excessive delay in radiation (>16 weeks)
Young age (may be associated with
higher grade or may be associated with surgeon willingness to compromise margins for cosmetic purposes)
Variables Associated with a Decreased Likelihood of Negative Margins but No Difference in Recurrence If Negative Margins Are Obtained
Extensive intraductal component,
defined as greater than 25% or more of the tumor composed of ductal carcinoma in situ both within and at the periphery of the margin
Lobular carcinoma
mastectomy on her sexual image. Likewise, being young is not a contraindication. Even though some series have shown a higher risk of relapse in young women (defined as either younger than 35 or 40), some of these series have also shown that younger women have worse prognosis lesions (high grade, vascular invasion, ER-negative tumors) and a greater likelihood of distant disease.
Histologic subtypes other than invasive ductal carcinoma (e.g., invasive lobular cancer) are not associated with an increased risk of breast cancer recurrence, nor is the presence of an extensive intraductal component. This is defined as an invasive cancer associated with a large compo­nent of intraductal cancer (>25%) within the tumor and in the surroundingbreast tissue. Both lobular carcinomas and noncalcified DCIS may extend beyond what is visualized on imaging studies, so it may take a wider lumpectomy or a reexcision to obtain negative margins. However, if negative margins can be obtained, then breast conservation is reasonable.
As with tumor size, tumor location must be considered on a case-by-case basis and is not in itself a contraindication to breast conservation. The surgeon should discuss with the patient the cosmetic implications of the position of the lumpectomy. Tumors in the 6-o’clock position
164 SURGICAL FOUNDATIONS: ESSENTIALS OF BREAST SURGERY
of the breast will often cause downturning of the nipple after therapy. Tumors in the superfi­cial subareolar location may require resection of the nipple-areolar complex to achieve nega­tive margins. The patient and her physician need to assess whether each resection, and the effect on cosmesis, is preferable to mastectomy and reconstruction.
Breast implants previously placed for augmen­tation are not an absolute contraindication to lumpectomy. If a lumpectomy can be performed without violating the basic principles (complete tumor excision, accurate lymphatic mapping), then radiation can be delivered to the breast using standard techniques and doses. However, capsular contracture is a risk, causing the breast to become rounded, firm, and retracted upward. The suitability of BCT in women with breast implants in part depends on how the implant was placed. For example, if the implant was placed through an axillary incision, this may impact the accuracy of sentinel lymph node biopsy. Subcutaneous implants have a higher rate of capsular contraction with radiation than subpectoral. If negative margins cannot be obtained secondary to the tumor being in close proximity to the implant (cancers sometimes invade the fibrous capsule around the implant), the implant may need to be removed.
Finally, the patient’s individual risk of devel­oping a second cancer is not a contraindication to breast conservation, although a discussion should be held with these patients of their increased risk of a second breast cancer and the potential benefits of bilateral mastectomy. Thus breast cancer patients with a strong fam­ily history of breast cancer or with a known BRCA1 or BRCA2 mutation may opt for bilat­eral mastectomy; if they are not ready for that, then unilateral mastectomy as treatment of the known cancer is not warranted if they are candidates for, and desire, BCT.
incision should ideally be placed directly over the mass. Excessive tunneling is not recom­mended because this may compromise margins and make a reexcision for positive margins unnecessarily difficult. Circumareolar incisions result in a superb cosmetic outcome and are appropriate for lesions located near the areola, but care should be taken in tunneling too far simply to use a circumareolar incision.
In the upper hemisphere of the breast, inci­sions should be curvilinear, following the nor­mal lines of tension in the skin (Fig. 12–3). It is not necessary to routinely excise skin with the specimen; however, if the tumor is close to the skin, an ellipse over the tumor should be taken to ensure a negative anterior margin. In the lower hemisphere of thebreast, either cur­vilinear incisions or radial incisions can be used. For small tumors in relatively larger breasts, where it will not be necessary to remove over­lying skin and adequate breast parenchyma will remain around the cavity, curvilinear

Operative Management of Breast Cancer

Lumpectomy

Placement of the Incision
Lumpectomy may be performed either under general anesthesia or intravenous sedation with local anesthesia. The patient is placed supine on the operating room table and the entire breast and axilla is prepped and draped in an aseptic fashion. For a lumpectomy, the
Figure 12–3. Planning the lumpectomy incision. Skin incisions should be placed within the Langer’s lines when possible. Closer to the areola, circumar­eolar incisions are appropriate, but excessive tunnel­ing should be avoided. In the lower hemisphere of the breast, radial incisions should be strongly con­sidered, because these result in less distortion of the nipple-areolar complex. (From Roses D. Breast cancer. Philadelphia: Elsevier, 2005.)
16512—SURGICAL MANAGEMENT OF PRIMARY BREAST CANCER
incisions are acceptable. Otherwise, radial inci­sions should be used. Curvilinear incisions beneaththe areola,where skinor a goodamount of breast tissue is removed, will distort the breast in a way that the breast collapses inferiorly and the nipple points downward, resulting in an unacceptable cosmetic outcome. However, one must keep in mind how this would ultimately impact a mastectomy incision (particularly a skin-sparing mastectomy incision) in case the attempt at breast conservation fails (Fig. 12–4). The decision to use circumareolar or radial inci­sions in the lower hemisphere of the breast must be individualized to the patient, taking into account the size of the tumor, the size of the breast, and the pathology.
When the cancer is located in the upper outer quadrant of the breast, it may seem attractive to perform the sentinel lymph node biopsy or the axillary lymph node dissection through one longer incision. Even though this may be acceptable when the tumor lies high in the axillary tail of the breast, it should generally be avoided. It may result in a long suture line across normal skin creases, which leads to excess contraction and deformity. In addition, it complicates the planning and delivery of a boost to the tumor bed for the radiation oncologist. Thus two separate incisions for the lumpectomy and for the axilla are preferable, even if they are only 2 to 3 cm apart.
Lumpectomy
After creation of the skin incision, skin flaps are raised over the tumor. It is important that these skin flaps not be too thin. Thin flaps will result in excessive retraction of the cavity dur­ing radiation, resulting in a concavity at the site of the lumpectomy. On the other hand, thick flaps heal much better. The subcutane­ous fat helps support the skin, and if left intact, helps preserve the natural contour of the breast ( Fig. 12–5). For deep-seated tumors, after incising the skin, the breast tissue may be divided straight down to approximately 1 cm above the tumor mass before beginning the dissection around the tumor. For interme­diate masses, the skin flaps should be created at a 45-degree angle. For more superficial lesions, an adequate amount of skin overlying the tumor should be taken so that thin skin flaps are not necessary for adequate margins.
Once appropriate flaps are raised peripher­ally around the tumor, the dissection should continue straight down toward the chest wall. The surgeon should keep one hand on the tumor at all times during the dissection to ensure adequate margins. A rim of normal breast tissue or fat of approximately 1 cm should be excised with the tumor centered in the specimen. The incision should be large enough to allow this. Removing a tumor
Figure 12–4. As with exci­sional biopsies, a subsequent mastectomy should be consid­ered if the attempt at breast conservation fails. (From Bland KI, Copeland EM III. The breast, 3rd ed. Philadelphia: WB Saun­ders, 2004.)
AB
C
166 SURGICAL FOUNDATIONS: ESSENTIALS OF BREAST SURGERY
manipulation results in ink approximating the cancer, and a pathologic finding of a positive margin, necessitating reexcision. When needed, a clamp can be used to grasp the normal tissue around the mass to assist in retraction, but care should be taken not to pull too aggressively. A clamp should never be placed directly on the tumor.
scalpel, scissors, or cautery. Many surgeons prefer cautery to maintain hemostasis through­out the dissection, increasing visibility. How­ever, the cautery effect on the specimen may obscure the ability of the pathologist to read the margins. Sharp dissection results in a clearer margin status and, with appropriate technique and retraction, bleeding can be kept to a minimum. Additional time can be taken once the specimen is out to ensure hemostasis.
pectomy cavity, it is important to note and maintain its orientation. Marking sutures are immediately placed on the specimen. A single stitch superiorly, a long stitch laterally, and a double stitch deep is an easily recalled method
Figure 12–5. Preserving the subcutaneous fat between the skin and the tumor helps avoid exces­sive skin retraction and indentation. (From Bland KI, Copeland EM III. The breast, 3rd ed. Philadelphia: WB Saunders, 2004.)
to orient the tissue the same way each time, and preprinted stickers can be created for the circulating nurse (Fig. 12–6).
the adequacy of any margin, an additional
specimen can be taken from the wall of the through a small incision requires excessive manipulation of the tumor and an increased risk of positive margins on final pathology. Limiting yourself in an attempt to keep the incision small increases the need for a reexci-
lumpectomy cavity corresponding to the point
opposite the area of concern. With the skin
retracted anteriorly, the wall is grasped with
a toothed pick-up or clamp and a new, ade-
quate margin is obtained. This should be sion lumpectomy, which will have a worse cos­metic outcome than if the skin incision was simply lengthened. Excising even a small ellipse of skin with the tumor often allows for a wider operative field to work in. As the mass is freed peripherally, the tumor is grasped and retracted upward so that the posterior aspect may be completed. Exposure is aided by using small retractors. For deeper tumors, the pectoralis fascia should be included in the specimen. A portion of the pectoralis muscle should be included for very deeply situated tumors to ensure an adequate deep margin.
By working peripherally around the tumor and waiting until the tumor is circumferen­tially free to grasp the mass, the surgeon avoids excessive manipulation of the tumor. This is important because increased manipu­lation increases the likelihood of removing surrounding fat and tissue from the cancer. Exposing the tumor through excess
Figure 12–6. The lumpectomy specimen should be oriented in three planes so that the pathologist can use a multicolor staining system to identify close or positive margins.
The lumpectomy may be performed with a
As the tissue is removed from the lum-
If there is any concern clinically regarding
Short stitch:
superior
Double stitch:
deep (posterior)
Long stitch:
lateral
16712—SURGICAL MANAGEMENT OF PRIMARY BREAST CANCER
liberal, taking a generous portion of the wall of the cavity to ensure the margin of concern is truly excised. Otherwise, the pathologist may state that you obtained negative margins, but in reality left behind a close or positive mar­gin. The new specimen should be marked appropriately with sutures so that the patholo­gist knows what the true margin is.
Wound Closure
After completion of the lumpectomy, hemosta­sis should be achieved to avoid a hematoma. Drains are never used after a lumpectomy. The surgeon should also never try to simply reap­proximate the breast tissue. For large defects, there are methods to mobilize adjacent tissue (see later), but in general sutures should not be placed in the breast parenchyma to close the cavity. The lumpectomy cavity will fill with ser­oma and fibrin, and ultimately fibrous tissue, which maintains the normal, rounded contour of the breast.
Once hemostasis is achieved, surgical clips should be placed within the lumpectomy cavity in the six anatomic locations (anterior, poste­rior, medial, lateral, superior, inferior). This helps in the planning of the radiation therapy, specifically if a boost is planned or if partial breast irradiation is contemplated. The incision should then be reapproximated with absorb­able deep dermal sutures followed by a subcuti­cular stitch or tissue adhesive. Interrupted nylon or silk sutures leave cross-hatching scars and are not necessary.
Wire-Localized Lumpectomy
With the increased use of screening mammogra­phy, many cancers are diagnosed by means of a stereotactic core biopsy of a mammographic abnormality. In these cases, a wire-localized lumpectomy will be necessary. Localization involves placing a rigid introducer needle with a flexible hooked wire inside of it at the site of the abnormality using either biplanar mam­mography or ultrasound (Fig. 12–7). Ultrasound is relatively simpler and more comfortable for the patient. In many cases, the original abnor­mality is gone, removed by the core-needle biopsy, and so a clip left by the radiologist is localized for excision.
Once the rigid needle is in place, it is with­drawn, leaving the hooked wire in place. The hook keeps the wire in place so it is not easily moved, although the external wire should still be secured to the skin so that it is not
dislodged as the patient travels from radiology to the operating room. The craniocaudal and mediolateral views of the wire in place accom­pany the patient to the operating room.
The wire-localized lumpectomy is similar to the wire-localized biopsy except the surgeon is attempting to obtain negative margins. In some cases, more than one wire may be placed to bracket the mass or calcifications to give the surgeon a better idea of what needs to be excised to obtain negative margins. As with standard lumpectomy, an adequate skin inci­sion should be used to allow adequate room to excise the entire region and not overly manipulate the tissue. The incision should be curvilinear in Langer’s lines, and created with a subsequent lumpectomy or mastectomy in mind. The incision should be placed over the abnormality and not routinely made at the site of wire entry. The surgeon should use the wire and images to determine the site of the abnormality and place the incision directly over this.
The direction of the dissection is determined by the lesion size, direction of the wire, and the relative proximity of the wire to the lesion (Fig. 12–8). Wires placed just posterior to the lesion are helpful because the surgeon removes the lesion by staying deep to the localization needle. Once the incision is made, it is then necessary to identify the shaft of the lesion and retract it into the wound. Dissection in the plane facing the wire entry site allows for simple detection of the wire. Once identified, it is secured at the site of the parenchyma and the distal end of the wire is brought out into the wound. Failure to adequately secure the wire may result in accidental dislodgment. Once out, the tissue is grasped with an Allis clamp. It is preferable to grab the tissue near the wire but not the wire itself because pulling too hard on the clamp may pull the wire from the specimen. Resection of the tissue sur­rounding the wire proceeds. The relationship between the wire and the lesion, as demon­strated on mammography, helps guide how much tissue to take.
Immediately upon removal of the specimen, it is held in anatomic position and marked with orientation sutures. It is also helpful to place clips at the periphery of the specimen to allow for orientation of the specimen radiograph. These may help guide the excision of additional tissue of the lesion if there is any concern of a close radiographic margin. The specimen is sent to radiology for confirmation that the lesion in question was removed. If there is any
168 SURGICAL FOUNDATIONS: ESSENTIALS OF BREAST SURGERY
A
B
C
Figure 12–7. A and B, Mediolateral and craniocaudal views from wire localization using superior approach. C, Specimen radiograph demonstrates abnormality adjacent to the reinforced portion of the hookwire. Pathol-
ogy demonstrated ductal carcinoma in situ. (Images courtesy of Dr. Alexis Nees, Department of Radiology, University of Michigan.)
Wire has been delivered into
Hooked wire cut to manageable length
Site of wire entry into breast
Skin incision
Lesion
Nonpalpable carcinoma
Figure 12–8. The wire-localized lumpectomy. The placement of the incision and direction of the dissection are determined by the lesion size, direction of the wire, and the relative proximity of the wire to the lesion. Once the incision is made, it is best to identify the shaft of the wire and retract it into the wound. Once out, the tissue is secured and resection of the tissue surrounding the wire proceeds. (From Roses D. Breast cancer. Philadelphia: Elsevier, 2005.)
operative field
Hemostats place tension on stay suture
16912—SURGICAL MANAGEMENT OF PRIMARY BREAST CANCER
clinical concern of a close or positive margin, that should be excised as a separate specimen. The specimen radiography may also suggest a margin that appears close and requires reexci­sion. Because wire-localized lumpectomies tend to have a higher rate of close or positive mar­gins than lumpectomies for palpable masses, a more generous approach to reexcising margins at the first operation is warranted.

Reexcision Lumpectomy

Reexcision lumpectomy should be performed in any patient with unknown or positive mar­gins. It is also strongly recommended in patients with close margins, approximately 2 to 3 mm. Reexcision is necessary in one fourth to one third of lumpectomies. Failure to reexcise close or positive margins stands a high chance of leaving residual disease and increases local recurrence rates.
The standard approach to a reexcision lump­ectomy is to remove the entire cavity. An ellipse of skin is drawn around the previous skin inci­sion so that the previous scar is removed with the specimen. Skin flaps are then raised. The previous cavity is usually readily palpable, and the approach to the reexcision is similar to that of a lumpectomy. As with a lumpectomy, the surgeon should keep one hand on the cavity at all times during the dissection to ensure adequate margins. It is important not to violate
the cavity because this complicates the inking and evaluation of the new margins.
This approach is necessary when the initial lumpectomy was not oriented and inked with the six-color system. In this setting, the sur­geon does not know where the close or posi­tive margins are, so the entire cavity needs to be excised. This approach, however, results in a large volume of resected breast tissue, often beyond what is necessary to achieve negative margins. If the original lumpectomy was ori­ented and the margin in question is known, an alternative approach might be to enter the previous biopsy cavity and excise only the involved margin. This minimizes the volume of tissue excised, and studies have shown that this approach is oncologically sound, with no increased risk of local recurrence. This stresses the importance of orienting and using the six-color inking system on all breast biopsies and lumpectomies.
To reexcise just the involved margin, the previous incision may be excised completely or reopened using a scalpel. The seroma fluid is suctioned out. If too much time elapses between the original lumpectomy or biopsy and the reexcision lumpectomy, the cavity may no longer be evident. In this case, it is preferable to excise the entire cavity as described earlier. However, if there is still a cav­ity, the margin in question can be grasped at the top with an Allis forceps and that margin